Abstract
In previous chapters, I described the behavioral aspects of fear learning in humans and animals. Öhman et al. hypothesized (Öhman and Mineka 2001, 2003) that the neural mechanisms that process sources of fear (e.g., snakes and spiders), commonly shared among mammals, including humans, are independently maintained in the brain. The snake detection theory (SDT) proposes that the primate brain expanded to be able to detect snakes efficiently during the course of evolution (Isbell 2006, 2009); furthermore, it proposes the existence of an independent fear module in the brain and identifies its neural mechanism in more detail. This chapter will provide a review of the SDT. Before embarking on this review, we will first describe the neural mechanisms underlying general fear learning in relation to typical examples of Pavlovian conditioning through exposure to light and sound as conditioned stimuli (CS).
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References
Acuna C, Gonzales F, Dominguez R (1983) Sensorimotor unit activity related to intention in the pulvinar of the behaving Cebus apella monkeys. Exp Brain Res 52:411–422
Adolphs R, Tranel D, Damasio H, Damasio AR (1995) Fear and the human amygdala. J Neurosci 15:5879–5891
Adolphs R, Gosselin F, Buchanan TW, Tranel D, Schyns P, Damasio AR (2005) A mechanism for impaired fear recognition after amygdala damage. Nature 433:68–72. https://doi.org/10.1038/nature03086
Aggleton JP, Saunders RC (2000) The amygdala- what’s happened in the last decade? In: Aggleton JP (ed) The amygdala: a functional analysis. Oxford University Press, New York, pp 1–30
Amaral DG (2003) The amygdala, social behavior, and danger detection. Ann NY Acad Sci 1000:337–347
Amaral DG, Price JL, Pitkänen A, Carmichael ST (1992) Anatomical organization of the primate amygdaloid complex. In: Aggleton JP (ed) The amygdala: neurobiological aspects of emotion, memory, and mental dysfunction. Wiley-Liss, New York, pp 1–66
Archibald JD (2003) Timing and biogeography of the eutherian radiation: fossils and molecules compared. Mol Phylogenet Evol 28:350–359. https://doi.org/10.1016/S1055-7903(03)00034-4
Arnason U, Gullberg A, Janke A (1998) Molecular timing of primate divergences as estimated by two nonprimate calibration points. J Mol Evol 47:718–727
Baleydier C, Mauguiere F (1987) Network organization of the connectivity between parietal area 7, posterior cingulate cortex and medial pulvinar nucleus: a double fluorescent tracer study in monkey. Exp Brain Res 66:385–393
Barton RA (2004) Binocularity and brain evolution in primates. In: Proceedings of the National Academy of science of the United States of America, vol. 101, pp 10113–10115. https://doi.org/10.1073/pnas.0401955101
Barton RA, Aggleton JP (2000) Primate evolution and the amygdala. In: Aggleton JP (ed) The amygdala: a functional analysis. Oxford University Press, New York, pp 479–508
Barton RA, Aggleton JP, Grenyer R (2003) Evolutionary coherence of the mammalian amygdala. Proc R Soc B Biol Sci 270:539–543. https://doi.org/10.1098/rspb.2002.2276
Bechara A, Tranel D, Damasio H, Adolphs R, Rockland C, Damasio AR (1995) Double dissociation of conditioning and declarative knowledge relative to the amygdala and hippocampus in humans. Science 269:1115–1118
Benevento LA, Miller J (1981) Visual responses of single neurons in the caudal lateral pulvinar of the macaque monkey. J Neurosci 1:1268–1278
Berridge CW, Waterhouse BD (2003) The locus coeruleus-noradrenergic system: modulation of behavioral state and state-dependent cognitive processes. Brain Res Rev 42:33–84
Berson DM (1988) Retinal and cortical inputs to cat superior colliculus: composition, convergence and laminar specificity. In: Hicks TP, Benedek G (eds) Progress in brain research, vol 75, pp 17–26. https://doi.org/10.1016/S0079-6123(08)60462-8
