Abstract
The aim of blended cognition is to contribute to the design of more realistic and efficient robots by looking at the way humans can combine several kinds of affective, cognitive, sensorimotor and perceptual representations. This chapter is about vision-for-action. In humans and non-human primates (as well as in most of mammals), motor behavior in general and visuomotor representations for grasping in particular are influenced by emotions and affective perception of the salient properties of the environment. This aspect of motor interaction is not examined in depth in the biologically plausible robot models of grasping that are currently available. The aim of this chapter is to propose a model that can help us to make neurorobotics solutions more embodied, by integrating empirical evidence from affective neuroscience with neural evidence from vision and motor neuroscience. Our integration constitutes an attempt to make a neurorobotic model of vision and grasping more compatible with the insights proposed by the embodied view of cognition and perception followed in neuroscience, which seems to be the only one able to take into account the biological complexity of cognitive systems and, accordingly, to duly explain the high flexibility and adaptability of cognitive systems with respect to the environment they inhabit.
“What I cannot build,
I cannot understand”.
Richard Feynman
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Notes
- 1.
Precisely, the dorso-dorsal stream (D-D), also known as the dorso-medial circuit, projects to the dorsal premotor cortex and, following the division of the intraparietal sulcus that subdivides the posterior parietal lobe, is related to the superior parietal lobule (SPL); the ventro-dorsal stream (V-D), also known as the dorso-lateral circuit, projects to the ventral premotor cortex and is related to the inferior parietal lobule (IPL) (see Rozzi et al. 2006; Chinellato et al. 2011; Gallese 2007; Turella and Lignau 2014; Rizzolatti and Matelli 2003; Jeannerod and Jacob 2005; Kravitz et al. 2011; Binkofski and Buxbaum 2013; Hoeren et al. 2013; see also Glover 2004).
- 2.
- 3.
All this is in line with the idea that the OFC is crucial in changing behavior in the face of unexpected outcomes (Schoenbaum et al. 2009).
References
Aglioti S, DeSouza JFX, Goodale MA (1995) Size-contrast illusions deceive the eye but not the hand. Curr Biol 5:679–685
Algom D, Chajut E, Lev S (2004) A rational look at the emotional stroop phenomenon: a generic slowdown, not a stroop effect. J Exp Psychol Gen 133:323–338. 10.1037/0096-3445.133.3.323
Alsmith AJT, de Vignemont F (2012) Embodying the mind and representing the body. Rev Phil Psych 3:1–13. https://doi.org/10.1007/s13164-012-0085-4
Anelli F, Borghi AM, Nicoletti R (2012) Grasping the pain: motor resonance with dangerous affordances. Conscious Cogn 21:1627–1639
Anelli F, Nicoletti R, Bolzani R, Borghi AM (2013a) Keep away from danger: dangerous objects in dynamic and static situations. Front Hum Neurosci 7:344. https://doi.org/10.3389/fnhum.2013.00344
Anelli F, Ranzini M, Nicoletti R, Borghi AM (2013b) Perceiving object dangerousness: an escape from pain? Exp Brain Res 228:457–466. https://doi.org/10.1007/s00221-013-3577-2
Ansuini C, Santello M, Massaccesi S, Castiello U (2006) Effects of end-goal on hand shaping. J Neurophysiol 95(4):2456–2465. https://doi.org/10.1152/jn.01107.2005
Aron AR, Verbruggen F (2008) Stop the presses: dissociating a selective from a global mechanism for stopping. Psychol Sci 19:1146–1153
Barrett LF, Bar LF (2009) See it with feeling: affective predictions during object perception. Philos Trans R Soc 364:1325–1334. https://doi.org/10.1098/rstb.2008.0312
