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Whisker touch guides canopy exploration in a nocturnal, arboreal rodent, the Hazel dormouse (Muscardinus avellanarius)

Abstract

Dormouse numbers are declining in the UK due to habitat loss and fragmentation. We know that dormice are nocturnal, arboreal, and avoid crossing open spaces between habitats, yet how they navigate around their canopy is unknown. As other rodents use whisker touch sensing to navigate and explore their environment, this study investigates whether Hazel dormice (Muscardinus avellanarius) employ their whiskers to cross between habitats. We analysed high-speed video footage of dormice exploring freely in flat and climbing arenas in near darkness and using infrared light illumination. We confirm that, like rats and mice, dormice move their whiskers back and forth continuously (~10 Hz) in a motion called whisking and recruit them to explore small gaps (<10 cm) by increasing the amplitude and frequency of whisking and also the asymmetry of movement between the left and right whisker fields. When gaps between platforms are larger than 10–15 cm, dormice spend more time travelling on the floor. These findings suggest that dormice can actively and purposively move their whiskers to gather relevant information from their canopy at night. As this species is vulnerable to threats on the ground, we also provide evidence that joining habitat patches between dormouse populations is important for promoting natural behaviours and movement between patches.

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Abbreviations

RC:

Rostrocaudal

DC:

Dorsoventral

BWTT:

BIOTACT Whisker Tracking Tool

References

  • Ahl AS (1986) The role of vibrissae in behavior: a status review. Vet Res Commun 10(1):245–268

    Article  CAS  PubMed  Google Scholar 

  • Arkley K, Grant RA, Mitchinson B, Prescott TJ (2014) Strategy change in vibrissal active sensing during rat locomotion. Curr Biol 24(13):1507–1512

    Article  CAS  PubMed  Google Scholar 

  • Berg L, Berg à (1999) Abundance and survival of the hazel dormouse Muscardinus avellanarius in a temporary shrub habitat: a trapping study. In Annales Zoologici Fennici 36(3):159–165

    Google Scholar 

  • Bhattacharyya U, Bhalla US (2015) Robust and rapid air borne odor tracking without casting. eNeuro. doi:10.1523/ENEURO.0102-15.2015

    PubMed  PubMed Central  Google Scholar 

  • Bright PW (1998) Behaviour of specialist species in habitat corridors: arboreal dormice avoid corridor gaps. Anim Behav 56(6):1485–1490

    Article  CAS  PubMed  Google Scholar 

  • Bright PW, Morris PA (1991) Ranging and nesting behaviour of the dormouse, Muscardinus avellanarius, in diverse low-growing woodland. J Zool (Lond) 224:177–190

    Article  Google Scholar 

  • Bright PW, Morris PA (1992) Ranging and nesting behaviour of the dormouse, Muscardinus avellanarius, in coppice-with-standard woodland. J Zool (Lond) 226:589–600

    Article  Google Scholar 

  • Bright PW, Morris PA (1996) Why are dormice rare? A case study in conservation biology. Mamm Rev 26(4):157–187

    Article  Google Scholar 

  • Bright PW, Mitchel P, Morris PA (1994) Dormouse distribution: survey techniques, insular ecology and selection of sites for conservation. J Appl Ecol 31:329–339

    Article  Google Scholar 

  • Bright P, Morris P, Mitchell-Jones T (2006) The dormouse conservation handbook. English Nature, the Rural Development Service and the Countryside Agency

  • Brown D, Wolfgang C (2015) Tracker 4.8 xs. Cabrillo College. http://www.cabrillo.edu/~dbrown/tracker/. Accessed 8th September 2015

  • Büchner S (2008) Dispersal of common dormice Muscardinus avellanarius in a habitat mosaic. Acta Theriol 53:259–262

    Article  Google Scholar 

  • Cote J, Clobert J, Brodin T, Fogarty S, Sih A (2010) Personality-dependent dispersal: characterization, ontogeny and consequences for spatially structured populations. Philos T Roy Soc B 365(1560):4065–4076