Cadle JE (1988) Phylogenetic relationships among advanced snakes: a molecular perspective, University of California Publications in Zoology, vol 119. University of California Press, Berkeley
Casagrande VA (1994) A third parallel visual pathway to primate area V1. Trends Neurosci 17:305–310. https://doi.org/10.1016/0166-2236(94)90065-5
Casanova C (2004) The visual functions of the pulvinar. In: Chalupa LM, Werner JS (eds) The visual neurosciences. MIT Press, Cambridge, MA, pp 592–608
Chalupa LM (1991) Visual function of the pulvinar. In: Leventhal AG (ed) The neural basis of visual function. CRC Press, Boca Raton, pp 140–159
Chaves R, Sampaio I, Schneider MP, Schneider H, Page SL, Goodman M (1999) The place of Callimico goeldii in the callitrichine phylogenetic tree: evidence from von Willebrand factor gene intron II sequences. Mol Phylogenet Evol 13:392–404. https://doi.org/10.1006/mpev.1999.0658
Cheney DL, Wrangham RW (1987) Predation. In: Smuts BB, Cheney DL, Seyfarth RM, Wrangham RW, Struhsaker TT (eds) Primate societies. University of Chicago Press, Chicago, pp 227–239
Corbetta M, Miezin FM, Dobmeyer S, Shulman GL, Petersen SE (1991) Selective and divided attention during visual discriminations of shape, color, and speed: functional anatomy by positron emission tomography. J Neurosci 11:2382–2402
Coss RG (2003) The role of evolved perceptual biases in art and design. In: Voland E, Grammer K (eds) Evolutionary aesthetics. Springer, New York, pp 69–130
Crompton RH (1995) “Visual predation”, habitat structure, and the ancestral primate niche. In: Alterman L, Doyle G, Izard MK (eds) Creatures of the dark: the nocturnal prosimians. Plenum Press, New York, pp 11–30
Cropp S, Boinski S (2000) The central American squirrel monkey (Saimiri oerstedii): introduced hybrid or endemic species? Mol Phylogenet Evol 16:350–365. https://doi.org/10.1006/mpev.2000.0814
Dawkins R (1982) The expanded phenotype: the gene as the unit of selection. Freeman, San Francisco
Ellard CG, Goodale MA (1988) A functional analysis of the collicular output pathways: a dissociation of deficits following lesions of the dorsal tegmental decussation and the ipsilateral collicular efferent bundle in the Mongolian gerbil. Exp Brain Res 71:307–319
Feduccia A (1995) “Big bang” for tertiary birds? Trends Ecol Evol 18:172–176. https://doi.org/10.1016/S0169-5347(03)00017-X
Glaw F, Vences M (1994) A field guide to the amphibians and reptiles of Madagascar, 2nd edn. Vences & Glaw, Verlags GbR, Cologne
Glendenning KK, Hall JA, Diamond IT, Hall WC (1975) The pulvinar nucleus of Galago senegalensis. J Comp Neurol 161:419–457. https://doi.org/10.1002/cne.901610309
Goodale MA, Milner AD (1992) Separate visual pathways for perception and action. Trends Neurosci 15:20–25. https://doi.org/10.1016/0166-2236(92)90344-8
Goodale MA, Westwood DA (2004) An evolving view of duplex vision: separate but interacting cortical pathways for perception and action. Curr Opin Neurobiol 14:203–211. https://doi.org/10.1016/j.conb.2004.03.002
Greene HW (1983) Dietary correlates of the origin and radiation of snakes. Am Zool 23:431–441. https://doi.org/10.1093/icb/23.2.431
Greene HW (1997) Snakes: the evolution of mystery in nature. University of California Press, Berkeley
Greene HW, Burghardt GM (1978) Behavior and phylogeny: constriction in ancient and modern snakes. Science 200:74–77. https://doi.org/10.1126/science.635575
Gutierrez C, Cola MG, Seltzer B, Cusick C (2000) Neurochemical and connectional organization of the dorsal pulvinar complex in monkeys. J Comp Neurol 419:61–86
Hainsworth FR, Overmier JB, Snowdon CT (1967) Specific and permanent deficits in instrumental avoidance responding following forebrain ablation in the goldfish. J Comp Physiol Psychol 63(1):111–116. https://doi.org/10.1037/h0024143
