Book contents
- The Thalamus
- The Thalamus
- Copyright page
- Contents
- Contributors
- Preface
- Section 1: History
- Section 2: Anatomy
- Section 3: Evolution
- Chapter 5 Morphological, Developmental, and Functional Evolution of the Thalamus
- Chapter 6 Lamprey Thalamus and Beyond
- Section 4: Development
- Section 5: Sensory Processing
- Section 6: Motor Control
- Section 7: Cognition
- Section 8: Arousal
- Section 9: Computation
- Index
- References
Chapter 5 - Morphological, Developmental, and Functional Evolution of the Thalamus
from Section 3: - Evolution
Published online by Cambridge University Press: 12 August 2022
Edited by
Book contents
- The Thalamus
- The Thalamus
- Copyright page
- Contents
- Contributors
- Preface
- Section 1: History
- Section 2: Anatomy
- Section 3: Evolution
- Chapter 5 Morphological, Developmental, and Functional Evolution of the Thalamus
- Chapter 6 Lamprey Thalamus and Beyond
- Section 4: Development
- Section 5: Sensory Processing
- Section 6: Motor Control
- Section 7: Cognition
- Section 8: Arousal
- Section 9: Computation
- Index
- References
Summary
The thalamus traditionally is divided into the dorsal and ventral divisions, with both divisions divided into groups of nuclei. More recent approaches have defined divisions based on functional features, development, and/or evolutionary relationships. The thalamic nuclei are inextricably related to the corresponding divisions of the telencephalon, which is now recognized to have four developmental pallial sectors (the medial sector–derived hippocampal cortices; dorsal sector–derived neocortex; and lateral and ventral sector–derived claustrum, pallial amygdala, and related lateral nuclei in mammals) and the subpallium (which includes the septal nuclei, subpallial amygdala, and basal ganglia in mammals). The two evolutionary divisions of the dorsal thalamus, present in all jawed vertebrates, are the lemnothalamus and collothalamus. In amniotes, elaboration of different pallial sectors and their related dorsal thalamic nuclei was divergent, with the lemnothalamic-related, allocentric spatial mapping abilities selected for early in the line to mammals and the collothalamic-related, egocentric spatial mapping abilities selected for early in the line to reptiles, including birds. Secondarily, the collothalamic system was elaborated in mammals (e.g., LP/pulvinar in primates) and the lemnothalamic system in reptiles (e.g., primary visual and somatosensory nuclei in birds). Commonalities of thalamotelencephalic circuit motifs evolved in both lineages, supporting the functions of complex cognition and consciousness.
Keywords
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- Chapter
- Information
- The Thalamus , pp. 91 - 124Publisher: Cambridge University PressPrint publication year: 2022
References
Aboitiz, F., Morales, D., & Montiel, J. (2003) The evolutionary origin of the mammalian neocortex: towards an integrated developmental and functional approach. Behav Brain Sci 26:535–586.CrossRefGoogle ScholarPubMed
Agrillo, C., & Bisazza, A. (2017) Understanding the origin of number sense: a review of fish studies. Phil Trans Roy Soc B 373:20160511. doi:10.1098/rstb.2016.0511.CrossRefGoogle Scholar
Agrillo, A., Petrazzini, M.E., & Dadda, M. (2013) Illusory patterns are fishy for fish, too. Front Neur Circ 7. doi:10.3389/fncir.2013.00137.Google Scholar
Atoji, Y., Sarkar, S., & Wild, J.M. (2016) Proposed homologue of the dorsomedial subdivision and V-shaped layer of the avian hippocampus to Ammon’s horn and dentate gyrus, respectively. Hipp 26:1608–1617.CrossRefGoogle Scholar
Baars, B.J. (2003) Working memory requires conscious processes, not vice versa. In: Osaka, N. (Ed.), Neural Basis of Consciousness. John Benjamins Publishing Co., Amsterdam, pp. 11–26.Google Scholar
Bachy, I., Vernier, P., & Rétaux, S. (2001) The LIM-homeodomain gene family in the developing Xenopus brain: conservation and divergences with the mouse related to the evolution of the forebrain. J Neurosci 21:7620–7629.CrossRefGoogle Scholar
Baldwin, M.K.L., Balaram, P., and Kaas, J.H. (2017) The evolution and functions of nuclei of the visual pulvinar in primates. J Comp Neurol 525:3207–3226.Google Scholar
Belekhova, M.G., Kratskin, I.L., Repérant, J., Pierre, J., Vesselkin, N.P., Kenigfest, N.B., Tumanova, N.L., & Chkheidze, D.D. (1991) Localization of GABA-immunoreactive elements in the thalamus of the tortoise Emys orbicularis. Zh Evol Biokhim Fiziol 27:676–685.Google Scholar
Belgard, T.G., Montiel, J.F., Wang, W.Z., García-Moreno, F., Margulies, E.H., Ponting, C.P., & Molnár, Z. (2013) Adult pallial transcriptomes surprise in not reflecting predicted homologies across diverse chicken and mouse pallial sectors. Proc Nat Acad Sci 110:13150–13155.Google Scholar
Bickford, M.E. (2016) Thalamic circuit diversity: modulation of the driver/modulator framework. Front Neural Circ 9, Art. 86, doi:10.3389/fncir.2015.00086.Google Scholar
Bielle, F., Marcos-Mondejar, P., Keita, M., Mailhes, C., Verney, C., Nguyen Ba-Chavet, K., Tessier-Lavigne, M., Lopez-Bendito, G., & Garel, S. (2011) Slit2 activity in the migration of guidepost neurons shapes thalamic projections during development and evolution. Neuron 69:1085–1098.Google Scholar
Bingman, V.P., Rodríguez, F., & Salas, C. (2017) The hippocampus of nonmammalian vertebrates. In: Kaas, J.H., & Striedter, G. (Eds.), Evolution of Nervous Systems. Vol. 1: The Evolution of the Nervous Systems in Nonmammalian Vertebrates, 2nd ed. Elsevier, Amsterdam, pp. 479–489.Google Scholar
Braford, M.R., Jr. (1995) Comparative aspects of forebrain organization in the ray-finned fishes: touchstone or not? Brain Behav Evol 46:259–274.Google Scholar
Briscoe, S.D., Albertin, C.B., Rowell, J.J., & Ragsdale, C.W. (2018) Neocortical association cell types in the forebrain of birds and alligators. Curr Biol 28:686–696.Google Scholar
Broglio, C., Rodriguez, F., Gomez, A., Arias, J.L., & Salas, C. (2010) Selective involvement of goldfish lateral pallium in spatial memory. Behav Brain Res 210:191–201.CrossRefGoogle ScholarPubMed
Brown, M., Keynes, R., & Lumsden, A. (2001) The Developing Brain. Oxford University Press, Oxford, UK.Google Scholar
Bruce, L.L., & Butler, A.B. (1984) Telencephalic connections in lizards. I. Projections to cortex. J Comp Neurol 229:585–601.Google Scholar
Bruce, L.L., & Neary, T. (1995) The limbic system of tetrapods: a comparative analysis of cortical and amygdalar populations. Brain Behav Evol 46:224–234.Google Scholar
Bulchand, S., Grove, E.A., Porter, F.D., & Tole, S. (2001) LIM-homeodomain gene Lhx2 regulates the formation of the cortical hem. Mech Dev 100:165–175.CrossRefGoogle ScholarPubMed
Butler, A.B. (1994a) The evolution of the dorsal pallium in the telencephalon of amniotes: cladistic analysis and a new hypothesis. Brain Res Rev 19:66–101.Google Scholar
