Evidence map›Paper›PMID 29304384›Full record

ArticlePhytochemistry2018

Diterpenoid fingerprints in pine foliage across an environmental and chemotypic matrix: Isoabienol content is a key trait differentiating chemotypes.

Astrid Kännaste, Lauri Laanisto, Leila Pazouki, Lucian Copolovici, Marina Suhorutšenko, Muhammad Azeem, Lauri Toom, Anna-Karin Borg-Karlson, Ülo Niinemets

Abstract read
In one paragraph

Article in Phytochemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Terpenoids as Potential Geroprotectors.Antioxidants (Basel, Switzerland) · 2020
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Astrid KännasteInstitute of Agricultural and Environmental Sciences, Estonian University of Life Sciences, Kreutzwaldi 1, Tartu 51014, Estonia. Electronic address: astrid.kannaste@emu.ee.
Lauri LaanistoInstitute of Agricultural and Environmental Sciences, Estonian University of Life Sciences, Kreutzwaldi 1, Tartu 51014, Estonia. Electronic address: lauri.laanisto@emu.ee.
Leila PazoukiInstitute of Agricultural and Environmental Sciences, Estonian University of Life Sciences, Kreutzwaldi 1, Tartu 51014, Estonia; Department of Biology, University of Louisville, Louisville, KY 40292, USA. Electronic address: leila.pazouki@emu.ee.
Lucian CopoloviciInstitute of Agricultural and Environmental Sciences, Estonian University of Life Sciences, Kreutzwaldi 1, Tartu 51014, Estonia; Institute of Technical and Natural Sciences Research-Development of "Aurel Vlaicu" University, 2 Elena Dragoi St., Arad 310330, Romania. Electronic address: lucian.copolovici@emu.ee.
Marina SuhorutšenkoInstitute of Agricultural and Environmental Sciences, Estonian University of Life Sciences, Kreutzwaldi 1, Tartu 51014, Estonia. Electronic address: marina.suhorutsenko@ut.ee.
Muhammad AzeemDepartment of Chemistry, COMSATS Institute of Information Technology, Abbottabad 22060, Pakistan; Ecological Chemistry Group, Department of Chemistry, KTH, Royal Institute of Technology, 100 44 Stockholm, Sweden. Electronic address: mazeemfsd@hotmail.com.
Lauri ToomInstitute of Technology, University of Tartu, Nooruse 1, Tartu 50411, Estonia. Electronic address: lauri.toom@ut.ee.
Anna-Karin Borg-KarlsonInstitute of Agricultural and Environmental Sciences, Estonian University of Life Sciences, Kreutzwaldi 1, Tartu 51014, Estonia; Ecological Chemistry Group, Department of Chemistry, KTH, Royal Institute of Technology, 100 44 Stockholm, Sweden; Institute of Technology, University of Tartu, Nooruse 1, Tartu 50411, Estonia. Electronic address: akbk@kth.se.
Ülo NiinemetsInstitute of Agricultural and Environmental Sciences, Estonian University of Life Sciences, Kreutzwaldi 1, Tartu 51014, Estonia; Estonian Academy of Sciences, Kohtu 6, 10130 Tallinn, Estonia. Electronic address: ylo.niinemets@emu.ee.

Funding

European Research Council 322603
6 · The paper itself

Abstract

Diterpenoids constitute an important part of oleoresin in conifer needles, but the environmental and genetic controls on diterpenoid composition are poorly known. We studied the presence of diterpenoids in four pine populations spanning an extensive range of nitrogen (N) availability. In most samples, isoabienol was the main diterpenoid. Additionally, low contents of (Z)-biformene, abietadiene isomers, manoyl oxide isomers, labda-7,13,14-triene and labda-7,14-dien-13-ol were quantified in pine needles. According to the occurrence and content of diterpenoids it was possible to distinguish 'non diterpenoid pines', 'high isoabienol pines', 'manoyl oxide - isoabienol pines' and 'other diterpenoid pines'. 'Non diterpenoid pines', 'high isoabienol pines' and 'other diterpenoid pines' were characteristic to the dry forest, yet the majority of pines (>80%) of the bog Laeva represented 'high isoabienol pines'. 'Manoyl oxide - isoabienol pines' were present only in the wet sites. Additionally, orthogonal partial least-squares analysis showed, that in the bogs foliar nitrogen content per dry mass (N

Indexed as

DiterpenesMolecular ConformationNaphtholsPhenotypePinusDiterpenesisoabienolNaphtholsChemotypic variabilityDiterpenoidsIsoabienolN contentPinus sylvestris L.Terpenoid signatures

Identifiers

PMID29304384
PMCPMC6020065

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.