Baumann MA, Fluet M-C, Scherberger H (2009) Context-specific grasp movement representation in the macaque anterior intraparietal area. J Neurosci 29:6436–6448
Bicchi A (2000) Hand for dexterous manipulation and robust grasping: a difficult road towards simplicity. IEEE Trans Robot Autom 16(6):652–662
Binkofski F, Buxbaum LJ (2013) Two action systems in the human brain. Brain Lang 127(2):222–229. https://doi.org/10.1016/j.bandl.2012.07.007
Borghi AM, Riggio L (2015) Stable and variable affordances are both automatic and flexible. Front Hum Neurosci 9:351. https://doi.org/10.3389/fnhum.2015.00351
Borghi AM, Gianelli C, Scorolli C (2010) Sentence comprehension: effectors and goals, self and others. An overview of experiments and implications for robotics. Front Neurorobot 4(3). https://doi.org/10.3389/fnbot.2010.00003
Borra E, Belmalih A, Calzavara R, Gerbella M, Murata A, Rozzi S, Luppino G (2008) Cortical connections of the macaque anterior intraparietal (AIP) area. Cereb Cortex 18:1094–1111
Briscoe R (2009) Egocentric spatial representation in action and perception. Philos Phenomenol Res 79:423–460
Briscoe R, Schwenkler J (2015) Conscious vision in action. Cogn Sci 39(7):1435–1467
Brogaard B (2011) Conscious vision for action versus unconscious vision for action? Cogn Sci 35:1076–1104
Bruno N, Battaglini PP (2008) Integrating perception and action through cognitive neuropsychology (broadly conceived). Cogn Neuropshycol 25(7–8):879–890
Buccino G, Sato M, Cattaneo L, Rodà F, Riggio L (2009) Broken affordances, broken objects: a TMS study. Neuropsychologia 47:3074–3078. https://doi.org/10.1016/j.neuropsychologia.2009.07.003
Budisavljevic S, Dell’Acqua F, Zanatto D, Begliomini C, Miotto D, Motta R, Castiello U (2016) Asymmetry and structure of the fronto-parietal networks underlie visuomotor processing in humans. Cereb Cortex. https://doi.org/10.1093/cercor/bhv348
Bullier J, Hupé JM, James AC, Girard P (2001) The role of feedback connections in shaping the responses of visual cortical neurons. Prog Brain Res 134:193–204
Cai W, Oldenkamp CL, Aron AR (2011) A proactive mechanism for selective suppression of response tendencies. J Neurosci 31:5965–5969
Caligiore D, Borghi AM, Parisi D, Baldassarre G (2010) TRoPICALS: a computational embodied neuroscience model of experiments on compatibility effects. Psychol Rev 117:1188–1228. https://doi.org/10.1037/a0020887
Caligiore D, Borghi AM, Parisi D, Ellis R, Cangelosi A, Baldassarre G (2013) How affordances associated with a distractor object affect compatibility effects: a study with the computational model TRoPICALS. Psychol Res 77(1):7–19
Caligiore D, Borghi AM, Parisi D, Ellis R, Cangelosi A, Baldassarre G (eds) (2013b) How affordances associated with a distractor object affect compatibility effects: a study with the computational model TRoPICALS. Psychol Res 77:7–19. https://doi.org/10.1007/s00426-012-0424-1
Castiello U (2005) The neuroscience of grasping. Nat Rev 6(9):726–736. https://doi.org/10.1038/nrn1744
Castiello U, Begliomini C (2008) The cortical control of visually guided grasping. Neuroscientist 14(2):157–170. https://doi.org/10.1177/1073858407312080 (Epub 2008 Jan 24)
Cavada C, Company T, Tejedor J, Cruz-Rizzolo RJ, Reinsos-Suarez F (2000) The anatomical connections of the macaque monkey orbitofrontal cortex: a review. Cereb Cortex 10:220–242. https://doi.org/10.1093/cercor/10.3.220
Chemero A (2009) Radical embodied cognitive science. The MIT Press, Cambridge, MA
Chinellato E, del Pobil AP (2008) fRI, functional robotic imaging: Visualizing a robot brain. In: IEEE international conference on distributed human-machine systems
Chinellato E, del Pobil AP (2016) The visual neuroscience of robotic grasping. Achieving sensorimotor skills through dorsal-ventral stream integration. Springer International Publishing, Cham