Butler, A.B. (1994b) The evolution of the dorsal thalamus of jawed vertebrates, including mammals: cladistic analysis and a new hypothesis. Brain Res Rev 19:29–65.Google Scholar
Butler, A.B. (1995) The dorsal thalamus of jawed vertebrates: a comparative viewpoint. Brain Behav Evol 46:209–223.Google Scholar
Butler, A.B. (2007) The dual elaboration hypothesis of the evolution of the dorsal thalamus. In Krubitzer, L.A., & Kaas, J.H. (Eds.), Evolution of Nervous System in Mammals. Elsevier, Amsterdam, pp. 517–523.Google Scholar
Butler, A.B. (2008a) Evolution of brains, cognition, and consciousness. Brain Res Bull 75:442–449.Google Scholar
Butler, A.B. (2008b) Evolution of the dorsal thalamus: a morphological-functional review. Thalamus Relate Sys 4:35–58.Google Scholar
Butler, A. B. (2009) Evolution and the concept of homology. In: Binder, M.D., Hirokawa, N., & Windhorst, U. (Eds.), Encyclopedic Reference of Neuroscience.Springer, New York, pp. 1208–1212.Google Scholar
Butler, A.B., & Hodos, W. (2005) Comparative Vertebrate Neuroanatomy, 2nd ed. John Wiley & Sons, Hoboken, NJ.Google Scholar
Butler, A.B., Reiner, A., & Karten, H.J. (2011) Evolution of the amniote pallium and the origins of mammalian neocortex. Ann NY Acad Sci 1225:14–27.CrossRefGoogle ScholarPubMed
Butler, A.B., & Saidel, W.M. (2000) Defining sameness: historical, biological, and generative homology. BioEssays 22:846–853.Google Scholar
Caballero-Bleda, M. (1988) Región alar del diencéfalo y mesencéfalo en el conejo : quimioarquitectonía de AChE y NADH-diaforasa como contribución a su neuroanatomíca comparada. PhD thesis, Universidad de Murcia.Google Scholar
Campbell, C.B.G., & Hodos, W. (1970) The concept of homology and the evolution of the nervous system. Brain Behav Evol 3:353–367.Google Scholar
Caretta, D., Sbriccoli, A., Santarelli, M., Pinto, F., Granato, A., & Minciacchi, D. (1996) Crossed thalamo-cortical and cortico-thalamic projections in adult mice. Neurosci Lett 204:69–72.Google Scholar
Chen, C.C., Winkler, C.M., Pfenning, A.R., & Jarvis, E.D. (2013) Molecular profiling of the developing avian telencephalon: regional timing and brain subdivision continuities. J Comp Neurol 521:3666–3701.Google Scholar
Clayton, N.S., Bussey, T.J., & Dickinson, A. (2003a) Can animals recall the past and plan for the future? Nat Rev Neurosci 4:685–691.Google Scholar
Clayton, N.S., Bussey, T.J., & Dickinson, A. (2003b) Prometheus to Proust: the case for behavioural criteria for “mental time travel.” Trends Cogn Sci 7:436–437.Google Scholar
Clayton, N.S., & Dickinson, A. (1998) Episodic-like memory during cache recovery by scrub jays. Nature 395:272–274.CrossRefGoogle ScholarPubMed
Clayton, N.S., & Dickinson, A. (1999) Scrub jays (Aphelocoma coerulescens) remember the relative time of caching as well as the location and content of their caches. J Comp Psychol 113:403–416.CrossRefGoogle ScholarPubMed
Clayton, N.S., Griffiths, D.P., Emery, N.J., & Dickinson, A. (2001) Elements of episodic-like memory in animals. Phil Trans Roy Soc Lond B 356:1483–1491.Google Scholar
Colombe, J.B., Sylvester, J., Block, J., & Ulinski, P.S. (2004) Subpial and stellate cells: two populations of interneurons in turtle visual cortex. J Comp Neurol 471:333–351.Google Scholar
Cordery, P., & Molnár, Z. (1999) Embryonic development of connections in turtle pallium. J Comp Neurol 413:26–54.3.0.CO;2-N>CrossRefGoogle ScholarPubMed
Crespo, C., Porteros, A., Arévalo, R., Briñón, J.G., Aijón, J., & Alonso, J. R. (1999) Distribution of parvalbumin immunoreactivity in the brain of the tench (Tinca tinca L., 1758). J Comp Neurol 413:549–571.Google Scholar
Csillag, A., & Montagnese, C.M. (2005) Thalamotelencephalic organization in birds. Brain Res Bull 66:303–310.Google Scholar
Dadda, M., Agrillo, C., Bisazza, A., & Brown, C. (2015) Laterality enhances numerical skills in the guppy, Poecilia reticulata. Front Behav Neurosci 9:285. doi:10.3389/fnbeh.2015.00285.Google Scholar
Dadda, M., Piffer, L., Agrillo, C., & Bisazza, A. (2009). Spontaneous number representation in mosquitofish. Cogn 122:343–348.Google Scholar
Darmaillacq, A.S., Dickel, L., Rahmani, N., & Shashar, N. (2011) Do reef fish, Variola louit and Scarus niger, perform amodal competition? Evidence from a field study. J Comp Psychol 125:273–277.Google Scholar
Dávila, J.C., Andreu, M.J., Real, A., Puelles, L., & Guirado, S. (2002) Mesencephalic and diencephalic afferent connections to the thalamic nucleus rotundus in the lizard, Psammodromus algirus. Europ J Neurosci 16:267–282.Google Scholar
Dávila, J.C., Guirado, S., & Puelles, L. (2000) Expression of calcium-binding proteins in the diencephalon of the lizard Psammodromus algirus. J Comp Neurol 427:67–92.Google Scholar
de Beer, G. (1971) Homology, an unsolved problem. In: Head, J.J., & Lowenstein, O.E. (Eds.), Oxford Biology Readers, No. 11. Oxford University Press, London.Google Scholar
Delius, J.D., & Bennetto, K. (1972) Cutaneous sensory projections to the avian forebrain. Brain Res 37:205–222.Google Scholar
Derman, C.R., & Barbas, H. (1994) Contralateral thalamic projections predominantly reach transitional cortices in rhesus monkey. J Comp Neurol 344:508–531.Google Scholar
Desfilis, E., Abellán, A., Sentandreu, V., & Medina, L. (2017) Expression of regulatory genes in the embryonic brain of a lizard and implications for understanding pallial organization and evolution. J Comp Neurol 526:166–202.Google Scholar
Desfilis, E., Font, E., Belekhova, M., & Kenigfest, N. (2002) Afferent and efferent projections of the dorsal anterior thalamic nuclei in the lizard Podarcis hispanica (Sauria, Lacertidae). Brain Res Bull 57:477–450.Google Scholar
Desfilis, E., Font, E., & Garcia-Verdugo, J.M. (1998) Trigeminal projections to the dorsal thalamus in a lacertid lizard, Podarcis hispanica. Brain Behav Evol 52:99–110.Google Scholar
Díaz, C., Yanes, C., Trujillo, C.M., & Puelles, L. (1994) The lacertidian reticular thalamic nucleus projects topographically upon the dorsal thalamus: experimental study in Gallotia galloti. J Comp Neurol 343:193–208.Google Scholar
Diekamp, B., Gagliardo, A., & Güntürkün, O. (2002a) Nonspatial and subdivision-specific working memory deficits after selective lesions of the avian prefrontal cortex. J Neurosci 22:9573–9580.Google Scholar
Diekamp, B., Kalt, T., & Güntürkün, O. (2002b) Working memory neurons in pigeons. J Neurosci 22:1–5.Google Scholar
Dinopoulos, A. (1994) Reciprocal connections of the motor neocortical area with the contralateral thalamus in the hedgehog (Erinaceus europaeus) brain. Europ J Neurosci 6:374–380.Google Scholar
Dirian, L., Galant, S., Coolen, M., Chen, W., Bedu, S., Houart, C., Bally-Cuif, L., & Foucher, I. (2014) Spatial regionalization and heterochrony in the formation of adult pallial neural stem cells. Dev Cell 30:123–136.Google Scholar
