High-throughput simulations indicate feasibility of navigation by familiarity with a local sensor such as scorpion pectines

Scorpions have arguably the most elaborate “tongues” on the planet: two paired ventral combs, called pectines, that are covered in thousands of chemo-tactile peg sensilla and that sweep the ground as the animal walks. Males use their pectines to detect female pheromones during the mating season, but females have pectines too: What additional purpose must the pectines serve? Why are there so many pegs? We take a computational approach to test the hypothesis that scorpions use their pectines to navigate by chemo-textural familiarity in a manner analogous to the visual navigation-by-scene-familiarity hypothesis for hymenopteran insects. We have developed a general model of navigation by familiarity with a local sensor and have chosen a range of plausible parameters for it based on the existing behavioral, physiological, morphological, and neurological understanding of the pectines. Similarly, we constructed virtual environments based on the scorpion’s native sand habitat. Using a novel methodology of highly parallel high-throughput simulations, we comprehensively tested 2160 combinations of sensory and environmental properties in each of 24 different situations, giving a total of 51,840 trials. Our results show that navigation by familiarity with a local pectine-like sensor is feasible. Further, they suggest a subtle interplay between “complexity” and “continuity” in navigation by familiarity and give the surprising result that more complexity — more detail and more information — is not always better for navigational performance. Author summary Scorpions’ pectines are intricate taste-and-touch sensory appendages that brush the ground as the animal walks. Pectines are involved in detecting pheromones, but their exquisite complexity — a pair of pectines can have around 100,000 sensory neurons — suggests that they do more. One hypothesis is “Navigation by Scene Familiarity,” which explains how bees and ants use their compound eyes to navigate home: the insect visually scans side to side as it moves, compares what it sees to scenes learned along a training path, and moves in the direction that looks most familiar. We propose that the scorpions’ pectines can be used to navigate similarly: instead of looking around, they sweep side to side sensing local chemical and textural information. We crafted simulated scorpions based on current understanding of the pectines and tested their navigational performance in virtual versions of the animals’ sandy habitat. Using a supercomputer, we varied nine environmental, sensory, and situational properties and ran a total of 51,840 trials of simulated navigation. We showed that navigation by familiarity with a local sensor like the pectines is feasible. Surprisingly, we also found that having a more detailed landscape and/or a more sensitive sensor is not always optimal.

[1]  C. Hoffmann Zur Funktion der kammförmigen Organe von Skorpionen , 2004, Naturwissenschaften.

[2]  D. Gaffin,et al.  Investigating sensory processing in the pectines of the striped bark scorpion, Centruroides vittatus , 2019, Invertebrate Neuroscience.

[3]  John M. Melville,et al.  The pectines of scorpions : analysis of structure and function , 2000 .

[4]  Fei Peng,et al.  Using an Insect Mushroom Body Circuit to Encode Route Memory in Complex Natural Environments , 2016, PLoS Comput. Biol..

[6]  Douglas D. Gaffin,et al.  Evidence of Chemical Signaling in the Sand Scorpion, Paruroctonus mesaensis (Scorpionida: Vaejovida) , 2010 .

[7]  Johannes D. Seelig,et al.  Feature detection and orientation tuning in the Drosophila central complex , 2013, Nature.

[8]  Thomas S. Collett,et al.  How does the insect central complex use mushroom body output for steering? , 2018, Current Biology.

[9]  Gerbrand Ceder,et al.  Screening for high-performance piezoelectrics using high-throughput density functional theory , 2011 .

[10]  M. Srinivasan,et al.  Searching behaviour of desert ants, genusCataglyphis (Formicidae, Hymenoptera) , 2004, Journal of comparative physiology.

[11]  S. McIver,et al.  Structure of cuticular mechanoreceptors of arthropods. , 1975, Annual review of entomology.

[12]  H. Wolf The pectine organs of the scorpion, Vaejovis spinigerus: structure and (glomerular) central projections. , 2008, Arthropod structure & development.

[13]  Andrew Philippides,et al.  A Model of Ant Route Navigation Driven by Scene Familiarity , 2012, PLoS Comput. Biol..

[14]  Martin Egelhaaf,et al.  The fine structure of honeybee head and body yaw movements in a homing task , 2010, Proceedings of the Royal Society B: Biological Sciences.

[15]  Johannes D. Seelig,et al.  Neural dynamics for landmark orientation and angular path integration , 2015, Nature.

[16]  R. Wehner,et al.  Visual navigation in insects: coupling of egocentric and geocentric information , 1996, The Journal of experimental biology.

[17]  R. Wehner,et al.  Ant Navigation: One-Way Routes Rather Than Maps , 2006, Current Biology.

[18]  Douglas D. Gaffin Electrophysiological analysis of synaptic interactions within peg sensilla of scorpion pectines , 2002, Microscopy research and technique.

[19]  Guido C. H. E. de Croon,et al.  Visual Homing for Micro Aerial Vehicles Using Scene Familiarity , 2018, Unmanned Syst..

[20]  H. Wolf,et al.  Serotonin-immunoreactive neurons in scorpion pectine neuropils: similarities to insect and crustacean primary olfactory centres? , 2012, Zoology.

[21]  P. Graham,et al.  Ants use the panoramic skyline as a visual cue during navigation , 2009, Current Biology.

[22]  Andrew Philippides,et al.  Holistic visual encoding of ant-like routes: Navigation without waypoints , 2011, Adapt. Behav..

[23]  Michael Mangan,et al.  Insect navigation: do ants live in the now? , 2015, The Journal of Experimental Biology.

[24]  D. Gaffin,et al.  Functionally redundant peg sensilla on the scorpion pecten , 2011, Journal of Comparative Physiology A.

