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Response to self-motion in waterstriders: visual discrimination between rotation and translation

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What this work says

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

inferredcites →https://doi.org/10.1007/bf00192580openalex-snapshot
Drift compensation and its sensory basis in waterstriders (Gerris paludum F.)
inferredcites →https://doi.org/10.1007/bf00193552openalex-snapshot
Eye specialisation in waterstriders: an adaptation to life in a flat world
inferredcites →https://doi.org/10.1007/bf00193553openalex-snapshot
Waterstriders (Gerris paludum F.) compensate for drift with a discontinuously working visual position servo
inferredcites →https://doi.org/10.1007/bf00365219openalex-snapshot
Facts on optic flow
inferredcites →https://doi.org/10.1007/bf00610732openalex-snapshot
The optomotor system on the ground: on the absence of visual control of speed in walking ladybirds
inferredcites →https://doi.org/10.1007/bf00610996openalex-snapshot
Multisensory control of eye-stalk orientation in space: crabs from different habitats rely on different senses
inferredcites →https://doi.org/10.1007/bf00613448openalex-snapshot
Distribution of optokinetic sensitivity over the eye of crabs: its relation to habitat and possible role in flow-field analysis
inferredcites →https://doi.org/10.1007/bf00613835openalex-snapshot
The optomotor equilibrium of theDrosophila navigation system
inferredcites →https://doi.org/10.1007/bf00657045openalex-snapshot
Some operating rules for the optomotor system of a hoverfly during voluntary flight
inferredcites →https://doi.org/10.1007/bf01054613openalex-snapshot
Separation of translation and rotation by means of eye-region specialization in flying gypsy moths (Lepidoptera: Lymantriidae)
inferredcites →https://doi.org/10.1242/jeb.154.1.81openalex-snapshot
Eye Movements in the Rock Crab Pachygrapsus Marmoratus Walking Along Straight and Curved Paths
inferredcites →https://doi.org/10.1242/jeb.154.1.99openalex-snapshot
Sensory Basis and Functional Role of Eye Movements Elicited During Locomotion in the Land Crab Cardisoma Guanhumi

What points at this work

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

inferred← citeshttps://doi.org/10.1007/978-3-540-89393-6_9openalex-snapshot
Insect-Inspired Odometry by Optic Flow Recorded with Optical Mouse Chips
inferred← citeshttps://doi.org/10.1007/978-3-642-56550-2_18openalex-snapshot
Towards an Ecology of Motion Vision
inferred← citeshttps://doi.org/10.1007/978-3-642-56550-2_8openalex-snapshot
Extracting Egomotion from Optic Flow: Limits of Accuracy and Neural Matched Filters
inferred← citeshttps://doi.org/10.1007/978-3-642-75869-0_16openalex-snapshot
An Eye or Ear for Flying
inferred← citeshttps://doi.org/10.1007/bf00194578openalex-snapshot
Freely flying bees discriminate between stationary and moving objects: performance and possible mechanisms
inferred← citeshttps://doi.org/10.1007/bf00195398openalex-snapshot
Flight-phase and visual-field related optomotor yaw responses in gregarious desert locusts during tethered flight
inferred← citeshttps://doi.org/10.1007/bf00196420openalex-snapshot
The response of the hovering hawk moth Macroglossum stellatarum to translatory pattern motion
inferred← citeshttps://doi.org/10.1007/bf02009505openalex-snapshot
How locusts separate pattern flow into its rotatory and translatory components (Orthoptera: Acrididae)
inferred← citeshttps://doi.org/10.1007/s003590050173openalex-snapshot
Visual position stabilization in the hummingbird hawk moth, Macroglossum stellatarum L. I. Behavioural analysis
inferred← citeshttps://doi.org/10.1016/b978-008045046-9.01976-8openalex-snapshot
Visually Guided Behavior
inferred← citeshttps://doi.org/10.1016/b978-012240530-3/50010-9openalex-snapshot
Self-Motion
inferred← citeshttps://doi.org/10.1016/j.neuron.2013.04.029openalex-snapshot
Modular Use of Peripheral Input Channels Tunes Motion-Detecting Circuitry
inferred← citeshttps://doi.org/10.1017/s0952523800005344openalex-snapshot
Interactions of local movement detectors enhance the detection of rotation. Optokinetic experiments with the rock crab, Pachygrapsus marmoratus
inferred← citeshttps://doi.org/10.1023/a:1013610201135openalex-snapshot
Catadioptric Projective Geometry
inferred← citeshttps://doi.org/10.1080/09548980500497758openalex-snapshot
Movement-induced motion signal distributions in outdoor scenes
inferred← citeshttps://doi.org/10.1098/rstb.1992.0105openalex-snapshot
What can engineers learn from insect vision?
inferred← citeshttps://doi.org/10.1109/icpr.2000.905282openalex-snapshot
Omnidirectional vision: theory and algorithms
inferred← citeshttps://doi.org/10.1109/icsmc.1993.384999openalex-snapshot
What can engineers learn from insect vision?
inferred← citeshttps://doi.org/10.1111/eth.13213openalex-snapshot
Importance of vision in tandem running during colony relocation in an Indian ant
inferred← citeshttps://doi.org/10.1111/j.1439-0310.1998.tb00069.xopenalex-snapshot
A Functionally Equivalent Artificial Neural Network Model of the Prey Orientation Behavior of Waterstriders (Gerridae)
inferred← citeshttps://doi.org/10.1146/annurev-ento-010715-023703openalex-snapshot
The Sensory Ecology of Ant Navigation: From Natural Environments to Neural Mechanisms
inferred← citeshttps://doi.org/10.1242/jeb.118299openalex-snapshot
Whole-field visual motion drives swimming in larval zebrafish via a stochastic process
inferred← citeshttps://doi.org/10.1364/ao.53.000368openalex-snapshot
Range and egomotion estimation from compound photodetector arrays with parallel optical axis using optical flow techniques
inferred← citeshttps://doi.org/10.1515/znc-1998-7-811openalex-snapshot
Sensory Ecology and Neural Coding in Arthropods
inferred← citeshttps://doi.org/10.3389/fnins.2017.00622openalex-snapshot
Visual Sensory Signals Dominate Tactile Cues during Docked Feeding in Hummingbirds
inferred← citeshttps://doi.org/10.3390/s141121045openalex-snapshot
Odometry for Ground Moving Agents by Optic Flow Recorded with Optical Mouse Chips
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