Evidence map›Paper›PMID 25617469›Full record

ReviewJournal of experimental botany2015

The divining root: moisture-driven responses of roots at the micro- and macro-scale.

Neil E Robbins, José R Dinneny

Abstract readReview
In one paragraph

Review in Journal of experimental botany, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
–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

38 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Review
  4. A high-quality genome assembly reveals adaptations underlying glossy, wax-coated leaves in the heat-tolerant wild raspberry Rubus leucanthus.DNA research : an international journal for rapid publication of reports on genes and genomes · 2024
    Article
  5. Article
  6. Frontiers in microbiology · 2024
    Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Evidence for root adaptation to a spatially discontinuous water availability in the absence of external water potential gradients.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  14. Article
  15. Genome-Wide Analysis of theFrontiers in plant science · 2021
    Article
  16. Root Response to Drought Stress in Rice (International journal of molecular sciences · 2020
    Review
  17. Temporal genetic patterns of root growth in Brassica napus L. revealed by a low-cost, high-efficiency hydroponic system.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2019
    Article
  18. Article
  19. Plasticity of Lateral Root Branching in Maize.Frontiers in plant science · 2019
    Review
  20. 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

2 authors.

Neil E RobbinsCarnegie Institution for Science, Department of Plant Biology, 260 Panama Street, Stanford, CA 94305, USA Department of Biology, Stanford University, 371 Serra Mall, Stanford, CA 94305, USA.ORCID http://orcid.org/0000-0001-5534-3666
José R DinnenyCarnegie Institution for Science, Department of Plant Biology, 260 Panama Street, Stanford, CA 94305, USA jdinneny@carnegiescience.edu.ORCID http://orcid.org/0000-0002-3998-724X

Funding

Supplement to Enhance Wellness and Resiliency in the Graduate EnvironmentT32GM007276 · NIGMS · STANFORD UNIVERSITY · PI MORRISON, ASHBY J. · 1985 to 2023
$32.9M
NIGMS NIH HHS T32 GM007276
6 · The paper itself

Abstract

Water is fundamental to plant life, but the mechanisms by which plant roots sense and respond to variations in water availability in the soil are poorly understood. Many studies of responses to water deficit have focused on large-scale effects of this stress, but have overlooked responses at the sub-organ or cellular level that give rise to emergent whole-plant phenotypes. We have recently discovered hydropatterning, an adaptive environmental response in which roots position new lateral branches according to the spatial distribution of available water across the circumferential axis. This discovery illustrates that roots are capable of sensing and responding to water availability at spatial scales far lower than those normally studied for such processes. This review will explore how roots respond to water availability with an emphasis on what is currently known at different spatial scales. Beginning at the micro-scale, there is a discussion of water physiology at the cellular level and proposed sensory mechanisms cells use to detect osmotic status. The implications of these principles are then explored in the context of cell and organ growth under non-stress and water-deficit conditions. Following this, several adaptive responses employed by roots to tailor their functionality to the local moisture environment are discussed, including patterning of lateral root development and generation of hydraulic barriers to limit water loss. We speculate that these micro-scale responses are necessary for optimal functionality of the root system in a heterogeneous moisture environment, allowing for efficient water uptake with minimal water loss during periods of drought.

Indexed as

HumidityDehydrationOrgan SpecificityPlant DevelopmentPlant RootsSignal TransductionHydropatterningosmosensingplant–water relationsroot developmentroot system architecturewater stress.

Identifiers

PMID25617469
PMCPMC4817643

What OpenQuestion holds

Textmetadata
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.