Ditz, H.M., & Nieder, A. (2016) Sensory and working memory representations of small and large numerosities in the crow forebrain. J Neurosci 36:12044–12052.Google Scholar
Doron, N.N., & LeDoux, J.E. (2000) Cells in the posterior thalamus project to both amygdala and temporal cortex: a quantitative retrograde double-labeling study in the rat. J Comp Neurol 425:257–274.Google Scholar
Dugas-Ford, J., & Ragsdale, C.W. (2015) Levels of homology and the problem of neocortex. Annu Rev Neurosci 38:351–368.Google Scholar
Dugas-Ford, J., Rowell, J.J., & Ragsdale, C.W. (2012) Cell-type homologies and the origins of neocortex. Proc Nat’l Acad Sci 109:16974–16979.Google Scholar
Durán, E., Ocaña, F.M., Broglio, C., Rodríguez, F., & Salas, C. (2010) Lateral but not medial telencephalic pallium ablation impairs the use of goldfish spatial allocentric strategies in a “hole-board” task. Behav Brain Res 214:480–487.Google Scholar
Ebbesson, S.O.E. (1980) The parcellation theory and its relation to interspecific variability in brain organization, evolutionary and ontogenetic development and neuronal plasticity. Cell Tiss Res 213:179–212, doi:10.1007/BF00234781.Google Scholar
Ebbesson, S.O.E. (1984) An update of the parcellation theory. Behav Brain Sci 7:350–366, doi:10.1017/S0140525X00018628.Google Scholar
Ebbesson, S.O.E. (2020) How the parcellation theory of comparative forebrain specialization emerged from the Division of Neuropsychiatry at the Walter Reed Army Institute of Research. J Hist Neurosci 30:24–55, doi:10.1080/0964704X.2020.1763759.Google Scholar
Emery, N.J., & Clayton, N.S. (2016) An avian perspective on stimulating other minds Learn Behav 44:203–204.Google Scholar
Endepols, H., Roden, K., Luksch, H., Dicke, U., & Walkowiak, W. (2004) Dorsal striatopallidal system in anurans. J Comp Neurol 468:299–310.Google Scholar
Evans, S.E. (2000) Amniote evolution. In: Bock, G.R., & Cardew, G. (Eds.), Evolutionary Developmental Biology of the Cerebral Cortex (Novartis Foundation Symposium 228). John Wiley & Sons, Ltd., Chichester, pp. 109–113.Google Scholar
Fernández, M., Ahumada-Galleguillos, P., Marían, G., & Mpodozis, J. (2019) Intratelencephalic projections of the avian visual dorsal ventricular ridge: laminarly segregated, reciprocally and topographically organized. J Comp Neurol 413:26–54.Google Scholar
Folgueira, M., Bayley, P., Navratilova, P., Becker, T.S., Wilson, S.W., & Clarke, J.D.W. (2012) Morphogenesis underlying the development of the everted teleost telencephalon. Neural Dev 7:32.Google Scholar
García-Moreno, F., & Molnár, Z. (2020) Variations of telencephalic development that paved the way for neocortical evolution. Progr Neurobiol 194:101865, doi:10.1016/j.pneurobio.2020.101865.Google Scholar
Gilbert, S.R. (1994) Developmental Biology, 4th ed. Sinauer Associates, Inc., Sunderland MA.Google Scholar
Gómez-Laplaza, L.M., & Gerlai, R. (2020) Food density and preferred quantity: discrimination of small and large numbers in angelfish (Pterophyllum scalare). Sci Rep 9:15305. doi:10.1007/s10071-0C20-01355-6.CrossRefGoogle Scholar
González, G., Puelles, L., & Medina, L. (2002). Organization of the mouse dorsal thalamus based on topology, calretinin immunostaining, and gene expression. Brain Res Bull 57:439–442.Google Scholar
González, M.J., Yáñez, J., and Anadón, R. (1999) Afferent and efferent connections of the torus semicircularis in the sea lamprey: an experimental study. Brain Res 826:83–94.Google Scholar
Griffiths, D., Dickinson, A., & Clayton, N. (1999) Episodic memory: what can animals remember about their past? Trends Cogn Sci 3:74–80.CrossRefGoogle ScholarPubMed
Grosenick, L., Clement, T.S., & Fernald, R.D. (2007) Fish can infer social rank by observation alone. Nature 445:429–432.CrossRefGoogle ScholarPubMed
Gruber, R., Schiesti, M., Boeckle, M., Frohnwieser, A., Miller, R., Gray, R.D., Clayton, N.S., & Taylor, A.H. (2019) New Caledonian crows use mental representations to solve metatool problems. Curr Biol 29:686–692.CrossRefGoogle ScholarPubMed
Guillén, M. (1991) Estructura del epitálamo y complejo superior del talámo dorsal en aves: studio embryológico. Posibles homologies con mamíferos. PhD thesis, Universidad de Murcia.Google Scholar
Halassa, M.M., & Sherman, S.M. (2019) Thalamocortical circuit motifs: a general framework. Neuron 103:762–770.Google Scholar
Hall, J.A., Foster, R.E., Ebner, F.F., & Hall, W.C. (1977) Visual cortex in a reptile, the turtle (Pseudemys scripta and Chrysemys picta). Brain Res 130:197–216.Google Scholar
Harting, J.K., Hall, W.C., & Diamond, I.T. (1972) Evolution of the pulvinar. Brain Behav Evol 6:424–452.Google Scholar
Harting, J.K., Updyke, B.V., & van Lieshout, D.P. (2001) Striatal projections from the cat visual thalamus. Europ J Neurosci 14:893–896.Google Scholar
Henderson, J., Hurly, T.A., Bateson, M., & Healy, S.D. (2006) Timing in free-living rufous hummingbirds, Selasphorus rufus. Curr Biol 16:512–515.Google Scholar
Herculano-Houzel, S. (2020) Birds do have a brain cortex—and think. Sci 369:1567–1568.Google Scholar
Herkenham, M. (1978) The connections of the nucleus reuniens thalami: evidence for a direct thalamo-hippocampal pathway in the rat. J Comp Neurol 177:589–610.Google Scholar
Herrick, J.L., & Keifer, J. (1997) A hypothalamic projection to the turtle red nucleus: An anterograde and retrograde tracing study. Exp Brain Res 116:556–560.Google Scholar
Hodos, W., & Campbell, C.B.G. (1969) Scala naturae: why there is no theory in comparative psychology. Psychol Rev 76:337–350.Google Scholar
Hofmann, M.H., & Northcutt, R.G. (2012) Forebrain organization in elasmobranchs. Brain Behav Evol 80:142–151.Google Scholar
Hollis, D.M., & Boyd, S.K. (2005) Distribution of GABA-like immunoreactive cell bodies in the brains of two amphibians, Rana catesbeiana and Xenopus laevis. Brain Behav Evol 65:127–142.CrossRefGoogle ScholarPubMed
Hoogland, P.V. (1977) Efferent connections of the striatum in Tupinambis nigropunctatus. J Morphol 152:229–246.Google Scholar
Hoogland, P.V., & Vermeulen-Van der Zee, (1989) Efferent connections of the dorsal cortex of the lizard Gekko gecko studied with Phaseolus vulgaris-leucoagglutinin. J Comp Neurol 285:289–303.Google Scholar
Hotta, T., Ueno, K., Hataji, Y., Kuroshima, H., Fujita, K., & Kohda, M. (2020) Transitive inference in cleaner wrasses (Labroides dimidiatus). PLoSONE 15(8): e0237817. doi:10.1371/journal.pone.0237817.Google Scholar
Hu, J., & Wang, S.-R. (2001) Firing patterns and morphological features of neurons in the pigeon nucleus rotundus. Brain Behav Evol 57:343–348.Google Scholar
Husband, S., & Shimizu, T. (1999) Efferent projections of the ectostriatum in the pigeon (Columba livia). J Comp Neurol 406:329–345.Google Scholar
Iwaniuk, A.N. (2017) The evolution of cognitive brains in non-mammals. In: Watanabe, S., Hofman, M.A., & Shimizu, T. (Eds.), Evolution of the Brain, Cognition, and Emotion in Vertebrates. Springer Japan KK, Tokyo, pp. 101–124.Google Scholar
