Evidence map›Paper›PMID 30963920›Full record

ArticleProceedings. Biological sciences2019

Distributed plasticity in ant visual pathways following colour learning.

Ayse Yilmaz, Kornelia Grübel, Johannes Spaethe, Wolfgang Rössler

Abstract read
In one paragraph

Article in Proceedings. Biological sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Paper wasps: A model clade for social cognition.Current opinion in neurobiology · 2024
    Article
  3. Article
  4. The role of learning-walk related multisensory experience in rewiring visual circuits in the desert ant brain.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2023
    Review
  5. High diversity of arthropod colour vision: from genes to ecology.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Article
  6. Colour vision in ants (Formicidae, Hymenoptera).Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
  7. Article
  8. Article
  9. Article
  10. The neuroplasticity of division of labor: worker polymorphism, compound eye structure and brain organization in the leafcutter ant Atta cephalotes.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2020
    Article
  11. Article
  12. 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

4 authors.

Ayse YilmazDepartment of Behavioural Physiology and Sociobiology (Zoology II), Biozentrum, University of Würzburg , Am Hubland, 97074 Würzburg , Germany.
Kornelia GrübelDepartment of Behavioural Physiology and Sociobiology (Zoology II), Biozentrum, University of Würzburg , Am Hubland, 97074 Würzburg , Germany.
Johannes SpaetheDepartment of Behavioural Physiology and Sociobiology (Zoology II), Biozentrum, University of Würzburg , Am Hubland, 97074 Würzburg , Germany.
Wolfgang RösslerDepartment of Behavioural Physiology and Sociobiology (Zoology II), Biozentrum, University of Würzburg , Am Hubland, 97074 Würzburg , Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colour processing at early stages of visual pathways is a topic of intensive study both in vertebrate and invertebrate species. However, it is still unclear how colour learning and memory formation affects an insect brain in the peripheral processing stages and high-order integration centres, and whether associative colour experiences are reflected in plasticity of underlying neuronal circuits. To address this issue, we used Camponotus blandus ants as their proven colour learning and memory capabilities, precisely controllable age and experience, and already known central visual pathways offer unique access to analyse plasticity in neuronal circuits for colour vision in a miniature brain. The potential involvement of distinct neuropils-optic lobes (OLs), mushroom body (MB) input (collar) and output (vertical lobe), anterior optic tubercle (AOTU) and central complex (CX)-in associative colour experiences was assessed by quantification of volumetric and synaptic changes (MB collar) directly after colour conditioning and, 3 days later, after the establishment of long-term memory (LTM). To account for potential effects of non-associative light exposure, we compared neuronal changes in the brain of colour-naive foragers with those of foragers that had been exposed to light in a non-associative way. The results clearly show that the OLs, AOTU, and CX respond with plastic changes after colour learning and LTM formation. This suggests a complex neuronal network for colour learning and memory formation involving multiple brain levels. Such a colour-processing network probably represents an efficient design promoting fast and accurate behavioural decisions during orientation and navigation.

Indexed as

AnimalsAntsColorLearningNeuronal PlasticityNeuropilRandom AllocationVisual Pathwaysanterior optic tuberclecentral complexcolour learningmemorymushroom bodyoptic lobe

Identifiers

PMID30963920
PMCPMC6408593

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.