ArticleTree physiology2020
Production of constitutive and induced secondary metabolites is coordinated with growth and storage in Norway spruce saplings.
Article in Tree physiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 31 citations in OpenAlex.
- Light Limitation and Foliar Pathogenic Infection Impact Phloem Anatomy and Function in Pinus radiata D. Don.Plant, cell & environment · 2025Article
- Water, not carbon, drives drought-constraints on stem terpene defense against simulated bark beetle attack in Pinus edulis.The New phytologist · 2025Article
- Understanding the role of oxylipins inFrontiers in plant science · 2025Review
- Windthrow causes declines in carbohydrate and phenolic concentrations and increased monoterpene emission in Norway spruce.PloS one · 2024Article
- Elevated nutrient supply can exert worse effects on Norway spruce than drought, viewed through chemical defence against needle rust.Tree physiology · 2023Article
- Globally consistent response of plant microbiome diversity across hosts and continents to soil nutrients and herbivores.Nature communications · 2023Article
- Plant Secondary Metabolites: The Weapons for Biotic Stress Management.Metabolites · 2023Review
- Article
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Authors and funding
7 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
A mechanistic understanding of how trees balance the trade-offs between growth, storage and defense is limited but crucial for predicting tree responses to abiotic and biotic stresses. Here we investigated how trees allocate storage of non-structural carbohydrates (NSC) to growth and constitutive and induced secondary metabolites (SM). We exposed Norway spruce (Picea abies) saplings to 5 weeks of complete darkness to induce light and/or carbon limitation and then applied methyl jasmonate (MeJA) to simulate biotic attack. We measured changes in biomass, NSC (sum of soluble sugars and starches), and constitutive and induced SM (sum of phenolic compounds and terpenoids) in current-year developing and previous-year mature needles and branches, as well as volatiles emitted from the canopy. Under darkness, NSC storage was preferentially used for constitutive biosynthesis of monoterpenes rather than biosynthesis of stilbenes and growth of developing organs, while SM stored in mature organs cannot be remobilized and recycled. Furthermore, MeJA-induced production of SM was constrained by low NSC availability in developing organs but not in mature organs grown in the dark. Emissions of volatiles were suppressed in the dark but after 1 h of re-illumination, emissions of both constitutive and induced monoterpene hydrocarbons recovered rapidly, whereas emissions of linalool and sesquiterpene produced via de novo synthesis did not recover. Our results highlight that light and/or carbon limitation may constrain constitutive and JA-induced biosynthesis of SM in coordination with growth, NSC storage and mobilization.
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