Jarvis, E.D., Yu, J., Rivas, M.V., Horita, H., Feenders, G., Whitney, O., Jarvis, S.C., Jarvis, E.R., Kubikova, L., Puck, A.E.P., Siang-Bakshi, C., Martin, S., McElroy, M., Hara, E., Howard, J., Pfenning, A., Mouritsen, H., Chen, C.-C., & Wada, K. (2013) Global view of the functional molecular organization of the avian cerebrum: mirror images and functional columns. J Comp Neurol 521:3614–3665.Google Scholar
Jiao, Y., Medina, L., Veenman, L.C., Toledo, C., Puelles, L., & Reiner, A. (2000) Identification of the anterior nucleus of the ansa lenticularis in birds as the homologue of the mammalian subthalamic nucleus. J Neurosci 20:6998–7010.Google Scholar
Kaas, J.H. (2017a) Evolution of the visual cortex in primates. In: Kaas, J.H., & Krubitzer, L. (Eds.), Evolution of Nervous Systems. Vol. 3: The Nervous Systems of Non-human Primates, 2nd ed. Elsevier, Amsterdam, pp. 187–201.Google Scholar
Kaas, J.H. (2017b) The organization of neocortex in early mammals. In: Kaas, J.H., & Herculano-Houzel, S. (Eds.), Evolution of Nervous Systems. Vol. 2: The Nervous Systems of Early Mammals and Their Evolution, 2nd ed.Elsevier, Amsterdam, pp. 87–101.Google Scholar
Karten, H.J. (1968) The ascending auditory pathways in the pigeon (Columba livia): II. Telencephalic projections of the nucleus ovoidalis thalami. Brain Res 11:134–153.Google Scholar
Karten, H.J. (1969) The organization of the avian telencephalon and some speculations on the phylogeny of the amniote telencephalon. Ann NY Acad Sci 167:164–179.Google Scholar
Karten, H.J., Cox, K., & Mpodozis, J. (1997) Two distinct populations of tectal neurons have unique connections within the retinotectorotundal pathway of the pigeon (Columba livia). J Comp Neurol 387: 449–465.Google Scholar
Karten, H.J., & Hodos, W. (1970) Telencephalic projections of the nucleus rotundus in the pigeon (Columba livia). J Comp Neurol 140:35–52.Google Scholar
Karten, H.J., Hodos, W., Nauta, W.H.J., & Revzin, A. (1973) Neural connections of the “visual Wulst” of the avian telencephalon: experimental studies in the pigeon (Columba livia) and owl (Speotyto cunicularia). J Comp Neurol 150:253–278.Google Scholar
Karten, H.J., Konishi, M., & Pettigrew, J.D. (1978) Somatosensory representation in the anterior Wulst of the owl Speotyto cunicularis. Soc Neurosci Abstr 4:554.Google Scholar
Keifer, J., & Lustig, D.G. (2000) Comparison of cortically and subcortically controlled motor systems. II. Distribution of anterogradely labeled terminal boutons on intracellularly filled rubrospinal neurons. J Comp Neurol 416:101–111.Google Scholar
Kemp, T.S. (2005) The Origin and Evolution of Mammals. Oxford University Press, Oxford, UK.Google Scholar
Kenigfest, N., Belekhova, M., Repérant, J., Rio, J.-P., Ward, R., & Vesselkin, N. (2005) The turtle thalamic anterior entopeduncular nucleus shares connectional and neurochemical characteristics with the mammalian thalamic reticular nucleus. J Chem Neuroanat 30:129–143.Google Scholar
Kenigfest, N., Repérant, J., Belekhova, M., Rio, J.-P., & Ward, R. (2007) Evolution of the visual tectogeniculate and pretectogeniculate pathways in the brain of amniote vertebrates. In: Kaas, J.H., & Bullock, T.H. (Eds.), Evolution of Nervous Systems: A Comprehensive Reference. Vol. 2, Nonmammalian Vertebrates. Elsevier, Amsterdam, pp. 459–467.Google Scholar
Kirsch, J.A., Güntürkün, O., & Rose, J. (2008) Insight without cortex: lessons from the avian brain. Consc Cogn 17:475–483.Google Scholar
Kohda, M., Hotta, T., Takeyama, T., Awata, S., Tanaka, H., Asai, J., & Jordan, A.L. (2019) If a fish can pass the mark test, what are the implications for consciousness and self-awareness testing in animals? PLoS Biol 17: e3000021. doi:10.1371/journal.pbio.3000021.Google Scholar
Krubitzer, L., & Seelke, A.M.H. (2012) Cortical evolution in mammals: the bane and beauty of phenotypic variability. Proc Nat Acad Sci USA 109, Suppl. 1:10647–10654.Google Scholar
Krusche, P., Uller, C., & Dicke, U. (2010) Quantity discrimination in salamanders. J Exp Biol 213:1822–1828.Google Scholar
Kudo, M., Glendenning, K.K., Frost, S.B., & Masterton, R.B. (1986) Origin of mammalian thalamocortical projections. I. Telencephalic projections of the medial geniculate body in the opossum (Didelphis virginiana). J Comp Neurol 245:176–197.Google Scholar
Laberge, F., Mühlenbrock-Lenter, S., Dicke, U., & Roth, G. (2008) Thalamo-telencephalic pathways in the fire-bellied toad Bombina orientalis. J Comp Neurol 508:806–823.Google Scholar
Lichtneckert, R., & Reichert, H. (2005) Insights into the urbilaterian brain: conserved genetic patterning mechanisms in insect and vertebrate brain development. Heredity 94:465–477.Google Scholar
Liem, K.F., Bemis, W.E., Walker, W.F., Jr., & Grande, L. (2001) Functional Anatomy of the Vertebrates: An Evolutionary Perspective. Harcourt College Publishers, Fort Worth.Google Scholar
Llinás, R., & Paré, D. (1991) Coherent oscillations in specific and nonspecific thalamocortical networks and their role in cognition. In Steriade, M., Jones, E.G., & McCormick, D.A. (Eds.), Thalamus. Vol. II: Experimental and Clinical Aspects. Elsevier, Amsterdam, pp. 501–516.Google Scholar
Llinás, R., Ribary, U., Contreras, D., & Pedroarena, C. (1998) The neuronal basis for consciousness. Phil Trans Roy Soc Lond 353:1841–1849.Google Scholar
Llinás, R.R., & Steriade, M. (2006) Bursting of thalamic neurons and states of vigilance. J Neurophysiol 95:3297–3308.Google Scholar
Llinás, R.R., Urbano, F.J., Leznik, E., Ramírez, R.R., & van Marle, H.J.F. (2005) Rhythmic and dysrhythmic thalamocortical dynamics: GABA systems and the edge effect. Trends Neurosci 28:325–333.Google Scholar
Lohman, A.H.M., & Van Woerden-Verkley, (1978) Ascending connections to the forebrain in the tegu lizard. J Comp Neurol 182:555–594.Google Scholar
López, J.M., Morona, R., Moreno, N., & González, A. (2017) The organization of the central nervous system of lungfishes: an immunohistochemical approach. In: Kaas, J.H., & Striedter, G. (Eds.), Evolution of Nervous Systems. Vol. 1: The Evolution of the Nervous Systems in Nonmammalian Vertebrates, 2nd ed. Elsevier, Amsterdam, pp. 121–139.Google Scholar
López-Bendito, G., Flames, N., Ma, L., Fouquet, C., Di Medlio, A., Tessier-Lavigne, M., & Marín, O. (2007) Robo1 and Robo2 cooperate to control the guidance of major axonal tracts in the mammalian forebrain. J Neurosci 27:3395–3407.Google Scholar
López-Bendito, G., & Molnár, Z. (2003) Thalamocortical development: how are we going to get there? Nat Rev Neurosci 4:276–289.Google Scholar
Luksch, H., Cox, K., & Karten, H.J. (1998) Bottlebrush dendritic endings and large dendritic fields: motion-detecting neurons in the tectofugal pathway. J Comp Neurol 396:399–414.Google Scholar
