Literature DB >> 8366472

Dead reckoning in a small mammal: the evaluation of distance.

V Séguinot1, R Maurer, A S Etienne.   

Abstract

When hoarding food under infra-red light, golden hamsters Mesocricetus auratus W. return fairly directly from a feeding place to their nest site by evaluating and updating internal signals that they have generated during the previous outward journey to the feeding place. To test more specifically the animals' capacity to evaluate the linear components of the outward journey, the subjects were led from their (cone-shaped) nest to a feeding place along a detour which comprised either 2 (experiment 1) or 5 (experiment 2) segments; adjoining segments were at right angles to each other. In these conditions, the subjects remained significantly oriented towards the nest and therefore were capable of assessing translations as well as rotations during the outward journey. In experiment 3, the nest was removed after the hamsters had started the direct outward journey to the feeding place and the hamsters were rotated during the food uptake. The animals were no longer oriented towards the starting point of their journey, but nonetheless covered, along a fairly straight path, the correct homing distance, and then changed over to a circular search path. These results confirm that mammals can derive the linear components of an outward journey from self-generated signals and therefore are able to judge the homing distance without relying on cues from the environment. For a number of detour outward journeys, our data yield an unexpectedly good fit to Müller and Wehner's (1988) model of dead reckoning in ants. However, this is no longer the case when the outward journey contains an initial loop which brings the subject back to the starting point. These findings are discussed in terms of the biological significance and limitations of an approximate form of path integration.

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Year:  1993        PMID: 8366472     DOI: 10.1007/bf00209622

Source DB:  PubMed          Journal:  J Comp Physiol A            Impact factor:   1.836


  5 in total

1.  Path integration in desert ants, Cataglyphis fortis.

Authors:  M Müller; R Wehner
Journal:  Proc Natl Acad Sci U S A       Date:  1988-07       Impact factor: 11.205

2.  Linear displacement can be derived from otolithic information and stored on spatial maps controlling the saccadic system.

Authors:  A Berthoz; I Israël; E Vitte; D Zee
Journal:  Adv Otorhinolaryngol       Date:  1988

3.  [Basic analysis of the effective system of homing in spider Agelena labyrinthica (Cl.)].

Authors:  K Dornfeldt
Journal:  Z Tierpsychol       Date:  1975-10

4.  Contribution of the otoliths to the calculation of linear displacement.

Authors:  I Israël; A Berthoz
Journal:  J Neurophysiol       Date:  1989-07       Impact factor: 2.714

5.  The orientation of the golden hamster to its nest-site after the elimination of various sensory cues.

Authors:  A S Etienne
Journal:  Experientia       Date:  1980-09-15
  5 in total
  14 in total

1.  Intact landmark control and angular path integration by head direction cells in the anterodorsal thalamus after lesions of the medial entorhinal cortex.

Authors:  Benjamin J Clark; Jeffrey S Taube
Journal:  Hippocampus       Date:  2010-11-03       Impact factor: 3.899

2.  Both visual and idiothetic cues contribute to head direction cell stability during navigation along complex routes.

Authors:  Ryan M Yoder; Benjamin J Clark; Joel E Brown; Mignon V Lamia; Stephane Valerio; Michael E Shinder; Jeffrey S Taube
Journal:  J Neurophysiol       Date:  2011-03-30       Impact factor: 2.714

Review 3.  Path integration, views, search, and matched filters: the contributions of Rüdiger Wehner to the study of orientation and navigation.

Authors:  Ken Cheng; Cody A Freas
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2015-02-07       Impact factor: 1.836

Review 4.  Neural mechanisms of navigation involving interactions of cortical and subcortical structures.

Authors:  James R Hinman; Holger Dannenberg; Andrew S Alexander; Michael E Hasselmo
Journal:  J Neurophysiol       Date:  2018-02-14       Impact factor: 2.714

5.  Keeping track of the distance from home by leaky integration along veering paths.

Authors:  Markus Lappe; Maren Stiels; Harald Frenz; Jack M Loomis
Journal:  Exp Brain Res       Date:  2011-05-01       Impact factor: 1.972

6.  Dynamics of mismatch correction in the hippocampal ensemble code for space: interaction between path integration and environmental cues.

Authors:  K M Gothard; W E Skaggs; B L McNaughton
Journal:  J Neurosci       Date:  1996-12-15       Impact factor: 6.167

7.  Spatial memory in the grey mouse lemur (Microcebus murinus).

Authors:  Mia-Lana Lührs; Melanie Dammhahn; Peter M Kappeler; Claudia Fichtel
Journal:  Anim Cogn       Date:  2009-03-05       Impact factor: 3.084

8.  Landmark navigation in a mantis shrimp.

Authors:  Rickesh N Patel; Thomas W Cronin
Journal:  Proc Biol Sci       Date:  2020-10-07       Impact factor: 5.349

9.  Selective hippocampal cholinergic deafferentation impairs self-movement cue use during a food hoarding task.

Authors:  Megan M Martin; Douglas G Wallace
Journal:  Behav Brain Res       Date:  2007-05-26       Impact factor: 3.332

10.  Translational motion perception and vestiboocular responses in the absence of non-inertial cues.

Authors:  S H Seidman
Journal:  Exp Brain Res       Date:  2007-08-07       Impact factor: 1.972

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