Hamann SB, Adolphs R (1999) Normal recognition of emotional similarity between facial expressions following bilateral amygdala damage. Neuropsychologia 37:1135–1141. https://doi.org/10.1016/S0028-3932(99)00027-5
Hendry SHC, Reid RC (2000) The koniocellular pathway in primate vision. Annu Rev Neurosci 23:127–153. https://doi.org/10.1146/annurev.neuro.23.1.127
Hendry SHC, Yoshioka T (1994) A neurochemically distinct third channel in the macaque dorsal lateral geniculate nucleus. Science 264:575–577. https://doi.org/10.1126/science.8160015
Henry GH, Vidyasagar TR (1991) Evolution of mammalian visual pathways. In: Cronly-Dillon JR, Gregory RL (eds) Evolution of the eye and visual system: vision and visual dysfunction, vol 2. CRC Press, Boca Raton, pp 442–465
Ignashchenkova A, Dicke PW, Haarmeier T, Their P (2004) Neuron-specific contribution of the superior colliculus to overt and covert shifts of attention. Nat Neurosci 7:56–64. https://doi.org/10.1038/nn1169
Isbell LA (1994) Predation on primates: ecological patterns and evolutionary consequences. Evol Anthropol 3:61–71. https://doi.org/10.1002/evan.1360030207
Isbell LA (2006) Snakes as agents of evolutionary change in primate brains. J Hum Evol 51:1–35. https://doi.org/10.1016/j.jhevol.2005.12.012
Isbell LA (2009) The fruit, the tree, and the serpent: why we see so well. Harvard University Press, New York
Jones EG (1985) The thalamus. Plenum Press, New York
Jones EG, Burton H (1976) A projection from the medial pulvinar to the amygdala in primates. Brain Res 104:142–147
Kaas JH, Huerta MF (1988) The subcortical visual system of primates. In: Steklis HD, Erwin J (eds) Comparative primate biology, vol 4. Alan R. Liss, New York, pp 327–391
Kadoya S, Wolin LR, Massopust LC Jr (1971) Photically evoked unit activity in the tectum opticum of the squirrel monkey. J Comp Neurol 142:495–508. https://doi.org/10.1002/cne.901420407
Kalin NH, Shelton SE, Davidson RJ (2004) The role of the central nucleus of the amygdala in mediating fear and anxiety in the primate. J Neurosci 24:5506–5515. https://doi.org/10.1523/JNEUROSCI.0292-04.2004
Kanaseki T, Spragne J (1974) Anatomical organization of pretectal nuclei and tectal laminae in the cat. J Comp Neurol 158:319–337. https://doi.org/10.1002/cne.901580307
Kapp BS, Pascoe JP, Bixler MA (1984) The amygdala: a neuroanatomical systems approach to its contribution to aversive conditioning. In: Butters N, Squire LR (eds) Neuropsychology of memory. Guilford Press, New York, pp 473–488
Kapp BS, Wilson A, Pascoe JP, Supple WF, Whalen PJ (1990) A neuroanatomical systems analysis of conditioned bradycardia in the rabbits. In: Gabriel MR, Moore JW (eds) Learning and computational neuroscience: foundations of adaptative networks. MIT Press, Cambridge, MA, pp 53–90
Kardong KV (2002) Colubrid snakes and Duvernoy’s “venom” glands. J Toxicol: Toxin Rev 21:1–19. https://doi.org/10.1081/TXR-120004739
Kastner S, De Weerd P, Ungerleider LG (2000) Texture segregation in the human visual cortex: a functional MRI study. J Neurophysiol 83:2453–2457
Kastner S, O’Connor DH, Fukui MM, Fehd HM, Herwig U, Pinsk MA (2004) Functional imaging of the human lateral geniculate nucleus and pulvinar. J Neurophysiol 91:438–448. https://doi.org/10.1152/jn.00553.2003
Kawai N (2008) Crossmodal spatial attention shift produced by centrally presented gaze cues. Jpn Psychol Res 50:100–103. https://doi.org/10.1111/j.1468-5884.2008.00366.x
Kawai N (2011) Attentional shift by eye gaze requires joint attention: eye gaze cues are unique to shift attention. Jpn Psychol Res 53:292–301. https://doi.org/10.1111/j.1468-5884.2011.00470.x
Kawai N, Kono R, Sugimoto S (2004) Avoidance learning in the crayfish (Procambarus clarkii) depends on the predatory imminence of the unconditioned stimulus: a behavior systems approach to learning in invertebrates. Behav Brain Res 150:229–237. https://doi.org/10.1016/S0166-4328(03)00261-4
