On the public citation graph

Ants integrate proprioception, visual context and efference copies to make robust predictions

0 signed · 45 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cne.22224openalex-snapshot
Neurons associated with the flip‐flop activity in the lateral accessory lobe and ventral protocerebrum of the silkworm moth brain
inferredcites →https://doi.org/10.1002/cne.24934openalex-snapshot
The brain of Cataglyphis ants: Neuronal organization and visual projections
inferredcites →https://doi.org/10.1007/978-3-642-69936-8openalex-snapshot
Vision in Drosophila
inferredcites →https://doi.org/10.1007/bf00622503openalex-snapshot
Das Reafferenzprinzip
inferredcites →https://doi.org/10.1007/s00359-012-0765-7openalex-snapshot
Descending brain neurons in the cricket Gryllus bimaculatus (de Geer): auditory responses and impact on walking
inferredcites →https://doi.org/10.1007/s00359-019-01316-6openalex-snapshot
Terrestrial cue learning and retention during the outbound and inbound foraging trip in the desert ant, Cataglyphis velox
inferredcites →https://doi.org/10.1016/j.cois.2016.02.009openalex-snapshot
The neurobiological basis of orientation in insects: insights from the silkmoth mating dance
inferredcites →https://doi.org/10.1016/j.cub.2013.10.014openalex-snapshot
Phase-Dependent Visual Control of the Zigzag Paths of Navigating Wood Ants
inferredcites →https://doi.org/10.1016/j.cub.2015.12.052openalex-snapshot
How Wasps Acquire and Use Views for Homing
inferredcites →https://doi.org/10.1016/j.cub.2016.06.070openalex-snapshot
Mechanosensation and Adaptive Motor Control in Insects
inferredcites →https://doi.org/10.1016/j.cub.2018.01.064openalex-snapshot
Proprioception
inferredcites →https://doi.org/10.1016/j.cub.2021.09.068openalex-snapshot
Suppression of motion vision during course-changing, but not course-stabilizing, navigational turns
inferredcites →https://doi.org/10.1016/j.cub.2022.11.059openalex-snapshot
An Intrinsic Oscillator Underlies Visual Navigation in Ants
inferredcites →https://doi.org/10.1016/j.tins.2004.03.004openalex-snapshot
Neural mechanisms for prediction: do insects have forward models?
inferredcites →https://doi.org/10.1016/j.tins.2006.11.005openalex-snapshot
New insights into corollary discharges mediated by identified neural pathways
inferredcites →https://doi.org/10.1037/h0055479openalex-snapshot
Neural basis of the spontaneous optokinetic response produced by visual inversion.
inferredcites →https://doi.org/10.1038/nature01652openalex-snapshot
Segregation of object and background motion in the retina
inferredcites →https://doi.org/10.1038/nature14446openalex-snapshot
Neural dynamics for landmark orientation and angular path integration
inferredcites →https://doi.org/10.1038/ncomms6919openalex-snapshot
Information flow through neural circuits for pheromone orientation
inferredcites →https://doi.org/10.1038/nn.3650openalex-snapshot
A temporal basis for predicting the sensory consequences of motor commands in an electric fish
inferredcites →https://doi.org/10.1038/nn.4083openalex-snapshot
Cellular evidence for efference copy in Drosophila visuomotor processing
inferredcites →https://doi.org/10.1038/s41467-017-00310-3openalex-snapshot
Sensorimotor computation underlying phototaxis in zebrafish
inferredcites →https://doi.org/10.1063/1.3141306openalex-snapshot
Neuromechanical models for insect locomotion: Stability, maneuverability, and proprioceptive feedback
inferredcites →https://doi.org/10.1093/beheco/ars051openalex-snapshot
Spontaneous formation of multiple routes in individual desert ants (Cataglyphis velox)
inferredcites →https://doi.org/10.1101/2020.08.13.249193openalex-snapshot
A lateralised design for the interaction of visual memories and heading representations in navigating ants
inferredcites →https://doi.org/10.1111/j.1420-9101.2007.01424.xopenalex-snapshot
Phenotypic plasticity of immune defence linked with foraging activity in the ant Cataglyphis velox
inferredcites →https://doi.org/10.1126/science.1120847openalex-snapshot
The Cellular Basis of a Corollary Discharge
inferredcites →https://doi.org/10.1152/jn.00399.2021openalex-snapshot
Temporal differences between load and movement signal integration in the sensorimotor network of an insect leg
inferredcites →https://doi.org/10.1242/jeb.00492openalex-snapshot
Rapid mechano-sensory pathways code leg impact and elicit very rapid reflexes in insects
inferredcites →https://doi.org/10.1242/jeb.090266openalex-snapshot
Dynamic use of optic flow during pheromone tracking by the male silkmoth, Bombyx mori
inferredcites →https://doi.org/10.1242/jeb.148213openalex-snapshot
Naturalistic path integration of Cataglyphis desert ants on an air-cushioned lightweight spherical treadmill
inferredcites →https://doi.org/10.1242/jeb.198.8.1637openalex-snapshot
Optical Scaling in Conspecific Cataglyphis Ants
inferredcites →https://doi.org/10.1242/jeb.205.16.2499openalex-snapshot
View-based navigation in insects: how wood ants (Formica rufaL.) look at and are guided by extended landmarks
inferredcites →https://doi.org/10.1242/jeb.212332openalex-snapshot
Connecting brain to behaviour: a role for general purpose steering circuits in insect orientation?
inferredcites →https://doi.org/10.1242/jeb.218701openalex-snapshot
Route-following ants respond to alterations of the view sequence
inferredcites →https://doi.org/10.21105/joss.03139openalex-snapshot
performance: An R Package for Assessment, Comparison and Testing of Statistical Models
inferredcites →https://doi.org/10.2307/3545608openalex-snapshot
Links between Worker Polymorphism and Thermal Biology in a Thermophilic Ant Species
inferredcites →https://doi.org/10.2307/4615733openalex-snapshot
A Simple Sequentially Rejective Multiple Test Procedure
inferredcites →https://doi.org/10.3929/ethz-b-000105397openalex-snapshot
Fitting Linear Mixed-Effects Models Using lme4
inferredcites →https://doi.org/10.4324/9780203780794openalex-snapshot
The Organization of Action
inferredcites →https://doi.org/10.7554/elife.15504openalex-snapshot
Continuous lateral oscillations as a core mechanism for taxis in Drosophila larvae
inferredcites →https://doi.org/10.7717/peerj.616openalex-snapshot
Using observation-level random effects to model overdispersion in count data in ecology and evolution

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1073/pnas.2410908121openalex-snapshot
Compensation to visual impairments and behavioral plasticity in navigating ants
inferred← citeshttps://doi.org/10.1242/jeb.249935openalex-snapshot
Is this scenery worth exploring? Insight into the visual encoding of navigating ants
inferred← citeshttps://doi.org/10.3389/fetho.2024.1341120openalex-snapshot
The ethology of foraging in ants: revisiting Tinbergen’s four questions
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.