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15	
  

	
  

sometimes	
  present,	
  in	
  some	
  populations	
  of	
  wood	
  mice	
  (Fig.	
  1).	
  This	
  shows	
  shared	
  developmental	
  
potentialities	
  across	
  species	
  however	
  displaying	
  marked	
  differences	
  in	
  their	
  dental	
  pattern,	
  having	
  
diverged	
  more	
  than	
  10	
  million	
  years	
  ago.	
  	
  

Both	
  developmental	
  mechanisms	
  change	
  the	
  shape	
  of	
  the	
  tooth	
  without	
  perturbing	
  the	
  longitudinal	
  
alignment	
  of	
  the	
  cusps.	
  This	
  matches	
  a	
  strong	
  functional	
  requirement	
  during	
  occlusion	
  of	
  the	
  molars.	
  	
  
Murine	
  rodents	
  chew	
  along	
  a	
  longitudinal	
  (propalinal)	
  direction.	
  In	
  agreement,	
  the	
  arrangement	
  of	
  
the	
  cusps	
  evolved	
  into	
  longitudinal	
  rows	
  that	
  slide	
  into	
  gutters	
  in	
  the	
  occluding	
  molar	
  row	
  (Lazzari	
  et	
  
al.	
  2008).	
  Changes	
  related	
  to	
  Pmax,	
  being	
  the	
  concerted	
  spacing	
  of	
  all	
  cusps	
  or	
  a	
  local	
  anterior	
  
elongation,	
  occur	
  in	
  agreement	
  with	
  this	
  constraint.	
  Intra-­‐population	
  variants	
  along	
  Pmax,	
  and	
  
evolution	
  along	
  this	
  direction,	
  are	
  thus	
  prone	
  to	
  occur	
  because	
  such	
  mice,	
  at	
  any	
  step	
  of	
  their	
  
evolution,	
  display	
  functional	
  molar	
  rows	
  despite	
  variation	
  in	
  their	
  overall	
  shape.	
  	
  

	
  

Conclusion	
  

This	
  study	
  aimed	
  at	
  considering	
  evolutionary	
  patterns	
  in	
  wood	
  mouse	
  molar	
  shape	
  to	
  the	
  light	
  of	
  the	
  
intra-­‐population	
  variation	
  as	
  possible	
  ‘line	
  of	
  least	
  resistance	
  to	
  evolution’.	
  It	
  showed	
  the	
  potential	
  of	
  
this	
  approach	
  to	
  reconsider	
  striking	
  cases	
  of	
  parallel,	
  pronounced	
  and	
  fast	
  evolution,	
  mostly	
  on	
  
islands.	
  Considering	
  the	
  intra-­‐population	
  variance	
  as	
  a	
  hint	
  for	
  underlying	
  genetic/developmental	
  
networks,	
  this	
  means	
  that	
  evolution	
  on	
  islands	
  can	
  produce	
  fast	
  response	
  to	
  selection	
  and/or	
  drift	
  by	
  
modulating	
  existing	
  networks.	
  In	
  contrast,	
  only	
  reduced	
  differentiation	
  accumulated	
  between	
  
ancient	
  mainland	
  phylogenetic	
  lineages,	
  and	
  the	
  shape	
  changes	
  involved	
  were	
  independent	
  of	
  the	
  
direction	
  of	
  main	
  intra-­‐population	
  variance.	
  Evolution	
  among	
  the	
  continental	
  lineages	
  was	
  probably	
  
constrained	
  by	
  stabilizing	
  selection	
  in	
  this	
  generalist	
  species,	
  and	
  possibly	
  involved	
  small	
  genetic	
  
changes	
  not	
  related	
  to	
  the	
  networks	
  producing	
  the	
  main	
  variation,	
  accumulating	
  together	
  with	
  
genetic	
  divergence.	
  The	
  questions	
  opened	
  by	
  such	
  approaches	
  challenge	
  further	
  studies,	
  integrating	
  
evolutionary,	
  ecological,	
  functional	
  and	
  developmental	
  investigations,	
  that	
  are	
  needed	
  to	
  develop	
  a	
  
comprehensive	
  interpretation	
  of	
  the	
  processes	
  underlying	
  morphological	
  diversification	
  in	
  an	
  ‘eco-­‐
evo-­‐devo’	
  perspective.	
  

	
  

Acknowledgements	
  	
  
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