Lynn, A.M., Schneider, D.A., & Bruce, L.L. (2015) Development of the avian dorsal thalamus: patterns and gradients of neurogenesis. Brain Behav Evol 86:94–109.Google Scholar
Macchi, G., Bentivoglio, M., Minciacchi, D., & Molinari, M. (1996) Trends in the anatomical organization and functional significance of the mammalian thalamus. Ital J Neurol Sci 17:105–129.Google Scholar
Mancilla, J.G., & Ulinski, P.S. (2001) Role of GABA(A)-mediated inhibition in controlling the responses of regular spiking cells in turtle visual cortex. Vis Neurosci 18:9–24.Google Scholar
Manrod, J.D., Hartdegen, R., & Burghardt, G.M. (2008) Rapid solving of a problem apparatus by juvenile black-throated monitor lizards (Varanus albigularis albigularis). Anim Cogn 11:267–273.Google Scholar
Martínez-de-la-Torre, M. (1985) Estructura del mesencéfalo y diencéfalo en aves y reptiles: aportaciones a una síntesis en la búsqueda de homologías. PhD thesis, Universidad de Murcia.Google Scholar
Martínez-de-la-Torre, M., Pombol, M.A., & Puelles, L., (2011) Distal-less-like protein distribution in the larval lamprey forebrain. Neurosci 178:270–284.Google Scholar
Martínez-García, F., Martínez-Marcos, A., & Lanuza, E. (2002) The pallial amygdala of amniote vertebrates: evolution of the concept, evolution of the structure. Brain Res Bull 57:463–4Google Scholar
Martínez-García, F., Novejarque, A., & Lanuza, E. (2007) Evolution of the amygdala in vertebrates. In: Kaas, J.H., & Bullock, T.H. (Eds.), Evolution of Nervous Systems: A Comprehensive Reference. Vol. 2, Nonmammalian Vertebrates. Elsevier, Amsterdam, pp. 255–334.Google Scholar
Medina, L., & Abellán, A. (2009) Development and evolution of the pallium. Sem Cell Devel Biol 20:698–711.Google Scholar
Medina, L., Abellán, A., Vicario, A., Castro-Robles, B., & Desfilis, E. (2017) The amygdala. In: Kaas, J.H., & Striedter, G. (Eds.), Evolution of Nervous Systems. Vol. 1: The Evolution of the Nervous Systems in Nonmammalian Vertebrates, 2nd ed.Elsevier, Amsterdam, pp. 427–478.Google Scholar
Medina, L., Veenman, C.L., & Reiner, A. (1997). Evidence for a possible avian dorsal thalamic region comparable to the mammalian ventral anterior, ventral lateral, and oral ventroposterolateral nuclei. J Comp Neurol 384:86–108.Google Scholar
Médina, M., Repérant, J., Dufour, S., Ward, R., Le Belle, N., & Miceli, D. (1994) The distribution of GABA-immunoreactive neurons in the brain of the silver eel (Anguilla anguilla L.). Anat Embryol 189:25–39.Google Scholar
Meléndez-Ferro, M., Pérez-Costas, E., Villar-Cheda, , Abalo, X.M., Rodriguez-Muñoz, R., Rodicio, M.C., & Anadón, R. (2002) Ontogeny of γ-aminobutyric acid-immunoreactive neuronal populations in the forebrain and midbrain of the sea lamprey. J Comp Neurol 446:360–376.Google Scholar
Molnár, Z., Garel, S., López-Bendito, G., Maness, P., & Price, D.J. (2012) Mechanisms controlling the guidance of thalamocortical axons through the embryonic forebrain. Europ J Neurosci 35:1573–1585.Google Scholar
Montagnese, C.M., Mezey, S.E., & Csillag, A. (2003) Efferent connections of the dorsomedial thalamic nuclei of the domestic chick (Gallus domesticus). J Comp Neurol 459:301–326.CrossRefGoogle ScholarPubMed
Montiel, J.F., & Aboitiz, F. (2015) Pallial patterning and the origin of the isocortex. Front Neurosci 9. doi: 10.3389/fnins.2015.00377.Google Scholar
Moreno, N., Bachy, I., Rétaux, S., & González, A. (2004) LIM-homeodomain genes as developmental and adult genetic markers of Xenopus forebrain functional subdivisions. J Comp Neurol 472:52–72.Google Scholar
Moreno, N., Morona, R., López, J.M., and González, A. (2017) The diencephalon and hypothalamus of nonmammalian vertebrates: evolutionary and developmental traits. In: Kaas, J.H., & Striedter, G. (Eds.), Evolution of Nervous Systems. Vol. 1: The Evolution of the Nervous Systems in Nonmammalian Vertebrates, 2nd ed.Elsevier, Amsterdam, pp. 409–426.Google Scholar
Morrow, J., Mosher, C., & Gothard, K. (2019) Multisensory neurons in the primate amygdala. J Neurosci 39:3663–3675.Google Scholar
Mpodozis, J., Cox, K., Shimizu, T., Bischoff, H.J., Woodson, W., & Karten, H.J. (1996) GABAergic inputs to the nucleus rotundus (pulvinar inferior) of the pigeon (Columba livia). J Comp Neurol 374:204–222.Google Scholar
Nakagawa, Y., & O’Leary, D.D.M. (2001) Combinatorial expression patterns of LIM-homeodomain and other regulatory genes parcellate developing thalamus. J Neurosci 21:2711–2725.Google Scholar
Nieder, A., Wagener, L., & Rinnert, P. (2020) A neural correlate of sensory consciousness in a corvid bird. Sci 369:1626–1629.Google Scholar
*Nieuwenhuys, R., ten Donkelaar, H.J., & Nicholson, C. (1998) The Central Nervous System of Vertebrates, Vol. 1. Springer-Verlag, Berlin.CrossRefGoogle Scholar
*Nieuwenhuys, R., ten Donkelaar, H.J., & Nicholson, C. (1998) The Central Nervous System of Vertebrates. Springer-Verlag, Berlin.Google Scholar
Nomura, T., & Hirata, T. (2017) The neocortical homologues in nonmammalian amniotes: bridging the hierarchical concepts of homology through comparative neurogenesis. In: Kaas, J.H., & Herculano-Houzel, S. (Eds.), Evolution of Nervous Systems. Vol. 2: The Nervous Systems of Early Mammals and Their Evolution, 2nd ed.Elsevier, Amsterdam, pp. 195–204.Google Scholar
Northcutt, R.G. (1977) Retinofugal projections in the lepidosirenid lungfishes. J Comp Neurol 174:553–574.Google Scholar
Northcutt, R.G. (1980) Retinal projections in the Australian lungfish. Brain Res 185:85–90.Google Scholar
Northcutt, R.G. (1984) Evolution of the vertebrate central nervous system: patterns and processes. Amer Zool 24:701–716.Google Scholar
Northcutt, R.G. (1985) Central nervous system phylogeny: evaluation of hypotheses. Fortsch Zool 30:497–505.Google Scholar
Northcutt, R.G. (1989) Brain variation and phylogenetic trends in elasmobranch fishes. J Exp Zool Suppl 2:83–100.Google Scholar
Northcutt, R.G. (2003) The use and abuse of developmental data. Behav Brain Sci 26:565–566.Google Scholar
Northcutt, R.G. (2006) Connections of the lateral and medial divisions of the goldfish telencephalic pallium. J Comp Neurol 494:903–943.Google Scholar
Northcutt, R.G. (2009) Telencephalic organization in the spotted African lungfish, Protopterus dolloi: a new cytological model. Brain Behav Evol 73:59–80.Google Scholar
Northcutt, R.G. (2013) Variations in reptilian brains and cognition. Brain Behav Evol 82:45–54.Google Scholar
Northcutt, R.G., & Wicht, H. (1997) Afferent and efferent connections of the lateral and medial pallia of the silver lamprey. Brain Behav Evol 49:1–19.Google Scholar
Novejarque, A., Lanuza, E., & Martínez-Garcia, F. (2004) Amygdalostriatal projections in reptiles: a tract-tracing study in the lizard Podarcis hispanica. J Comp Neurol 479:287–308.Google Scholar
Okano, H., & Temple, S. (2009) Cell types to order: temporal specification of CNS stem cells. Curr Opin Neurobiol 19:112–119.Google Scholar