Chinellato E, Grzyb BJ, Marzocchi N, Bosco A, Fattori P, del Pobil AP (2011) The Dorso-medial visual stream: from neural activation to sensorimotor interaction. Neurocomputing 74:1203–1212
Cisek P (2007) Cortical mechanisms of action selection: the affordance competition hypothesis. Philos Trans R Soc Biol Sci 362:1585–1599. https://doi.org/10.1098/rstb.2007.2054
Cisek P, Kalaska JF (2010) Neural mechanisms for interacting with a world full of action choices. Annu Rev Neurosci 33:269–298
Claffey MP, Sheldon S, Stinear CM, Verbruggen F, Aron AR (2010) Having a goal to stop action is associated with advance control of specific motor representations. Neuropsychologia 48(2):541–548. https://doi.org/10.1016/j.neuropsychologia.2009.10.015 Epub 2009 Oct 29
Cohen NR, Cross ES, Tunik E, Grafton ST, Culham JC (2009) Ventral and dorsal stream contributions to the online control of immediate and delayed grasping: a TMS approach. Neuropsychologia 47(6):1553–1562. https://doi.org/10.1016/j.neuropsychologia.2008.12.034
Colombetti G (2007) Enactive appraisal. Phenomenol Cogn Sci 6:527–546
Colombetti G (2013) The feeling body: affective science meets the enactive mind. The MIT Press, Cambridge, MA
Colombetti G, Thompson E (2008) The feeling body: toward an enactive approach to emotion. In: Overton WF, Müller U, Newman J (eds) Developmental perspectives on embodiment and consciousness. Lawrence Erlbaum, New York, pp 45–68
Costantini M, Ambrosini E, Tieri G, Sinigaglia C, Committeri G (2010) Where does an object trigger an action? An investigation about affordances in space. Exp Brain Res 207:95–103. https://doi.org/10.1007/s00221-010-2435-8
Creem SH, Proffitt DR (2001) Grasping objects by their handles: a necessary interaction between cognition and action. J Exp Psychol Hum Percept Perform 27(1):218–228
Culham JC (2006) Functional neuroimaging: experimental design and analysis. In: Cabeza R, Kingstone A (eds) Handbook of functional neuroimaging of cognition. MIT Press, Cambridge, pp 53–82
Culham JC, Cavina-Pratesi C, Singhal A (2006) The role of parietal cortex in visuomotor control: what have we learned from neuroimaging? Neuropsychologia 44(13):2668–2684. https://doi.org/10.1016/j.neuropsychologia.2005.11.003
Delafield-Butt JT, Gangopadhyay N (2013) Sensorimotor intentionality: the origins of intentionality in prospective agent action. Dev Rev 33:399–425
Derbyshire N, Ellis R, Tucker M (2006) The potentiation of two components of the reach-to-grasp action during object categorisation in visual memory. Acta Psychol 122(1):74–98
Dijkerman HC, McIntosh RD, Schindler I, Nijboer TCW, Milner AD (2009) Choosing between alternative wrist postures: action planning needs perception. Neuropsychologia 47(6):1476–1482. https://doi.org/10.1016/j.neuropsychologia.2008.12.002
Duffy BR, Joue G (2000) Intelligent robots: the question of embodiment, BRAIN-MACHINE December 20-22, 2000, Ankara, Turkey effects: a study with the computational model TRoPICALS. Psychol Res 77(1):7–19. https://doi.org/10.1007/s00426-012-0424-1 Epub 2012 Feb 11
Eiben AE (2014) Grand challenges for evolutionary robotics. Front Robot AI, SPECIALTY GRAND CHALLENGE ARTICLE 1(4) https://doi.org/10.3389/frobt.2014.00004
Eiben AE, Kernbach S, Haasdijk E (2012) Embodied artificial evolution – artificial evolutionary systems in the 21st century. Evol Intell 5:261–272. https://doi.org/10.1007/s12065-012-0071-x
Eiben A, Bredeche N, Hoogendoorn M, Stradner J, Timmis J, Tyrrell A et al (2013) The triangle of life: evolving robots in real-time and real-space. In: Liò OM, Nicosia G, Nolfi S, Pavone M (eds) Advances in artificial life, ECAL 2013. MIT Press, Cambridge, MA, pp 1056–1063