Kawai N, Kubo K, Masataka N, Hayakawa S (2016) Conserved evolutionary history for quick detection of threatening faces. Anim Cogn 19:655–660. https://doi.org/10.1007/s10071-015-0949-y
Kingdon J (1997) The kingdom field guide to African mammals. Academic, San Diego
Klier EM, Wang H, Crawford JD (2003) Three-dimensional eye-head coordination is implemented downstream from the superior colliculus. J Neurophysiol 89:2839–2853. https://doi.org/10.1152/jn.00763.2002
Klüver H, Bucy PC (1937) “Psychic blindness” and other symptoms following bilateral temporal lobectomy in rhesus monkeys. Am J Physiol 119:352–353
LaBerge D, Buchsbaum MS (1990) Positron emission tomographic measurements of pulvinar activity during an attention task. J Neurosci 10:613–619
LeDoux JE (1996) The emotional brain: the mysterious underpinnings emotional life. Simon and Schuster, New York
LeDoux J (2000) The amygdala and emotion: a view through fear. In: Aggleton JP (ed) The amygdala: a functional analysis. Oxford University Press, New York, pp 281–310
LeDoux JE (2002) Synaptic self: how our brains become who we are. Viking, New York
LeDoux JE (2004) Coming to terms with fear. Proc Natl Acad Sci USA 111:2871–2878. https://doi.org/10.1073/pnas.1400335111
LeDoux JE (2015) Anxious: using the brain to understand and treat fear and anxiety. Viking, New York
LeDoux JE, Sakaguchi A, Reis DJ (1984) Subcortical efferent projections of the medial geniculate nucleus mediate emotional responses conditioned to acoustic stimuli. J Neurosci 4:683–698
LeDoux JE, Farb C, Ruggiero DA (1990) Topographic organization of neurons in the acoustic thalamus that project to the amygdala. J Neurosci 10:1043–1054
Madsen O, Scalley M, Douady CJ, Kao DJ, DeBry RW, Adkins R, Amrine HM, Stanhope MJ, de Jong WW, Springer MS (2001) Parallel adaptive radiations in two major clades of placental mammals. Nature 409:610–614. https://doi.org/10.1038/35054544
Martin LD (1989) Fossil history of the terrestrial Carnivora. In: Gittleman JL (ed) Carnivore behavior, ecology, and evolution. Cornell University Press, Ithaca, pp 536–568
May PJ (2006) The mammalian superior colliculus: laminar structure and connections. In: Progress in brain research, vol 151, pp 321–378. https://doi.org/10.1016/S0079-6123(05)51011-2
McGrew WC (2015) Snakes as hazards: modeling risk by chasing chimpanzees. Primates 56:107–111
Murphy WJ, Eizirik E, O’Brien SJ, Madsen O, Scally M, Douady CJ, Teeling E, Ryder OA, Stanhope MJ, de Jong WW, Springer MS (2001a) Resolution of the early placental mammal radiation using Bayesian phylogenetics. Science 294:2348–2351. https://doi.org/10.1126/science.1067179
Murphy WJ, Eizirik E, Johnson WE, Zhang YP, Ryder OA, O’Brien SJ (2001b) Molecular phylogenetics and the origins of placental mammals. Nature 409:614–618. https://doi.org/10.1038/35054550
Neophytou SI, Aspley S, Butler S, Beckett S, Marsden CA (2001) Effects of lesioning noradrenergic neurones in the locus coeruleus on conditioned and unconditioned aversive behaviour in the rat. Prog Neuro-Psychopharmacol Biol Psychiatry 25:1307–1321
Northmore OPM, Levine ES, Schneider GE (1988) Behavior evoked by electrical stimulation of the hamster superior colliculus. Exp Brain Res 73:595–605
Öhman A, Mineka S (2001) Fears, phobias, and preparedness: toward an evolved module of fear and fear learning. Psychol Rev 108:483–522. https://doi.org/10.1037//0033-295X.108.3.483
Öhman A, Mineka S (2003) The malicious serpent: snakes as a prototypical stimulus for an evolved module of fear. Curr Dir Psychol Sci 12:5–9
Okamoto-Barth S, Kawai N (2006) The role of attention in the facilitation effect and another “inhibition of return”. Cognition 101:B42–B50. https://doi.org/10.1016/j.cognition.2005.11.002