    Article  CAS  Google Scholar 

  • Goodale MA, Ellard CG, Booth L (1990) The role of image size and retinal motion in the computation of absolute distance by the Mongolian gerbil (Meriones unguiculatus). Vision Res 30(3):399–413

    Article  CAS  PubMed  Google Scholar 

  • Grant RA, Arkley K (2015) Matched filtering in active whisker touch. In: von Der Emde G, Warrant E (eds) The ecology of animal senses. Springer, pp 59–82

  • Grant RA, Mitchinson B, Fox CW, Prescott TJ (2009) Active touch sensing in the rat: anticipatory and regulatory control of whisker movements during surface exploration. J Neurophysiol 101(2):862–874

    Article  PubMed  Google Scholar 

  • Grant RA, Haidarliu S, Kennerley NJ, Prescott TJ (2013) The evolution of active vibrissal sensing in mammals: evidence from vibrissal musculature and function in the marsupial opossum Monodelphis domestica. J Exp Biol 216(18):3483–3494

    Article  PubMed  Google Scholar 

  • Grant RA, Delaunay MG, Haidarliu S (2016). Mystacial whisker layout and musculature in the guinea pig (Cavia porcellus): a social, diurnal mammal. Anat Rec (Hoboken). doi:10.1002/ar.23504

    Google Scholar 

  • Grzimek B, Schlager N, Olendorf D, McDade MC (2003) Grzimek’s animal life encyclopedia, 2nd edn. Gale

  • Haidarliu S, Simony E, Golomb D, Ahissar E (2010) Muscle architecture in the mystacial pad of the rat. Anat Rec (Hoboken) 293(7):1192–1206

    Article  Google Scholar 

  • Haidarliu, S, Kleinfeld D, Deschênes M, Ahissar E (2015) The musculature that drives active touch by vibrissae and nose in mice. Anat Rec (Hoboken) 298(7):1347–1358

    Article  Google Scholar 

  • Hewitt B, Hoon Yap M, Grant RA (2016) Manual whisker annotator (MWA): a modular open source tool. J Open Res Soft 4:e16. doi:10.5334/jors.93

    Article  Google Scholar 

  • Jenkinson EW, Glickstein M (2000) Whiskers, barrels, and cortical efferent pathways in gap crossing by rats. J Neurophysiol 84(4):1781–1789

    CAS  PubMed  Google Scholar 

  • Kahmann H, Ostermann K (1951) Wahrnehmen und hervorbringen hoher töne bei kleinen Säugetieren. Cell Mol Life Sci 7(7):268–269

    Article  CAS  Google Scholar 

  • Knutsen PM, Ahissar E (2008) Orthogonal coding of object location. Trends Neurosci 32(3):101–109

    PubMed  Google Scholar 

  • Legg CR, Lambert S (1990) Distance estimation in the hooded rat: experimental evidence for the role of motion cues. Behav Brain Res 41(1):11–20

    Article  CAS  PubMed  Google Scholar 

  • Mitchinson B, Grant RA, Arkley K, Rankov V, Perkon I, Prescott TJ (2011) Active vibrissal sensing in rodents and marsupials. Philos T Roy Soc B 366(1581):3037–3048

    Article  Google Scholar 

  • Morris PA (2003) A review of research on British dormice (Gliridae) and the effect of increasing public and scientific awareness of these animals. Acta Zool Hung 49(Suppl 1):125–130

    Google Scholar 

  • Mortelitti A, Santarelli L, Sozio G, Fagiani S, Boitani L (2013) Long distance field crossings by hazel dormice (Muscardinus avellanarius) in fragmented landscapes. Mamm Biol 78:309–312

    Google Scholar 

  • Mortelliti A, Amori G, Capizzi D, Cervone C, Fagiani S, Pollini B, Boitani L (2011) Independent effects of habitat loss, habitat fragmentation and structural connectivity on the distribution of two arboreal rodents. J Appl Ecol 48(1):153–162

    Article  Google Scholar 

  • Niederschuh SJ, Witte H, Schmidt, M (2015) The role of vibrissal sensing in forelimb position control during travelling locomotion in the rat (Rattus norvegicus, Rodentia). Zool 118(1):51–62