Elliott R, Dolan RJ, Frith CD (2000) Dissociable functions in the medial and lateral orbitofrontal cortex: evidence from human neuroimaging studies. Cereb Cortex 10(3):308–317. https://doi.org/10.1093/cercor/10.3.308
Ellis R, Tucker M (2000) Micro-affordance: the potentiation of components of action by seen objects. Br J Psychol 91:451–471
Fadiga L, Fogassi L, Gallese V, Rizzolatti G (2000) Visuomotor neurons: ambiguity of the discharge or ‘motor’ perception? Int J Psychophysiol 35:165–177
Ferretti G (2016a) Neurophysiological states and perceptual representations: the case of action properties detected by the ventro-dorsal stream. In: Magnani L, Casadio C (eds) Model-based reasoning in science and technology. Models and inferences: logical, epistemological, and cognitive issues, Series “Sapere”, Studies in applied philosophy and rational ethics. Springer, Heidelberg
Ferretti G (2016b) Pictures, action properties and motor related effects. Synthese. https://doi.org/10.1007/s11229-016-1097-x
Ferretti G (2016c) Through the forest of motor representations. Conscious Cogn 43:177–196. https://doi.org/10.1016/j.concog.2016.05.013
Ferretti G (2016d) Visual feeling of presence. Pac Philos Q. https://doi.org/10.1111/papq.12170
Ferretti G (2017a) Pictures, emotions, and the dorsal/ventral account of picture perception. Rev Philos Psychol. https://doi.org/10.1007/s13164-017-0330-y
Ferretti G (2017b) Two visual systems in molyneux subjects. Phenomenol Cogn Sci 17(4):643–679. https://doi.org/10.1007/s11097-017-9533-z
Ferretti G (2017c) Are pictures peculiar objects of perception? J Am Philos Assoc 3(3):372–393. https://doi.org/10.1017/apa.2017.28
Ferretti G (forthcoming) The neural dynamics of seeing-in. Erkenntnis
Ferretti G, Alai M (2016) Enactivism, representations and canonical neurons. Argumentation 1:2
Ferretti, G, and Zipoli Caiani, S. (2018). Solving the Interface Problem without Translation: the Same Format Thesis. Pacific Philosophical Quarterly. https://doi.org/10.1111/papq.12243.
Floreano D, Husbands P, Nolfi S (2008) Evolutionary robotics. In: Siciliano B, Khatib O (eds) Springer handbook of robotics, vol G.61. Springer, Berlin, pp 1423–1451
Fogassi L, Luppino G (2005) Motor functions of the parietal lobe. Curr Opin Neurobiol 2005(15):626–631. https://doi.org/10.1016/j.conb.2005.10.015
Frank MJ, Loughry B, O’Reilly RC (2001) Interactions between frontal cortex and basal ganglia in working memory: a computational model. Cogn Affect Behav Neurosci 1:137–160
Gallagher S (2005) How the body shapes the mind. Oxford University Press, New York, 284 pp. ISBN:284, 0199271941
Gallese V (2007) The “conscious” dorsal stream: embodied simulation and its role in space and action conscious awareness. Psyche 13(1):1–20
Gallese V, Craighero L, Fadiga L, Fogassi L (1999) Perception through action. Psyche 5(21):1
Gibson JJ (1979) The ecological approach to visual perception. Houghton Mifflin, Boston
Glover S (2004) Separate visual representations in the planning and control of action. Behav Brain Sci 27:3–78
Goldman AI (2012) A moderate approach to embodied cognitive science. Rev Phil Psych 3:71–88. https://doi.org/10.1007/s13164-012-0089-0
Goldman AI (2012b) A moderate approach to embodied cognitive science. Rev Phil Psych 3:71–88. https://doi.org/10.1007/s13164-012-0089-0
Goodale MA, Milner AD (2004a) Sight unseen. Oxford University Press, Oxford
Goodale MA, Milner AD (2004b) Plans for action. Behav Brain Sci 27:37–40
Himmelbach M, Karnath HO (2005) Dorsal and ventral stream interaction: contributions from optic ataxia. J Cogn Neurosci 17(4):632–640. https://doi.org/10.1162/0898929053467514
Hoeren M, Kaller CP, Glauche V, Vry MS, Rijntjes M, Hamzei F, Weiller C (2013) Action semantics and movement characteristics engage distinct processing streams during the observation of tool use. Exp Brain Res 229(2):243–260. https://doi.org/10.1007/s00221-013-3610-5