Overmier JB, Papini MR (1986) Factors modulating the effects of teleost telencephalon ablation on retention, relearning, and extinction of instrumental avoidance behavior. Behav Neurosci 100:190–199. https://doi.org/10.1037/0735-7044.100.2.190
Panksepp J (1982) Toward a general psychological theory of emotions. Behav Brain Sci 5(3):407–422
Panksepp J (2010) Affective neuroscience of the emotional BrainMind: evolutionary perspectives and implications for understanding depression. Dialogues Clin Neurosci 12(4):533–545. https://doi.org/10.1017/S0140525X00012759
Pavlov IP (1928) Lectures on conditioned reflexes (trans: Gantt WH). Allen and Unwin, London
Peterhans E, von der Heydt R (1993) Functional organization of area V2 in the alert macaque. Eur J Neurosci 5:509–524. https://doi.org/10.1111/j.1460-9568.1993.tb00517.x
Petersen SE, Robinson DL, Keys W (1985) Pulvinar nuclei of the behaving rhesus monkey: visual responses and their modulation. J Neurophysiol 54:867–886
Petersen SE, Robinson DL, Morris JD (1987) Contributions of the pulvinar to visual spatial attention. Neuropsychologia 25:97–105. https://doi.org/10.1016/0028-3932(87)90046-7
Pessoa L, Adolphs R (2010) Emotion processing and the amygdala: from a ‘low road’ to ‘many roads’ of evaluating biological significance. Nat Rev Neurosci 11:773–783. https://doi.org/10.1038/nrn2920
Rafal RD, Posner MI (1987) Deficits in human visual spatial attention following thalamic lesions. Proc Natl Acad Sci USA 84:7349–7353
Reyes A, Gissi C, Catzeflis F, Nevo E, Pesole G, Saccone C (2004) Congruent mammalian trees from mitochondrial and nuclear genes using Bayesian methods. Mol Biol Evol 21:397–403. https://doi.org/10.1093/molbev/msh033
Robinson DA (1972) Eye movements evoked by collicular stimulation in the alert monkey. Vis Res 12:1795–1808. https://doi.org/10.1016/0042-6989(72)90070-3
Robinson DL, Petersen SE (1992) The pulvinar and visual salience. Trends Neurosci 15:127–132. https://doi.org/10.1016/0166-2236(92)90354-B
Robinson DL, Petersen SE, Keys W (1986) Saccade-related activity in the pulvinar nuclei of the behaving rhesus monkey. Exp Brain Res 62:625–634
Ross CF (2000) Into the light: the origin of anthropoidea. Annu Rev Anthropol 29:147–194. https://doi.org/10.1146/annurev.anthro.29.1.147
Sah P, Faber ESL, Lopez De Armentia M, Power J (2003) The amygdaloid complex: anatomy and physiology. Physiol Rev 83:803–834. https://doi.org/10.1152/physrev.00002.2003
Schneider H, Schneider MPC, Sampaio I, Harada ML, Stanhope M, Czelusniak J, Goodman M (1993) Molecular phylogeny of the New World monkeys (Platyrrhini, Primates). Mol Phylogenet Evol 2:225–242. https://doi.org/10.1006/mpev.1993.1022
Schneider H, Canavez FC, Sampaio I, Moreira MAM, Tagliaro CH, Seua’nez HN (2001) Can molecular data place each neotropical monkey in its own branch? Chromosoma 109:515–523. https://doi.org/10.1007/s004120000106
Selemon LD, Goldman-Rakic PS (1988) Common cortical and subcortical targets of the dorsolateral prefrontal and posterior parietal cortices in the rhesus monkey: evidence for a distributed neural network subserving spatially guided behavior. J Neurosci 8:4049–4068
Sewards TV, Sewards MA (2002) Innate visual object recognition in vertebrates: some proposed pathways and mechanisms. Comp Biochem Physiol A Mol Integr Physiol 132:861–891
Sherman SM, Spear PD (1982) Organization of visual pathways in normal and visually deprived cats. Physiol Rev 62:738–855
Sibley CG, Ahlquist JE (1990) Phylogeny and classification of birds: a study in molecular evolution. Yale University Press, New Haven
Soares JGM, Diogo ACM, Fiorani M, Souza APB, Gattass R (2001) Changes in orientation and direction selectivity of cells in secondary visual area (V2) after GABA inactivation of the pulvinar in Cebus monkeys. Soc Neurosci Abstr 27:1633