    Article  Google Scholar 

  • Perkon I, Košir A, Itskov PM, Tasič J, Diamond ME (2011) Unsupervised quantification of whisking and head movement in freely moving rodents. J Neurophysiol 105(4):1950–1962

    Article  PubMed  Google Scholar 

  • Pocock RI (1914) On the facial vibrissae of Mammalia. Zoology 84(4):889–912

    Google Scholar 

  • Prescott TJ, Diamond ME, Wing AM (2011) Active touch sensing. Philos T Roy Soc B 366(1581):2989–2995

    Article  Google Scholar 

  • Ramakers JJ, Dorenbosch M, Foppen RP (2014) Surviving on the edge: a conservation-oriented habitat analysis and forest edge manipulation for the hazel dormouse in the Netherlands. Eur J Wildl Res 60(6):927–931

    Article  Google Scholar 

  • Raynaud J, Schradin C (2014) Experimental increase of testosterone increases boldness and decreases anxiety in male African striped mouse helpers. Physiol Behav 129:57–63

    Article  CAS  PubMed  Google Scholar 

  • Schmidt A, Fischer MS (2010) Arboreal locomotion in rats: the challenge of maintaining stability. J Exp Biol 213:3615–3624

    Article  PubMed  Google Scholar 

  • Schroeder JB, Ritt JT (2016) Selection of head and whisker coordination strategies during goal oriented active touch. J Neurophysiol 115:1797–1809

    Article  PubMed  Google Scholar 

  • Stride I (2009) Dormouse bridge design and use. Unpublished report to the People’s Trust for Endangered Species. http://www.ptes.org/files/1262_dormice_bridges_final_report_1.pdf. Viewed May 2015

  • Thomas JA, Moss CF, Vater M (2004) Echolocation in bats and dolphins. University of Chicago Press

  • Vincent SB (1912) The function of the vibrissae of the white rat. Behav Monogr 1:1–86

    Google Scholar 

  • Wallace DJ, Greenberg DS, Sawinski J, Rulla S, Notaro G, Kerr JN (2013) Rats maintain an overhead binocular field at the expense of constant fusion. Nature 498(7452):65–69

    Article  CAS  PubMed  Google Scholar 

  • Watson JB (1907) Kinaesthetic and organic sensations: their role in the reactions of the white rat to the maze. Psychol Rev Monogr Suppl 8:1–100

    Google Scholar 

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Acknowledgements

The authors would like to thank Hazel Ryan for her continued help and support, especially in handling the dormice; also to Hazel Ryan and Angus Carpenter for their comments on the manuscript. We are extremely thankful to the Wildwood Trust for the use of their facilities and animals. The authors are also grateful to Ben Mitchinson for designing the climbing arenas and developing the portable setup, and to Holly Langridge and Fraser Combe for data collection support. Thanks to Brendan O’Connor for finding and translating some of the literature. Video analysis was performed using the BIOTACT Whisker Tracking Tool which was created under the auspices of the FET Proactive project FP7 BIOTACT project (ICT 215910), which also partly funded the study, alongside a small project grant from the British Ecological Society (BES). A big thanks goes to the CEB Research Group at MMU for listening to results summaries and advising about the project direction.

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Correspondence to Robyn A. Grant.

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All animals were part of a rescue and rehabilitation program, or from a breeding pool at the Wildwood Trust in Kent (UK) and approved by local ethics committees at each of the academic institutions and at the Wildwood Trust.

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Arkley, K., Tiktak, G.P., Breakell, V. et al. Whisker touch guides canopy exploration in a nocturnal, arboreal rodent, the Hazel dormouse (Muscardinus avellanarius). J Comp Physiol A 203, 133–142 (2017). https://doi.org/10.1007/s00359-017-1146-z

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  • DOI: https://doi.org/10.1007/s00359-017-1146-z

Keywords

  • Whisker
  • Vibrissa
  • Active touch sensing
  • Dormouse
  • Climbing