Ikkai A, Jerde TA, Curtis CE (2011) Perception and action selection dissociate human ventral and dorsal cortex. J Cogn Neurosci 23(6):1494–1506. https://doi.org/10.1162/jocn.2010.21499
Jacob P, Jeannerod M (2003) Ways of seeing: the scope and limits of visual cognition. Oxford University Press, Oxford
Janssen P, Vogels R, Liu Y, Orban GA (2001) Macaque inferior temporal neurons are selective for three-dimensional boundaries and surfaces. J Neurosci 21:9419–9429
Jeannerod M, Jacob P (2005) Visual cognition: a new look at the two-visual systems model. Neuropsychologia 43:301–312
Kandel ERJH, Schwartz TM, Jessell SA, Siegelbaum A, Hudspeth J (2013) Principles of neural science. McGraw Hill Medical, New York
Kaplan E (2004) The M, P, and K pathways of the primate visual system. In: Chalupa LM, Werner JS (eds) The visual neuroscience. The MIT Press, Cambridge, MA, pp 481–494
Kitadono K, Humphreys GW (2009) Sustained interactions between perception and action in visual extinction and neglect: evidence from sequential pointing. Neuropsychologia 47(6):1592–1599. https://doi.org/10.1016/j.neuropsychologia.2008.11.010
Kondo H, Saleem KS, Price JL (2003) Differential connections of the temporal pole with the orbital and medial prefrontal networks in macaque monkeys. J Comp Neurol 465:499–523. https://doi.org/10.1002/cne.10842
Kragic D, Christensen HI (2003) Biologically motivated visual servoing and grasping for real world tasks. In: IEEE international conference on intelligent robots and systems, Las Vegas, USA
Kravitz DJ, Saleem KI, Baker CI, Mishkin M (2011) A new neural framework for visuospatial processing. Nat Rev Neurosci 12:217–230
Kravitz DJ, Saleem KS, Baker CI, Ungerleider LG, Mishkin M (2013) The ventral visual pathway: an expanded neural framework for the processing of object quality. Trends Cogn Sci 17(1):26–49
Kringelbach ML, Rolls ET (2004) The functional neuroanatomy of the human orbitofrontal cortex: evidence from neuroimaging and neuropsychology. Prog Neurobiol 72(5):341–372
Kveraga K, Boshyan J, Bar M (2007a) Magnocellular projections as the trigger of top-down facilitation in recognition. J Neurosci 27(48):13232–13240. https://doi.org/10.1523/JNEUROSCI.3481-07.2007
Kveraga K, Ghuman AS, Bar M (2007b) Top-down predictions in the cognitive brain. Brain Cogn 65:145–168. https://doi.org/10.1016/j.bandc.2007.06.007
Laschi C, Asuni G, Teti G, Carrozza M, Dario P, Guglielmelli E, Johansson R (2006) A bio- inspired neural sensory-motor coordination scheme for robot reaching and preshaping. In: IEEE international conference on biomedical robotics and biomechatronics, pp 531–536
Latash ML, Zatsiorsky VM (2009) Multi-finger prehension: control of a redundant mechanical system. Adv Exp Med Biol 629:597–618. https://doi.org/10.1007/978-0-387-77064-2_32
Laycock R, Crewther SG (2008) Towards an understanding of the role of the ‘magnocellular advantage’ in fluent reading. Neurosci Biobehav Rev 32:1494–1506. https://doi.org/10.1016/j.neubiorev.2008.06.002
Laycock R, Crewther SG, Crewther DP (2007) A role for the ‘magnocellular advantage’ in visual impairments in neurodevelopmental and psychiatric disorders. Neurosci Biobehav Rev 31:363–376. https://doi.org/10.1016/j.neubiorev.2006.10.003
Laycock R, Crewther DP, Fitzgerald PB, Crewther SG (2009) TMS disruption of V5/MT+ indicates a role for the dorsal stream in word recognition. Exp Brain Res 197:69–79. https://doi.org/10.1007/s00221-009-1894-2
Lebedev MA, Wise SP (2002) Insights into seeing and grasping: distinguishing the neural correlates of perception and action. Behav Cogn Neurosci Rev 1(2):108–129. https://doi.org/10.1177/1534582302001002002
Martin A (2007) The representation of object concepts in the brain. Annu Rev Psychol 58:25–45. https://doi.org/10.1146/annurev.psych.57.102904.190143
