Evidence map›Paper›PMID 28611605›Full record

ArticleFrontiers in behavioral neuroscience2017

Different Roles for Honey Bee Mushroom Bodies and Central Complex in Visual Learning of Colored Lights in an Aversive Conditioning Assay.

Jenny A Plath, Brian V Entler, Nicholas H Kirkerud, Ulrike Schlegel, C Giovanni Galizia, Andrew B Barron

Open access · goldAbstract read
In one paragraph

Article in Frontiers in behavioral neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Diversity of visual inputs to Kenyon cells of thebioRxiv : the preprint server for biology · 2023
    Article
  5. Visual learning in tethered bees modifies flight orientation and is impaired by epinastine.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2023
    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. Illusional Perspective across Humans and Bees.Vision (Basel, Switzerland) · 2022
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. A Novel Thermal-Visual Place Learning Paradigm for Honeybees (Frontiers in behavioral neuroscience · 2020
    Article
  17. Article
  18. Review
  19. Article
  20. 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

6 authors at 2 institutions in 4 countries.

Jenny A PlathDepartment of Biological Sciences, Macquarie UniversitySydney, NSW, Australia.
Brian V EntlerDepartment of Biological Sciences, Macquarie UniversitySydney, NSW, Australia.
Nicholas H KirkerudDepartment of Biology, University of KonstanzKonstanz, Germany.
Ulrike SchlegelDepartment of Biology, University of KonstanzKonstanz, Germany.
C Giovanni GaliziaDepartment of Biology, University of KonstanzKonstanz, Germany.
Andrew B BarronDepartment of Biological Sciences, Macquarie UniversitySydney, NSW, Australia.
University of Konstanz · DEMacquarie University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The honey bee is an excellent visual learner, but we know little about how and why it performs so well, or how visual information is learned by the bee brain. Here we examined the different roles of two key integrative regions of the brain in visual learning: the mushroom bodies and the central complex. We tested bees' learning performance in a new assay of color learning that used electric shock as punishment. In this assay a light field was paired with electric shock. The other half of the conditioning chamber was illuminated with light of a different wavelength and not paired with shocks. The unrestrained bee could run away from the light stimulus and thereby associate one wavelength with punishment, and the other with safety. We compared learning performance of bees in which either the central complex or mushroom bodies had been transiently inactivated by microinjection of the reversible anesthetic procaine. Control bees learned to escape the shock-paired light field and to spend more time in the safe light field after a few trials. When ventral lobe neurons of the mushroom bodies were silenced, bees were no longer able to associate one light field with shock. By contrast, silencing of one collar region of the mushroom body calyx did not alter behavior in the learning assay in comparison to control treatment. Bees with silenced central complex neurons did not leave the shock-paired light field in the middle trials of training, even after a few seconds of being shocked. We discussed how mushroom bodies and the central complex both contribute to aversive visual learning with an operant component.

Indexed as

central complexhoney beesmushroom bodiesoperant learningprocainevisual learning

Identifiers

PMID28611605
PMCPMC5447682
OpenAlexW2618867898

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.