Evidence map›Paper›PMID 30290771›Full record

ArticleBMC plant biology2018

Decoupling photo- and thermoperiod by projected climate change perturbs bud development, dormancy establishment and vernalization in the model tree Populus.

Päivi L H Rinne, Laju K Paul, Christiaan van der Schoot

Open access · goldAbstract read
In one paragraph

Article in BMC plant biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
4.7field-weighted citation impact, top 6% of its field
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

8 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
  3. Molecular Mechanisms of Seasonal Gene Expression in Trees.International journal of molecular sciences · 2024
    Review
  4. Review
  5. Article
  6. Evaluation of Cotton (Plants (Basel, Switzerland) · 2020
    Article
  7. A genetic framework for regulation and seasonal adaptation of shoot architecture in hybrid aspen.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  8. Article
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

3 authors at 1 institution in 1 country.

Päivi L H RinneFaculty of Biosciences, Department of Plant Sciences, Norwegian University of Life Sciences, Christian Magnus Falsens vei 18, 1432, Aas, Norway.
Laju K PaulFaculty of Biosciences, Department of Plant Sciences, Norwegian University of Life Sciences, Christian Magnus Falsens vei 18, 1432, Aas, Norway.
Christiaan van der SchootFaculty of Biosciences, Department of Plant Sciences, Norwegian University of Life Sciences, Christian Magnus Falsens vei 18, 1432, Aas, Norway. chris.vanderschoot@nmbu.no.
Norwegian University of Life Sciences · NO

Funding

Norwegian Research Council 192013 and 263117
6 · The paper itself

Abstract

backgroundThe performance and survival of deciduous trees depends on their innate ability to anticipate seasonal change. A key event is the timely production of short photoperiod-induced terminal and axillary buds that are dormant and freezing-tolerant. Some observations suggest that low temperature contributes to terminal bud initiation and dormancy. This is puzzling because low temperatures in the chilling range universally release dormancy. It also raises the broader question if the projected climate instabilities, as well as the northward migration of trees, will affect winter preparations and survival of trees.

resultsTo gauge the response capacity of trees, we exposed juvenile hybrid aspens to a 10-h short photoperiod in combination with different day/night temperature regimes: high (24/24 °C), moderate (18/18 °C), moderate-low (18/12 °C) and low (12/12 °C), and analysed bud development, dormancy establishment, and marker gene expression. We found that low temperature during the bud formation period (pre-dormancy) upregulated dormancy-release genes of the gibberellin (GA) pathway, including the key GA biosynthesis genes GA20oxidase and GA3oxidase, the GA-receptor gene GID1, as well as GA-inducible enzymes of the 1,3-β-glucanase family that degrade callose at plasmodesmal Dormancy Sphincter Complexes. Simultaneously, this pre-dormancy low temperature perturbed the expression of flowering pathway genes, including CO, FT, CENL1, AGL14, LFY and AP1. In brief, pre-dormancy low temperature compromised bud development, dormancy establishment, and potentially vernalization. On the other hand, a high pre-dormancy temperature prevented dormancy establishment and resulted in flushing.

conclusionsThe results show that pre-dormancy low temperature represents a form of chilling that antagonizes dormancy establishment. Combined with available field data, this indicates that natural Populus ecotypes have evolved to avoid the adverse effects of high and low temperatures by initiating and completing dormant buds within an approximate temperature-window of 24-12 °C. Global warming and erratic temperature patterns outside this range can therefore endanger the successful propagation of deciduous perennials.

Indexed as

Gene Expression Regulation, PlantClimate ChangeCold TemperatureFraxinusPhotoperiodPlant LeavesPlant ShootsPopulus1,3-β-GlucanasesCalloseChillingClimate changeDormancy Sphincter ComplexesEcotypeFloweringGibberellinPlasmodesmataTerminal bud

Identifiers

PMID30290771
PMCPMC6173867
OpenAlexW2894711452

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.