Olkowicz, S., Kocourek, M., Lučan, R.K., Porteš, M., Fitch, W.T., Herculano-Houzel, S., & Němec, P. (2016) Birds have primate-like numbers of neurons in the forebrain. Proc Nat Acad Sci USA 113:7255–7260.Google Scholar
Panchen, A.L. (1999) Homology—history of a concept. In: Bock, G.R., & Cardew, G. (Eds.), Homology: Novartis Foundation Symposium 222. John Wiley & Sons, Chichester.Google Scholar
Pasko, L., (2010) Tool-like behavior in the sixbar wrasse, Thalassoma hardwicke (Bennett, 1830). Zool Biol 29:767–773.Google Scholar
Patton, B.W., & Braithwaite, V.A. (2015) Changing tides: ecological and historical perspectives on fish cognition. WIREs Cogn Sci 6:159–176. doi:10.1002/wcs.1337.Google Scholar
Paz-y-Miño, G., Bond, A.B., Kamil, A.C., & Balda, R.P. (2004) Pinyon jays use transitive inference to predict social dominance. Nature 430:778–781.Google Scholar
Peake, T.M., Terry, A.M.R., McGregor, P.K., & Dabelsteen, T. (2001) Male great tits eavesdrop on simulated male-to-male vocal interactions. Proc Roy Soc Lond B 268:1183–1187.Google Scholar
Peake, T.M., Terry, A.M.R., McGregor, P.K., & Dabelsteen, T. (2002) Do great tits assess rivals by combining direct experience with information gathered by eavesdropping? Proc Roy Acad Lond B 269:1925–1929.Google Scholar
Pepperberg, I.M. (1999) The Alex Studies: Cognitive and Communicative Abilities of Grey Parrots. Harvard University Press, Cambridge, MA.Google Scholar
Pepperberg, I.M. (2006) Grey parrot (Psittacus erithacus) numerical abilities: addition and further experiments on a zero-like concept. J Comp Psychol 120:1–11.Google Scholar
Pepperberg, I.M. (2013) Abstract concepts: data from a grey parrot. Behav Proc 93:82–90.Google Scholar
Pepperberg, I.M. (2020) The comparative psychology of intelligence: some thirty years later. Front Psychol 11. doi:10.3389/fpsyg.2020.00973.Google Scholar
Pepperberg, I.M., & Nakayama, K. (2016) Robust representation of shape in a grey parrot (Psittacus erithacus). Cogn 153:146–160.Google Scholar
Polenova, O.A., & Vesselkin, N.P. (1993) Olfactory and nonolfactory projections in the river lamprey (Lampetra fluviatilis) telencephalon. J Hirnforsch 34:261–279.Google Scholar
Pombal, M.A., & Megías, M. (2017) The nervous system of jawless vertebrates. In: Kaas, J.H., & Striedter, G. (Eds.), Evolution of Nervous Systems. Vol. 1: The Evolution of the Nervous Systems in Nonmammalian Vertebrates, 2nd ed. Elsevier, Amsterdam, pp. 37–57.Google Scholar
Pombal, M.A., Megías, M., Bardet, S.M., & Puelles, L. (2009) New and old thoughts on the segmental organization of the forebrain in lampreys. Brain Behav Evol 74:7–19.Google Scholar
Portavella, M., Torres, B., & Salas, C. (2004) Avoidance response in goldfish: emotional and temporal involvement of medial and lateral telencephalic pallium. J Neurosci 24:2335–2342.Google Scholar
Powers, A.S., & Reiner, A. (1980) A stereotaxic atlas of the forebrain and midbrain of the Eastern painted turtle (Chrysemys picta picta). J Hirnforsch 21:125–159.Google Scholar
Preuss, T.M., & Goldman-Rakic, P.S. (1987) Crossed corticothalamic and thalamocortical connections of macaque prefrontal cortex. J Comp Neurol 257:269–281.Google Scholar
Pritz, M.B. (1995) The thalamus of reptiles and mammals: similarities and differences. Brain Behav Evol 46:197–208.Google Scholar
Pritz, M.B. (2015) Crocodilian forebrain: evolution and development. Integrative Comp Biol 55:949–961.Google Scholar
Pritz, M.B., & Stritzel, M.E. (1988) Thalamic nuclei that project to reptilian telencephalon lack GABA and GAD immunoreactive neurons and puncta. Brain Res 457:154–159.Google Scholar
Pritz, M.B., & Stritzel, M.E. (1990) A different type of vertebrate thalamic organization. Brain Res 525:330–334.Google Scholar
Pritz, M.B., & Stritzel, M.E. (1994) Glutamic acid decarboxylase immunoreactivity in some dorsal thalamic nuclei in Crocodilia. Neurosci Lett 165:109–112.Google Scholar
Puelles, L., (2011) Pallio-pallial tangential migrations and growth signaling: new scenario for cortical evolution? Brain Behav Evol 78:108–127.Google Scholar
Puelles, L., Amat, J.A., & Martínez-de-la-Torre, M. (1987) Segment-related, mosaic neurogenetic pattern in the forebrain and mesencephalon of early chick embryos: I. Topography of AChE-positive neuroblasts up to stage HH18. J Comp Neurol 266: 247–268.Google Scholar
Puelles, L., Ayad, A., Alonso, A., Sandoval, J.E., Martínez-de-la-Torre, M., Medina, L., & Ferran, J.L. (2016) Selective early expression of the orphan nuclear receptor Nr4a2 identifies the claustrum homolog in the avian mesopallium: impact on sauropsidian/mammalian pallium comparisons. J Comp Neurol 524:665–703.Google Scholar
Puelles, L., Kuwana, E., Puelles, E., Bulfone, A., Shimamura, K., Keleher, J., Smiga, S., & Rubenstein, J.L. (2000) Pallial and subpallial derivatives of the embryonic chick and mouse telencephalon, traced by the expression of genes Dlx-2, Emx-1, Nkx-2.1, Pax-6, and TBR-1. J Comp Neurol 424:409–438.Google Scholar
Puelles, L., & Medina, L. (2002) Field homology as a way to reconcile genetic and developmental variability with adult homology. Brain Res Bull 57:243–255.Google Scholar
Puelles, L., Medina, L., Borello, U., Legaz, I., Teissier, A., Pierani, A., & Rubenstein, J.L.R. (2015) Radial derivatives of the mouse ventral pallium traced with Dbx1-LacZ reporters. J Chem Neuroanat 75:2–19.Google Scholar
Puelles, L., Milán, F.J., & Martínez-de-la-Torre, M. (1996) A segmental map of architectonic subdivisions in the diencephalon of the frog Rana perezi: acetylcholinesterase-histochemical observations. Brain Behav Evol 47:279–310.Google Scholar
Puelles, L., Sandoval, J.E., Ayad, A., del Corral, R., Alonso, A., Ferran, J.L., & Martínez-de-la-Torre, (2017) The pallium in reptiles and birds in the light of the updated tetrapartite pallium model. In: Kaas, J.H., & Striedter, G. (Eds.), Evolution of Nervous Systems. Vol. 1: The Evolution of the Nervous Systems in Nonmammalian Vertebrates, 2nd ed.Elsevier, Amsterdam, pp. 519–555.Google Scholar
Raff, R.A. (1996) The Shape of Life: Genes, Development, and the Evolution of Animal Form. University of Chicago Press, Chicago.Google Scholar
Raghanti, M.A., Munger, E.L., Wicinski, B., Butti, C., & Hof, P.R. (2017) Comparative structure of the cerebral cortex in large mammals. In: Kaas, J.H., & Herculano-Houzel, S. (Eds.), Evolution of Nervous Systems. Vol. 2: The Nervous Systems of Early Mammals and Their Evolution, 2nd ed. Elsevier, Amsterdam, pp. 267–289.Google Scholar
Redies, C., Ast, M., Nakagawa, S., Takeichi, M., Martínez-de-la-Torre, M., & Puelles, L. (2000) Morphogenetic fate of diencephalic prosomeres and their subdivisions revealed by mapping cadherin expression. J Comp Neurol 421:481–514.Google Scholar