McIntosh RD, Schenk T (2009) Two visual streams for perception and action: current trends. Neuropsychologia 47(6):1391–1396. https://doi.org/10.1016/j.neuropsychologia.2009.02.009 (Epub 2009 Feb 13)
Milner A, Goodale M (1995/2006) The visual brain in action, 2nd edn. Oxford University Press, Oxford
Milner AD, Goodale MA (2008) Two visual systems re-viewed. Neuropsychologia 46:774–785
Morales A, Chinellato E, Fagg AH, del Pobil AP (2004) Using experience for assessing grasp reliability. Int J Humanoid Rob 1(4):671–691
Munakata Y, Herd SA, Chatham CH, Depue BE, Banich MT, O’Reilly RC (2011) A unified framework for inhibitory control. Trends Cogn Sci 15(10):453–459
Nakata H, Sakamoto K, Ferretti A, Gianni Perrucci M, Del Gratta C, Kakigi R, Luca RG (2008) Somato-motor inhibitory processing in humans: an event-related functional MRI study. NeuroImage 39(4):1858–1866
Nanay B (2011) Do we sense modalities with our sense modalities? Ratio 24:299–310
Nanay B (2013) Between perception and action. Oxford University Press, Oxford
Nanay B (2014) Empirical problems with anti-representationalism. In: Brogaard B (ed) Does perception have content? Oxford University Press, New York
Napier JR (1955) The form and function of the carpo-metacarpal joint of the thumb. J Anat 89:362–369
Napier JR (1956) The prehensile movements of the human hand. J Bone Joint Surg Br 38-B:902–913
Noë A (2004) Action in perception. The MIT Press, Cambridge, MA
Nolfi S, Floreano D (2000) Evolutionary robotics: the biology, intelligence, and technology of self-organizing machines. MIT Press, Cambridge, MA
O’Reilly RC (2010) The what and how of prefrontal cortical organization. Trends Neurosci 33(8):355–361. https://doi.org/10.1016/j.tins.2010.05.002
Pammer K, Hansen P, Holliday I, Cornelissen P (2006) Attentional shifting and the role of the dorsal pathway in visual word recognition. Neurophychology 44(14):2926–2936
Pfeifer R, Bongard J (2006) How the body shapes the way we think. MIT Press, Cambridge, MA
Pfeifer R, Lungarella M, Fumyia I (2007) Self-organization, embodiment, and biologically inspired robotics. Science 318(5853):1088–1093. https://doi.org/10.1126/science.1145803
Price JL (2007) Connections of orbital cortex. In: Zald DH, Rauch SL (eds) The orbitofrontal cortex. Oxford University Press, New York, pp 38–56
Raos V, Umiltà MA, Murata A, Fogassi L, Gallese V (2006) Functional properties of grasping-related neurons in the ventral premotor area F5 of the macaque monkey. J Neurophysiol 95:709–729
Riggio L, Patteri I, Oppo A, Buccino G, Umiltà C (2006) The role of affordances in inhibition of return. Psychon Bull Rev 13:1085–1090. https://doi.org/10.3758/bf03213930
Rizzolatti G, Matelli M (2003) Two different streams form the dorsal visual system: anatomy and functions. Exp Brain Res 153:146–157
Rizzolatti G, Sinigaglia C (2008) Mirrors in the brain how our minds share actions and emotions. Oxford University Press, Oxford
Romero MC, Pani P, Janssen P (2014) Coding of shape features in the macaque anterior intraparietal area systems/circuits 4006. J Neurosci 34(11):4006–4021
Rozzi S, Calzavara R, Belmalih A, Borra E, Gregoriou GG, Matelli M, Luppino G (2006) Cortical connections of the inferior parietal cortical convexity of the macaque monkey. Cereb Cortex 16(10):1389–1417. https://doi.org/10.1093/cercor/bhj076
Saxena A, Driemeyer J, Ng AY (2008) Robotic grasping of novel objects using vision. Int J Robot Res 27(2):157–173. https://doi.org/10.1177/0278364907087172
Schenk T, McIntosh RD (2010) Do we have independent visual streams for perception and action? Cogn Neurosci 1:52–78
Schieber MH, Santello M (2004) Hand function: peripheral and central constraints on performance. J Appl Physiol 96(6):2293–2300
