Works matching IS 0028646X AND DT 2016 AND VI 211 AND IP 2
Results: 33
Cloud forest trees with higher foliar water uptake capacity and anisohydric behavior are more vulnerable to drought and climate change.
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- New Phytologist, 2016, v. 211, n. 2, p. 489, doi. 10.1111/nph.13952
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Understanding the roles of nonstructural carbohydrates in forest trees - from what we can measure to what we want to know.
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- New Phytologist, 2016, v. 211, n. 2, p. 386, doi. 10.1111/nph.13955
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Nitric oxide and S-nitrosoglutathione function additively during plant immunity.
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- New Phytologist, 2016, v. 211, n. 2, p. 516, doi. 10.1111/nph.13903
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Variation in wood nutrients along a tropical soil fertility gradient.
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- New Phytologist, 2016, v. 211, n. 2, p. 440, doi. 10.1111/nph.13904
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A computational framework for mapping the timing of vegetative phase change.
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- New Phytologist, 2016, v. 211, n. 2, p. 750, doi. 10.1111/nph.13907
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OsCLT1, a CRT-like transporter 1, is required for glutathione homeostasis and arsenic tolerance in rice.
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- New Phytologist, 2016, v. 211, n. 2, p. 658, doi. 10.1111/nph.13908
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Methane emissions from the trunks of living trees on upland soils.
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- New Phytologist, 2016, v. 211, n. 2, p. 429, doi. 10.1111/nph.13909
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The sun doesn't shine equally on everyone.
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- New Phytologist, 2016, v. 211, n. 2, p. 377, doi. 10.1111/nph.14032
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Cover and Issue Information.
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- New Phytologist, 2016, v. 211, n. 2, p. 373, doi. 10.1111/nph.13669
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- Article
Macroevolutionary patterns of ultraviolet floral pigmentation explained by geography and associated bioclimatic factors.
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- New Phytologist, 2016, v. 211, n. 2, p. 708, doi. 10.1111/nph.13921
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Evolutionary analysis of iron (Fe) acquisition system in Marchantia polymorpha.
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- New Phytologist, 2016, v. 211, n. 2, p. 569, doi. 10.1111/nph.13922
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Rice PROTEIN l-ISOASPARTYL METHYLTRANSFERASE isoforms differentially accumulate during seed maturation to restrict deleterious isoAsp and reactive oxygen species accumulation and are implicated in seed vigor and longevity.
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- New Phytologist, 2016, v. 211, n. 2, p. 627, doi. 10.1111/nph.13923
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BODYGUARD is required for the biosynthesis of cutin in Arabidopsis.
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- New Phytologist, 2016, v. 211, n. 2, p. 614, doi. 10.1111/nph.13924
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Why is gynodioecy a rare but widely distributed sexual system? Lessons from the Lamiaceae.
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- New Phytologist, 2016, v. 211, n. 2, p. 688, doi. 10.1111/nph.13926
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Plasticity in leaf-level water relations of tropical rainforest trees in response to experimental drought.
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- New Phytologist, 2016, v. 211, n. 2, p. 477, doi. 10.1111/nph.13927
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The role of phosphorus, magnesium and potassium availability in soil fungal exploration of mineral nutrient sources in Norway spruce forests.
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- New Phytologist, 2016, v. 211, n. 2, p. 542, doi. 10.1111/nph.13928
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Use of micro RNA-encoded peptide mi PEP172c to stimulate nodulation in soybean.
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- New Phytologist, 2016, v. 211, n. 2, p. 379, doi. 10.1111/nph.13991
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Characterization of photomorphogenic responses and signaling cascades controlled by phytochrome-A expressed in different tissues.
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- New Phytologist, 2016, v. 211, n. 2, p. 584, doi. 10.1111/nph.13941
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Cell cycle arrest induced by inhibitors of epigenetic modifications in maize ( Zea mays) seedling leaves: characterization of the process and possible mechanisms involved.
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- New Phytologist, 2016, v. 211, n. 2, p. 646, doi. 10.1111/nph.13942
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Macroecology of biodiversity: disentangling local and regional effects.
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- New Phytologist, 2016, v. 211, n. 2, p. 404, doi. 10.1111/nph.13943
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Terminal bacteroid differentiation in the legume−rhizobium symbiosis: nodule-specific cysteine-rich peptides and beyond.
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- New Phytologist, 2016, v. 211, n. 2, p. 411, doi. 10.1111/nph.14025
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The influence of sampled biomass on species-area relationships of grassland plants.
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- New Phytologist, 2016, v. 211, n. 2, p. 382, doi. 10.1111/nph.14028
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Compartmentalized gene regulatory network of the pathogenic fungus Fusarium graminearum.
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- New Phytologist, 2016, v. 211, n. 2, p. 527, doi. 10.1111/nph.13912
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Arabidopsis CLAVATA1 and CLAVATA2 receptors contribute to Ralstonia solanacearum pathogenicity through a miR169-dependent pathway.
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- New Phytologist, 2016, v. 211, n. 2, p. 502, doi. 10.1111/nph.13913
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ORA47 (octadecanoid-responsive AP2/ERF-domain transcription factor 47) regulates jasmonic acid and abscisic acid biosynthesis and signaling through binding to a novel cis-element.
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- New Phytologist, 2016, v. 211, n. 2, p. 599, doi. 10.1111/nph.13914
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Managing the protein folding demands in the endoplasmic reticulum of plants.
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- New Phytologist, 2016, v. 211, n. 2, p. 418, doi. 10.1111/nph.13915
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Facilitation contributes to Mediterranean woody plant diversity but does not shape the diversity-productivity relationship along aridity gradients.
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- New Phytologist, 2016, v. 211, n. 2, p. 464, doi. 10.1111/nph.13916
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Recent mating-system evolution in Eichhornia is accompanied by cis-regulatory divergence.
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- New Phytologist, 2016, v. 211, n. 2, p. 697, doi. 10.1111/nph.13918
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The homeodomain transcription factor Ta HDZipI-2 from wheat regulates frost tolerance, flowering time and spike development in transgenic barley.
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- New Phytologist, 2016, v. 211, n. 2, p. 671, doi. 10.1111/nph.13919
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Plasticity in plant functional traits is shaped by variability in neighbourhood species composition.
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- New Phytologist, 2016, v. 211, n. 2, p. 455, doi. 10.1111/nph.13935
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Colonization and diversification in the African 'sky islands': insights from fossil-calibrated molecular dating of Lychnis (Caryophyllaceae).
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- New Phytologist, 2016, v. 211, n. 2, p. 719, doi. 10.1111/nph.13937
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Light acclimation in the lycophyte Selaginella martensii depends on changes in the amount of photosystems and on the flexibility of the light-harvesting complex II antenna association with both photosystems.
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- New Phytologist, 2016, v. 211, n. 2, p. 554, doi. 10.1111/nph.13939
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Using codispersion analysis to quantify and understand spatial patterns in species-environment relationships.
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- New Phytologist, 2016, v. 211, n. 2, p. 735, doi. 10.1111/nph.13934
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