Reiner, A. (1993) Neurotransmitter organization and connections of turtle cortex: implications for the evolution of mammalian isocortex. Comp Biochem Physiol A 104:735–748.Google Scholar
Reiner, A. (2002) Functional circuitry of the avian basal ganglia: implications for basal ganglia organization in stem amniotes. Brain Res Bull 57:513–528.Google Scholar
Reiner, A. (2012) You are who you talk with—a commentary on Dugas-Ford et al. PNAS, 2012. Brain Behav Evol 81:146–149 doi:10.1159/000348281.Google Scholar
Reiner, A., Medina, L., & Veenman, L.C. (1998) Structural and functional evolution of the basal ganglia in vertebrates. Brain Res Rev 28:235–285.Google Scholar
Reiner, A., Perkel, D.J., Bruce, L.L., Butler, A.B., Csillag, A., Kuenzel, W., Medina, L., Paxinos, G., Shimizu, T., Striedter, G., Wild, M., Ball, G.F., Durand, S., Güntürkün, O., Lee, D.W., Mello, C.V., Powers, A., White, S.A., Hough, G., Kubikova, L., Smulders, T.V., Wada, K., Dugas-Ford, J., Husband, S., Yamamoto, K., Yu, J., Siang, C., & Jarvis, E.D. (2004) Avian Brain Nomenclature Forum. Revised nomenclature for avian telencephalon and some related brainstem nuclei.J Comp Neurol 473:377–414.Google Scholar
Reiner, A., Yamamoto, K., & Karten, H.J. (2005) Organization and evolution of the avian forebrain. Anat Rec 287A:1080–1102.Google Scholar
Reisz, R.R. (1997) The origin and early evolutionary history of amniotes. Trends Ecol Evol 12:218–222.Google Scholar
Rikhye, R.V., Wimmer, R.D., & Halassa, M.M. (2018) Toward an integrative theory of thalamic function. Annu Rev Neurosci 41:163–183. doi:10.1146/annurev-neuro-080317-062144.Google Scholar
Rink, E., & Wullimann, M.F. (2004) Connections of the ventral telencephalon (subpallium) in the zebrafish (Danio rerio). Brain Res 1011:206–220.Google Scholar
Rinnert, P., Kirschhock, M.E., & Nieder, A. (2019) Neuronal correlates of spatial working memory in the endbrain of crows. Curr Biol 29:2616–2624.Google Scholar
Rio, J.-P., Repérant, J., Ward, R., Miceli, D., & Medina, M. (1992) Evidence of GABA-immunopositive neurons in the dorsal part of the lateral geniculate nucleus of reptiles: morphological correlates with interneurons. Neurosci 47:395–407.Google Scholar
Rodríguez, F., López, J.C., Vargas, J.P., Broglio, C., Gómez, Y., & Salas, C. (2002) Spatial memory and hippocampal pallium through vertebrate evolution: insights from reptiles and teleost fish. Brain Res Bull 57:499–503.Google Scholar
Rodríguez-Moldes, I., Santos-Durán, G.N., Pose-Méndez, S., Quintana-Urzainqui, I., & Candal, E. (2017) The brains of cartilaginous fishes. In: Kaas, J.H., & Striedter, G. (Eds.), Evolution of Nervous Systems. Vol. 1: The Evolution of the Nervous Systems in Nonmammalian Vertebrates, 2nd ed.Elsevier, Amsterdam, pp. 77–97.Google Scholar
Rose, J.E. (1942) The ontogenetic development of the rabbit’s diencephalon. J Comp Neurol 77:61–129.Google Scholar
Roth, G., Grunwald, W., & Dicke, U. (2003) Morphology, axonal projection pattern, and responses to optic nerve stimulation of thalamic neurons in the fire-bellied toad Bombina orientalis. J Comp Neurol 461:91–110.Google Scholar
Roth, G., Laberge, F., Mühlenbrock-Lenter, S., & Grunwald, W. (2007) Organization of the pallium in the fire-bellied toad Bombina orientalis. I: morphology and axonal projection pattern of neurons revealed by intracellular biocytin labeling. J Comp Neurol 501:443–464.Google Scholar
Roth, T.C. II, Krochmal, A.R., & LaDage, L.D. (2019) Reptilian cognition: a more complex picture via integration of neurological mechanisms, behavioral constraints, and evolutionary context. BioEssays 41. doi:10.1002/bies.201900033.Google Scholar
Rowe, T.B. (2017) The emergence of mammals. In: Kaas, J.H., & Herculano-Houzel, S. (Eds.), Evolution of Nervous Systems. Vol. 2: The Nervous Systems of Early Mammals and Their Evolution, 2nd ed.Elsevier, Amsterdam, pp. 1–52.Google Scholar
Sherman, S.M., & Guillery, R.W. (2013) Functional Connections of Cortical Areas: A New View from the Thalamus. MIT Press, Cambridge, MA.Google Scholar
Shi, W., Xianyu, A., Han, Z., Tang, X., Li, Z., Zhong, H., Mao, T., Huang, K., & Shi, S.-H. (2017) Ontogenetic establishment of order-specific nuclear organization in the mammalian thalamus. Nat Neurosci 20:516–528.Google Scholar
Simpson, G.G. (1961) Principles of Animal Taxonomy. Columbia University Press, New York.Google Scholar
Smith-Fernandez, A., Pieau, C., Repérant, J., Boncinelli, E., & Wassef, M. (1998) Expression of the Emx-1 and Dlx-1 homeobox genes define three molecularly distinct domains in the telencephalon of mouse, chick, turtle and frog embryos: implications for the evolution of telencephalic subdivisions in amniotes. Devel 2111:2099–2111.Google Scholar
Sovrano, V.A., & Bisazza, A. (2008) Recognition of partly occluded objects by fish. Anim Cogn 11:161–166.Google Scholar
Sovrano, V.A., & Bisazza, A. (2009) Perception of subjective contours in fish. Percep 38:579–590.Google Scholar
Stacho, M., Herold, C., Rook, N., Wagner, H., Axer, M., Amunts, K., & Gunturkun, O. (2020) A cortex-like canonical circuit in the avian forebrain. Sci 369:eabc5534.Google Scholar
Stancher, G., Rugani, R., Regolin, L., & Vallortigara, G. (2015) Numerical discrimination by frogs (Bombina orientalis). Anim Cogn 18:219–229.Google Scholar
Stein, B.E., & Meredith, M.A. (1993) The Merging of the Senses. MIT Press, Cambridge, MA.Google Scholar
Steriade, M., Jones, E.G., & McCormick, D.A. (1997) Thalamus. Vol. 1: Organization and Function. Elsevier, Amsterdam.Google Scholar
Steriade, M., & Paré, D. (2007) Gating in Cerebral Networks. Cambridge University Press, Cambridge, UK.Google Scholar
Striedter, G. (1991) Auditory, electrosensory, and mechanosensory lateral line pathways through the forebrain in channel catfishes. J Comp Neurol 312:311–331.Google Scholar
Striedter, G.F. (1999) Homology in the nervous system: of characters, embryology and levels of analysis. In: Bock, G.R., & Cardew, G. (Eds.), Homology (Novartis Foundation Symposium 222). John Wiley & Sons, Chichester, UK, pp. 158–172.Google Scholar
Striedter, G.F., & Northcutt, R.G. (2020) Brains through Time: A Natural History of Vertebrates. Oxford University Press, Oxford, UK.Google Scholar
Ströhmann, B., Schwarz, D.W.F., & Puil, E. (1994) Mode of firing and rectifying properties of nucleus ovoidalis neurons in the avian auditory thalamus. J Neurophysiol 71:1351–1360.Google Scholar
Suárez, J., Andreu, M.J., Heredia, R., Dávila, J.C., & Guirado, S. (2002) A putative striato-dorsal thalamic pathway in lizards. Brain Res Bull 57:533–535.Google Scholar
Suárez, J., Dávila, J.C., Real, M.Á., & Guirado, S. (2005) Distribution of GABA, calbindin and nitric oxide synthase in the developing chick entopallium. Brain Res Bull 66:441–444.Google Scholar
Suárez, J., Dávila, J.C., Real, M.Á., Guirado, S., & Medina, L. (2006) Calcium-binding proteins, neuronal nitric oxide synthase, and GABA help to distinguish different pallial areas in the developing and adult chicken. I. Hippocampal formation and hyperpallium. J Comp Neurol 497:751–771.Google Scholar