Schindler I, Rice NJ, McIntosh RD, Rossetti Y, Vighetto A, Milner AD (2004) Automatic avoidance of obstacles is a dorsal stream function: evidence from optic ataxia. Nat Neurosci 7(7). https://doi.org/10.1038/nn1273
Schoenbaum G, Roesch MR, Stalnaker TA, Takahashi YK (2009) A new perspective on the role of the orbitofrontal cortex in adaptive behaviour. Nat Rev Neurosci 10(12):885–892. https://doi.org/10.1038/nrn2753 Epub 2009 Nov 11
Sereno ME, Trinath T, Augath M, Logothetis NK (2002) Three-dimensional shape representation in monkey cortex. Neuron 33(4):635–652
Shapiro L (2011) The embodied mind. Routledge, New York
Singhal A, Culham JC, Chinellato E, Goodale MA (2007) Dual-task interference is greater in delayed grasping than in visually guided grasping. J Vis 7(5):1–12
Singhal A, Monaco S, Kaufman LD, Culham JC (2013) Human fMRI reveals that delayed action re-recruits visual perception. PLoS One 8(9):2013. https://doi.org/10.1371/journal.pone.0073629 (eCollection 2013)
Smeets JB, Brenner E, Martin J (2009) Grasping Occam’s razor. Adv Exp Med Biol 629:499–522. https://doi.org/10.1007/978-0-387-77064-2_27
Smeets JB, Martin J, Brenner E (2010) Similarities between digits’ movements in grasping, touching and pushing. Exp Brain Res 203(2):339–346. https://doi.org/10.1007/s00221-010-2236-0 Epub 2010 Apr 9
Sutherland A, Crewther DP (2010) Magnocellular visual evoked potential delay with high autism spectrum quotient yields a neural mechanism for altered perception. Brain 133:2089–2097. https://doi.org/10.1093/brain/awq122
Tankus A, Fried I (2012) Visuomotor coordination and motor representation by human temporal lobe neurons. J Cogn Neurosci 24(3):600–610
Theys T, Romero MC, van Loon J, Janssen P (2015) Shape representations in the primate dorsal visual stream. Front Comput Neurosci 9(43). https://doi.org/10.3389/fncom.2015.00043
Tipper SP, Paul M, Hayes A (2006) Vision-for-action: the effects of object property discrimination and action state on affordance compatibility effects. Psychon Bull Rev 13:493–498
Tucker M, Ellis R (1998) On the relations between seen objects and components of potential actions. J Exp Psychol Hum Percept Perform 24:830–846
Turella L, Lignau A (2014) Neural correlates of grasping. Front Hum Neurosci 8(686). https://doi.org/10.3389/fnhum.2014.00686
Vargas P, Paolo ED, Harvey I, Husbands P (eds) (2014) The horizons of evolutionary robotics. MIT Press, Cambridge, MA
Westwood D, Danckert J, Servos P, Goodale M (2002) Grasping two-dimensional images and three-dimensional objects in visual-form agnosia. Exp Brain Res 144(2):262–267
Young G (2006) Are different affordances subserved by different neural pathways? Brain Cogn 62:134–142
Zald DH, Andreotti C (2010) Neuropsychological assessment of the orbital and ventromedial prefrontal cortex. Neuropsychologia 48(12):3377–3391
Zald DH, Rauch SL (2007) The orbitofrontal cortex. Oxford University Press, New York
Zipoli Caiani S, Ferretti G (2016) Semantic and pragmatic integration in vision for action. Conscious Cogn 48:40–54
Author information
Authors and Affiliations
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2019 Springer Nature Switzerland AG (outside the USA)
About this chapter
Cite this chapter
Ferretti, G., Chinellato, E. (2019). Can Our Robots Rely on an Emotionally Charged Vision-for-Action? An Embodied Model for Neurorobotics. In: Vallverdú, J., Müller, V. (eds) Blended Cognition. Springer Series in Cognitive and Neural Systems, vol 12. Springer, Cham. https://doi.org/10.1007/978-3-030-03104-6_5
Download citation
DOI: https://doi.org/10.1007/978-3-030-03104-6_5
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-030-03103-9
Online ISBN: 978-3-030-03104-6
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)