Springer MS, Murphy WJ, Eizirik E, O’Brien SJ (2003) Placental mammal diversification and the cretaceous-tertiary boundary. Proc Natl Acad Sci USA 100:1056–1061. https://doi.org/10.1073/pnas.0334222100
Springer MS, Stanhope MJ, Madsen O, de Jong WW (2004) Molecules consolidate the placental mammal tree. Trends Ecol Evol 19:430–438. https://doi.org/10.1016/j.tree.2004.05.006
Stein BE (1978) Nonequivalent visual, auditory, and somatic corticotectal influences in cat. J Neurophysiol 41:55–64
Stepniewska I (2004) The pulvinar complex. In: Kaas JH, Collins CE (eds) The primate visual system. CRC Press, Boca Raton, pp 53–80. https://doi.org/10.1201/9780203507599.ch3
Stepniewska I, Qi H-X, Kaas JH (1999) Do superior colliculus projection zones in the inferior pulvinar project to MT in primates? Eur J Neurosci 11:469–480. https://doi.org/10.1046/j.1460-9568.1999.00461.x
Stepniewska I, Qi H-X, Kaas JH (2000) Projections of the superior colliculus to subdivisions of the inferior pulvinar in new world and old world monkeys. Vis Neurosci 17:529–549. https://doi.org/10.1017/S0952523800174048
Tinbergen N (1951) The study of instinct. Oxford University Press, New York
Trojanowski JQ, Jacobson S (1974) Medial pulvinar afferents to frontal eye fields in rhesus monkey demonstrated by horseradish peroxidase. Brain Res 80:395–411. https://doi.org/10.1016/0006-8993(74)91025-7
Van Le Q, Isbell LA, Matsumoto J, Nguyen M, Hori E, Maior RS, Tomaz C, Tran AH, Ono T, Nishijo H (2013) Pulvinar neurons reveal neurobiological evidence of past selection for rapid detection of snakes. Proc Natl Acad Sci USA 110:19000–19005. https://doi.org/10.1073/pnas.1312648110
Vidal N (2002) Colubroid systematics: evidence for an early appearance of the venom apparatus followed by extensive evolutionary tinkering. J Toxicol: Toxin Rev 21:21–41. https://doi.org/10.1081/TXR-120004740
Villeneuve MY, Kupers R, Gjedde A, Ptito M, Casanova C (2005) Pattern-motion selectivity in the human pulvinar. NeuroImage 28:474–480. https://doi.org/10.1016/j.neuroimage.2005.06.015
Waddell PJ, Shelley S (2003) Evaluating placental inter-ordinal phylogenies with novel sequences including RAG1, gamma-fibrinogen, ND6, and mt-tRNA, plus MCMC-driven nucleotide, amino acid, and codon models. Mol Phylogenet Evol 28:197–224
Warner CE, Kwan WC, Bourne JA (2012) The early maturation of visual cortical area MT is dependent on input from the retinorecipient medial portion of the inferior pulvinar. J Neurosci 32:17073–17085. https://doi.org/10.1523/JNEUROSCI.3269-12.2012
Warner CE, Kwan WC, Wright D, Johnston LA, Egan GF, Bourne JA (2015) Preservation of vision by the pulvinar following early-life primary visual cortex lesions. Curr Biol 25:424–434. https://doi.org/10.1016/j.cub.2014.12.028
Wayne RK, Benveniste RE, Janczewski DN, O’Brien SJ (1989) Molecular and biochemical evolution of the Carnivora. In: Gittleman JL (ed) Carnivore behavior, ecology, and evolution. Cornell University Press, Ithaca, pp 465–494
White BJ, Berg DJ, Kan JY, Marino RA, Itti L, Munoz DP (2017) Superior colliculus neurons encode a visual saliency map during free viewing of natural dynamic video. Nat Commun 8:14263. https://doi.org/10.1038/ncomms14263
Zamudio KR, Greene HW (1997) Phylogeography of the bushmaster (Lachesis muta: Viperidae): implications for neotropical biogeography, systematics, and conservation. Biol J Linn Soc 62:421–442. https://doi.org/10.1111/j.1095-8312.1997.tb01634.x
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Kawai, N. (2019). The Underlying Neuronal Circuits of Fear Learning and the Snake Detection Theory (SDT). In: The Fear of Snakes. The Science of the Mind. Springer, Singapore. https://doi.org/10.1007/978-981-13-7530-9_3
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