[25]  Andrew Philippides,et al.  Navigation-specific neural coding in the visual system of Drosophila , 2015, Biosyst..

[26]  D. Gaffin,et al.  A new tip-recording method to test scorpion pecten chemoresponses to water-soluble stimulants , 2010, Journal of Neuroscience Methods.

[27]  F. Barth,et al.  Arthropod touch reception: spider hair sensilla as rapid touch detectors , 2001, Journal of Comparative Physiology A.

[28]  A. Philippides,et al.  Vision for navigation: What can we learn from ants? , 2017, Arthropod structure & development.

[29]  David Mohrig,et al.  Methodology for reconstructing wind direction, wind speed and duration of wind events from aeolian cross‐strata , 2012 .

[30]  P. Brownell,et al.  Evidence of Mate Trailing in the Giant Hairy Desert Scorpion, Hadrurus arizonensis (Scorpionida, Iuridae) , 2004, Journal of Insect Behavior.

[31]  Gaby Maimon,et al.  A neural circuit architecture for angular integration in Drosophila , 2017, Nature.

[32]  Michael B. Reiser,et al.  Visual Place Learning in Drosophila melanogaster , 2011, Nature.

[33]  B. Webb,et al.  Neural mechanisms of insect navigation. , 2016, Current opinion in insect science.

[34]  Tim Landgraf,et al.  A neural network model for familiarity and context learning during honeybee foraging flights , 2017, Biological Cybernetics.

[35]  P. Brownell Glomerular Cytoarchitectures in Chemosensory Systems of Arachnids a , 1998, Annals of the New York Academy of Sciences.

[36]  S. Al-Moghrabi,et al.  Inorganic carbon uptake for photosynthesis by the symbiotic coral-dinoflagellate association II. Mechanisms for bicarbonate uptake , 1996 .

[37]  D. Krapp Contact Chemoreception of Prey in Hunting Scorpions (Arachnida: Scorpiones) , 2009 .

[38]  Rüdiger Wehner,et al.  Idiosyncratic route-based memories in desert ants, Melophorus bagoti: How do they interact with path-integration vectors? , 2005, Neurobiology of Learning and Memory.

[39]  Douglas D. Gaffin,et al.  Are They the Same, or Are They Different? , 2019, Euler's Gem.

[40]  Joaquin Ortega-Escobar,et al.  Role of the different eyes in the visual odometry in the wolf spider Lycosa tarantula (Araneae, Lycosidae) , 2017, Journal of Experimental Biology.

[41]  Douglas D Gaffin,et al.  Autonomous Visual Navigation of an Indoor Environment Using a Parsimonious, Insect Inspired Familiarity Algorithm , 2016, PloS one.

[42]  J. Ortega-Escobar ROLE OF THE ANTERIOR LATERAL EYES OF THE WOLF SPIDER LYCOSA TARENTULA (ARANEAE, LYCOSIDAE) DURING PATH INTEGRATION , 2006 .

[43]  Douglas D. Gaffin,et al.  Response properties of chemosensory peg sensilla on the pectines of scorpions , 1997, Journal of Comparative Physiology A.

[44]  Paul Graham,et al.  Image-matching during ant navigation occurs through saccade-like body turns controlled by learned visual features , 2010, Proceedings of the National Academy of Sciences.

[45]  Andrew Philippides,et al.  How might ants use panoramic views for route navigation? , 2011, Journal of Experimental Biology.

[46]  H. Wolf Scorpions pectines - Idiosyncratic chemo- and mechanosensory organs. , 2017, Arthropod structure & development.

[47]  N. Strausfeld,et al.  Mushroom bodies of the cockroach: Their participation in place memory , 1998, The Journal of comparative neurology.

[48]  D. Gaffin,et al.  Comparison of scorpion behavioral responses to UV under sunset and nighttime irradiances , 2014 .

[49]  Douglas D. Gaffin,et al.  Electrophysiological evidence of synaptic interactions within chemosensory sensilla of scorpion pectines , 1997, Journal of Comparative Physiology A.

[50]  N. Marzari,et al.  High-throughput computational screening for solid-state Li-ion conductors , 2019, Energy & Environmental Science.

[51]  W. D. Sissom,et al.  Scorpions of the Genus Paruroctonus from New Mexico and Texas (Scorpiones, Vaejovidae) , 1981 .

[52]  Paul Graham,et al.  Ant navigation: Priming of visual route memories , 2005, Nature.

[53]  Eleanor H. Slifer,et al.  The Structure of Arthropod Chemoreceptors , 1970 .

[54]  Matthew S. Taylor,et al.  Behavioral evidence of pheromonal signaling in desert grassland scorpions Paruroctonus utahensis , 2012 .

[55]  Stanley Heinze,et al.  Unraveling the neural basis of insect navigation. , 2017, Current opinion in insect science.

[56]  Antoine Wystrach,et al.  Landmarks or panoramas: what do navigating ants attend to for guidance? , 2011, Frontiers in Zoology.

[57]  U. Homberg,et al.  Organization and functional roles of the central complex in the insect brain. , 2014, Annual review of entomology.

[58]  Friedrich G. Barth,et al.  Compound slit sense organs on the spider leg: Mechanoreceptors involved in kinesthetic orientation , 1972, Journal of comparative physiology.

[59]  Barbara Webb,et al.  The internal maps of insects , 2019, Journal of Experimental Biology.

[60]  Ken Cheng,et al.  Searching behavior in social Hymenoptera , 2015 .

[61]  Alex D. M. Dewar,et al.  Insect-Inspired Navigation Algorithm for an Aerial Agent Using Satellite Imagery , 2015, PloS one.

[62]  R. Wehner,et al.  Multiroute memories in desert ants , 2008, Proceedings of the National Academy of Sciences.