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Referencias:

• Barnes, W.J.P., Nalbach, H.O., Eye movements in freely moving crabs: Their sensory basis and possible role in flow-field analysis (1993) Comp Biochem Physiol, 104, pp. 675-693
• Bengochea, M., Berón de Astrada, M., Tomsic, D., Sztarker, J., A crustacean lobula plate: Morphology, connections, and retinotopic organization (2018) J Comp Neurol, 526
• Berón de Astrada, M., Tomsic, D., Physiology and morphology of visual movement detector neurons in a crab (Decapoda: Brachyura) (2002) J Comp Physiol a Neuroethol Sens Neural Behav Physiol, 188, pp. 539-551
• Berón de Astrada, M., Medan, V., Tomsic, D., How visual space maps in the optic neuropils of a crab (2011) J Comp Neurol, 519, pp. 1631-1639
• Berón de Astrada, M., Bengochea, M., Medan, V., Tomsic, D., Regional-ization in the eye of the grapsid crab Neohelice granulata (=Chasmag-nathus granulatus): Variation of resolution and facet diameters (2012) J Comp Physiol a Neuroethol Sens Neural Behav Physiol, 198, pp. 173-180
• Berón de Astrada, M., Bengochea, M., Sztarker, J., Delorenzi, A., Tomsic, D., Behaviorally related neural plasticity in the arthropod optic lobes (2013) Curr Biol, 23, pp. 1389-1398
• Collet, T.S., Binocular depth vision in arthropods (1987) Trends Neurosci, 10, pp. 1-2
• Devoe, R.D., Kaiser, W., Ohm, J., Stone, L.S., Horizontal movement detectors of honeybees: Directionally-selective visual neurons in the lobula and brain (1982) J Comp Physiol a Neuroethol Sens Neural Behav Physiol, 147, pp. 155-170
• Duistermars, B.J., Care, R.A., Frye, M.A., Binocular interactions underlying the classic optomotor responses of flying flies (2012) Front Behav Neurosci, 6, p. 6
• Dunbier, J.R., Wiederman, S.D., Shoemaker, P.A., O’Carroll, D.C., Facilitation of dragonfly target-detecting neurons by slow moving features on continuous paths (2012) Front Neural Circuits, 6 (79)
• Hemmi, J.M., Zeil, J., Robust judgement of inter-object distance by an arthropod (2003) Nature, 421
• Hennig, P., Kern, R., Egelhaaf, M., Binocular integration of visual information: A model study on naturalistic optic flow processing (2011) Front Neural Circuits, 5, p. 4. , CrossRef Medline
• Horridge, G.A., Sandeman, D.C., Nervous control of optokinetic responses in the crab, Carcinus (1964) Proc R Soc Lond B Biol Sci, 161, pp. 216-246
• Hubel, D.H., Wiesel, D.T.N., Receptive fields, binocular interaction and functional architecture in the cat’s visual cortex (1962) J Physiol, 160
• Krapp, H.G., Hengstenberg, R., Egelhaaf, M., Binocular contributions to optic flow processing in the fly visual system (2001) J Neurophysiol, 85
• Land, M., Layne, J., The visual control of behavior in fiddler crabs: II. Tracking control systems in courtship and defense (1995) J Comp Physiol a Neuroethol Sens Neural Behav Physiol, 177, pp. 91-103
• Livingstone, M.S., Conway, B.R., Substructure of direction-selective receptive fields in macaque V1 (2003) J Neurophysiol, 89, pp. 2743-2759
• Luppi, T., Bas, C., Méndez Casariego, A., Albano, M., Lancia, J., Kittlein, M., Rosenthal, A., Iribarne, O., The influence of habitat, season and tidal regime in the activity of the intertidal crab Neohelice (=Chasmagnathus) granulata (2013) Helgol Mar Res, 67, pp. 1-15
• Medan, V., Oliva, D., Tomsic, D., Characterization of lobula giant neurons responsive to visual stimuli that elicit escape behaviors in the crab Chasmagnathus (2007) J Neurophysiol, 98
• Medan, V., Berón De Astrada, M., Scarano, F., Tomsic, D., A network of visual motion-sensitive neurons for computing object position in an arthropod (2015) J Neurosci, 35
• Nalbach, H.O., Thier, P., Varjú, D., Binocular interaction in the optokinetic system of the crab Carcinus maenas (L.): Optokinetic gain modified by bilateral image flow (1993) Vis Neurosci, 10, pp. 873-885
