OSCR

Anatomical Investigation Reveals a Second Olfactory System in Locusts.

Overview

Authors: Zane N Aldworth1, Brian Kim1,2, Kui Sun1, Esther Ndungu1, Vi Nguyen1, Mark A Stopfer1
ORCID iDs: Zane N Aldworth
  1. Laboratory of Cellular and Synaptic Physiology, NIH‐NICHD, Bethesda, Maryland, USA
  2. Brown University–National Institutes of Health Neuroscience Graduate Partnership Program, Providence, Rhode Island, USA
Journal: The Journal of comparative neurology, volume 534, issue 8, article e70197
Dates: received 26 November 2025; accepted 29 July 2026; published online 19 August 2026; in print August 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1002/cne.70197 · PMID 42618969 · PMCID PMC13490624 · OpenAlex W7160890571
Open access: hybrid, a free copy (OpenAlex)
Status: data only
Categories: other (organism), cellular / molecular (subfield)
Methods: Statistics
MeSH: Grasshoppers*, Olfactory Pathways*, Smell*, Animals, Brain, Female, Male, Olfactory Receptor Neurons, Sensilla (* major topic)
Topic: Neurobiology and Insect Physiology Research (Cellular and Molecular Neuroscience, Neuroscience), according to OpenAlex
Funding: Eunice Kennedy Shriver National Institute of Child Health and Human Development (1ZIAHD008760-20, 1ZIAHD008760‐20); Intramural NIH HHS (ZIA HD008760); National Institutes of Health; NIH HHS
Citations: not cited yet (Europe PMC); 104 references in the paper
Research resources: RRID:AB_143165, RRID:AB_2936984, either mouse ⍺‐GABA RRID:AB_476667, rabbit ⍺‐GABA RRID:AB_477652

Abstract

Olfaction in locusts offers a useful model for understanding how the brain encodes environmental information. While previous studies of olfaction in locusts have focused mainly on the antennal pathway, most insects, including locusts, possess olfactory receptors on their palps. Although they are traditionally considered to be gustatory or mechanosensory structures, accumulating molecular, electrophysiological, and behavioral evidence shows locust palps also mediate olfactory processing. The palps therefore initiate a second olfactory pathway, whose neural architecture and sensory functions remain largely unexplored. Here, we used anatomical approaches to characterize the chemosensory system of the palps in Schistocerca americana, mapping pathways from the peripheral sensilla through the brain to third‐order neurons. We found that sensory input from the palps projects to two distinct regions: the gnathal ganglion, which integrates gustatory input from multiple head appendages, and the glomerular lobe of the cerebral ganglion, which, traditionally thought of as a gustatory center, appears instead to receive only olfactory input. The glomerular lobe, in turn, provides olfactory input to the accessory calyx of the mushroom body, a region traditionally considered gustatory. Notably, the palp and antennal olfactory pathways remain anatomically segregated through at least the third‐order neurons. Our systematic characterization of the palp olfactory system anatomy challenges existing views of olfactory and gustatory integration in hemimetabolous insects and establishes a framework for comparative studies of antennal and palp‐based olfactory coding.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

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Data

Datasets cited

Data Availability Statement

All data supporting the findings of this study have been deposited in Zenodo and are available at https://doi.org/10.5281/zenodo.20146646. In addition, the Schistocerca americana standard brain generated for this study, as well as all individual reconstructed neurons, has been made available via the Insect Brain Database: https://www.insectbraindb.org/app/species/53.

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 3, 28 September 2026

  • Publisher: — → Wiley

Version 1, 27 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 6 authors, 9 MeSH terms, 4 funders, 99 references, 4 RRIDs.

Cite

This paper

Aldworth, Z. N., Kim, B., Sun, K., Ndungu, E., Nguyen, V., & Stopfer, M. A. (2026). Anatomical Investigation Reveals a Second Olfactory System in Locusts. The Journal of comparative neurology, 534(8), e70197. https://doi.org/10.1002/cne.70197

BibTeX

@article{aldworth2026anatomical,
author = {Aldworth, Zane N and Kim, Brian and Sun, Kui and Ndungu, Esther and Nguyen, Vi and Stopfer, Mark A},
title = {{Anatomical Investigation Reveals a Second Olfactory System in Locusts}},
journal = {The Journal of comparative neurology},
year = {2026},
month = aug,
volume = {534},
number = {8},
pages = {e70197},
publisher = {Wiley},
issn = {0021-9967},
doi = {10.1002/cne.70197},
url = {https://doi.org/10.1002/cne.70197},
pmid = {42618969},
pmcid = {PMC13490624}
}

RIS

TY - JOUR
AU - Aldworth, Zane N
AU - Kim, Brian
AU - Sun, Kui
AU - Ndungu, Esther
AU - Nguyen, Vi
AU - Stopfer, Mark A
TI - Anatomical Investigation Reveals a Second Olfactory System in Locusts
T2 - The Journal of comparative neurology
J2 - J Comp Neurol
PY - 2026
DA - 2026/08/01
VL - 534
IS - 8
SP - e70197
SN - 0021-9967
PB - Wiley
DO - 10.1002/cne.70197
UR - https://doi.org/10.1002/cne.70197
LA - en
ER -

CSL-JSON

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