• Nityananda, V., Tarawneh, G., Rosner, R., Nicolas, J., Crichton, S., Read, J., Insect stereopsis demonstrated using a 3D insect cinema (2016) Sci Rep, 6
• Oliva, D., Tomsic, D., Computation of object approach by a system of visual motion-sensitive neurons in the crab Neohelice (2014) J Neurophysiol, 112, pp. 1477-1490
• Oliva, D., Tomsic, D., Object approach computation by a giant neuron and its relation with the speed of escape in the crab Neohelice (2016) J Exp Biol, 219
• Ramdya, P., Engert, F., Emergence of binocular functional properties in a monocular neural circuit (2008) Nat Neurosci, 11, pp. 1083-1090
• Rosner, R., Homberg, U., Widespread sensitivity to looming stimuli and small moving objects in the central complex of an insect brain (2013) J Neurosci, 33, pp. 8122-8133
• Sal Moyano, M.P., Gavio, M.A., McLay, C.L., Luppi, T., Variation in the post-copulatory guarding behavior of Neohelice granulata (Brachyura, Grapsoidea, Varunidae) in two different habitats (2014) Mar Ecol, 36, pp. 1185-1194
• Scarano, F., Tomsic, D., Escape response of the crab Neohelice to computer generated looming and translational visual danger stimuli (2014) J Physiol Paris, 108, pp. 141-147
• Smolka, J., Hemmi, J.M., Topography of vision and behaviour (2009) J Exp Biol, 212, pp. 3522-3532
• Sombke, A., Harzsch, S., Immunolocalization of histamine in the optic neuropils of Scutigera coleoptrata (Myriapoda: Chilopoda) reveals the basal organization of visual systems in mandibulata (2015) Neurosci Lett, 594, pp. 111-116
• Strausfeld, N.J., Brain organization and the origin of insects: An assessment (2009) Proc Biol Sci, 276
• Strausfeld, N.J., Nässel, D.R., Neuroarchitecture of brain regions that subserve the compound eyes of Crustacea and insect (1981) Handbook of Sensory Physiology: Vision in Invertebrates, VII/6B, pp. 1-32. , (Autrum, ed), Berlin; Heidelberg; New York: Springer
• Suver, M.P., Huda, A., Iwasaki, N., Safarik, S., Dickinson, M.H., An array of descending visual interneurons encoding self-motion in Drosophila (2016) J Neurosci, 36
• Suzuki, Y., Morimoto, T., Miyakawa, H., Aonishi, T., Cooperative integration and representation underlying bilateral network of fly motion-sensitive neurons (2014) Plos One, 9
• Sztarker, J., Tomsic, D., Binocular visual integration in the crustacean nervous system (2004) J Comp Physiol a Neuroethol Sens Neural Behav Physiol, 190, pp. 951-962
• Sztarker, J., Tomsic, D., Brain modularity in arthropods: Individual neurons that support “what” but not “where” memories (2011) J Neurosci, 31, pp. 8175-8180
• Tomsic, D., Visual motion processing subserving behavior in crabs (2016) Curr Opin Neurobiol, 41, pp. 113-121
• Tomsic, D., Berón de Astrada, M., Sztarker, J., Identification of individual neurons reflecting short-and long-term visual memory in an arthropod (2003) J Neurosci, 23, pp. 8539-8546
• Tomsic, D., Sztarker, J., Berón de Astrada, M., Oliva, D., Lanza, E., The predator and prey behaviors of crabs: From ecology to neural adaptations (2017) J Exp Biol, 220
• Wertz, A., Borst, A., Haag, J., Nonlinear integration of binocular optic flow by DNOVS2, a descending neuron of the fly (2008) J Neurosci, 28, pp. 3131-3140
• Wiersma, C.A., Bush, B.M., Waterman, T.H., Efferent visual responses of contralateral origin in the optic nerve of the crab podophthalmus (1964) J Cell Comp Physiol, 64
• Wood, H.L., Glantz, R.M., Distributed processing by visual interneurons of crayfish brain. I. response characteristics and synaptic interactions (1980) J Neurophysiol, 43
• Wood, H.L., Glantz, R.M., Distributed processing by visual interneurons of crayfish brain: II. Network organization and stimulus modulation of synaptic efficacy (1980) J Neurophysiol, 43, pp. 741-753
• Zeil, J., Hemmi, J.M., The visual ecology of fiddler crabs (2006) J Comp Physiol A, 192, pp. 1-25

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