Sugahara, F., Murakami, Y., Adachi, N., & Kuratani, S. (2013) Evolution of the regionalization and patterning of the vertebrate telencephalon: what can we learn from cyclostomes? Curr Opin Genet Devel 23:475–483.Google Scholar
Sugahara, F., Murakami, Y., Pascual-Anaya, J., & Kuratani, S. (2017) Reconstructing the ancestral vertebrate brain. Develop Growth Differ 59:163–174.Google Scholar
Sugahara, F., Pascual-Anaya, J., Oisi, Y., Kuraku, S., Aota, S., Adachi, N., Takagi, W., Hirai, T., Sato, H., Murakami, Y., & Kuratani, S. (2016) Evidence from cyclostomes for complex regionalization of the ancestral vertebrate brain. Nature 531: 97–100.Google Scholar
Sur, M., & Rubenstein, J.L.R. (2005) Patterning and plasticity of the cerebral cortex. Sci 310:805–810.Google Scholar
Suryanarayana, S.M., Pérez-Fernández, J., Robertson, B., & Grillner, S. (2020) The evolutionary origin of visual and somatosensory representation in the vertebrate pallium. Nat Ecol Evol 4:639–651.Google Scholar
Suryanarayana, S.M., Robertson, B., Wallén, P., & Grillner, S. (2017) The lamprey pallium provides a blueprint of the mammalian layered cortex. Curr Biol 27:3264–3277.Google Scholar
Suzuki, I.K., & Hirata, T. (2012) Evolutionary conservation of neocortical neurogenetic program in the mammals and birds. Bioarchitec 2: 124–129.Google Scholar
Suzuki, I.K., & Hirata, T. (2013) Neocortical neurogenesis is not really “neo”: a new evolutionary model derived from a comparative study of chick pallial development. Dev Growth Differ 55:173–187.Google Scholar
Suzuki, I.K., Kawasaki, T., Gojobori, T., & Hirata, T. (2012) The temporal sequence of the mammalian neocortical neurogenic program drives mediolateral pattern in the chick pallium. Dev Cell 22:863–870.Google Scholar
Swanson, L.W., & Petrovich, G.D. (1998) What is the amygdala? Trends Neurosci 21:323–331.Google Scholar
Szele, F.G., Chin, H.K., Rowlson, M.A., & Cepko, C.L. (2002) Sox-9 and cDachsund-2 expression in the developing chick telencephalon. Mech Dev 112:179–182.Google Scholar
Tosa, Y., Hirao, A., Matsubara, I., Kawaguchi, M., Fukui, M., Kuratani, S., & Murakami, Y. (2015) Development of the thalamo-dorsal ventricular ridge tract in the Chinese soft-shelled turtle, Pelodiscus sinensis. Develop Growth Differ 57:40–57.Google Scholar
Tosches, M.A., Yamawaki, T.M., Naumann, R.K., Jacobi, A.A., Tushev, G., & Laurent, G. (2018) Evolution of pallium, hippocampus, and cortical cell types revealed by single-cell transcriptomes in reptiles. Sci 360:881–888.Google Scholar
Ulinski, P.S. (1983) Dorsal Ventricular Ridge: A Treatise on Forebrain Organization in Reptiles and Birds. John Wiley, New York.Google Scholar
van der Meij, J., Martinez-Gonzalez, D., Beckers, G.J.L., & Rattenborg, N.C. (2019) Intra-“cortical” activity during avian non-REM and REM sleep: variant and invariant traits between birds and mammals. Sleep J 42:1–13.Google Scholar
Veenman, C.L., Medina, L., & Reiner, A. (1997) Avian homologues of mammalian intralaminar, mediodorsal and midline thalamic nuclei: immunohistochemical and hodological evidence. Brain Behav Evol 49:78–98.Google Scholar
Vernier, P. (2017) The brains of teleost fishes. In: Kaas, J.H., & Striedter, G. (Eds.), Evolution of Nervous Systems. Vol. 1: The Evolution of the Nervous Systems in Nonmammalian Vertebrates, 2nd ed.Elsevier, Amsterdam, pp. 59–75.Google Scholar
Vila Pouca, C., Gervais, C., Reed, J., Michard, J., & Brown, C. (2019) Quantity discrimination in Port Jackson sharks incubated under elevated temperatures. Behav Ecol Sociobiol 73:93. doi:10.1007/s00265-019-2706-8.Google Scholar
von Bayern, A.M.P., Danel, S., Auersperg, A.M.I., Mioduszewska, B., & Kacelnik, A. (2018) Compound tool construction by New Caledonian crows. Sci Reports 8:15676. doi:10.1038/s41598-018-33458-z.Google Scholar
von Fersen, L., Wynne, C.D.L., & Delius, J.D. (1990) Deductive reasoning in pigeons. Naturwissench 77:548–549.Google Scholar
Wagner, G.P. (1999) A research programme for testing the biological homology concept. In Bock, G.R., & Cardew, G. (Eds.), Homology (Novartis Foundation Symposium 222). John Wiley & Sons, Chichester, pp. 125–140.Google Scholar
Wagner, G.P. (2014) Homology, Genes, and Evolutionary Innovation. Princeton University Press, Princeton, NJ.Google Scholar
Wagner, G.P., & Misof, B.Y. (1992) Evolutionary modification of regenerative capability in vertebrates: a comparative study on teleost pectoral fin regeneration. J Exp Zool 261:62–78.Google Scholar
Watanabe, M. (1987) Synaptic organization of the nucleus dorsolateralis anterior thalami in the Japanese quail (Coturnix coturnis japonica). Brain Res 401:92–112.Google Scholar
Watanabe, S., Sakamoto, J., & Wakita, M. (1995) Pigeons’ discrimination of paintings by Monet and Picasso. J Exp Anal Behav 63:165–174.Google Scholar
Westhoff, G., Roth, G., & Straka, H. (2004) Topographic representation of vestibular and somatosensory signals in the anuran thalamus. Neurosci 124:669–683.Google Scholar
Wild, J.M. (1987) The avian somatosensory system: connections of regions of body representation in the forebrain of the pigeon. Brain Res 412:205–223.Google Scholar
Wild, J.M. (1997) The avian somatosensory system: the pathway from wing to Wulst in a passerine (Chloris chloris). Brain Res 759:122–134.Google Scholar
Wild, J.M., Arends, J.J., & Zeigler, H.P. (1985) Telencephalic connections of the trigeminal system in the pigeon (Columba livia): a trigeminal sensorimotor circuit. J Comp Neurol 234:441–464.Google Scholar
Wild, J.M., Karten, H.J., & Frost, B.J. (1993) Connections of the auditory forebrain in the pigeon (Columba livia). J Comp Neurol 337:32–62.Google Scholar
Wild, J.M., & Williams, M.N. (2000) Rostral Wulst in passerine birds. I. Origin, course, and termination of an avian pyramidal tract. J Comp Neurol 416:429–450.Google Scholar
Wyzisk, K., & Neumeyer, C. (2007) Perception of illusory surfaces and contours in goldfish. Vis Neurosci 24:291–298.Google Scholar
Yamamoto, K., & Bloch, S. (2017) Overview of brain evolution: lobe-finned fish vs. ray-finned fish. In: Watanabe, S., Hofman, M.A., & Shimizu, T. (Eds.), Evolution of the Brain, Cognition, and Emotion in Vertebrates. Springer Japan KK, Tokyo, pp. 3–33.Google Scholar
Yamamoto, K., & Reiner, A. (2007) Is the avian dorsal ventricular ridge (DVR) homologous to the mammalian cerebral cortex or to the amygdala? Evaluating hypotheses by assessing homologous projection pathways to the telencephalon. In Watanabe, S., & Hofman, M.A. (Eds.), Integration of Comparative Neuroanatomy and Cognition. Keio University Press, Tokyo, pp. 75–96.Google Scholar
Zeier, H., & Karten, H.J. (1971) The archistriatum of the pigeon: organization of afferent and efferent connections. Brain Res 31:313–326.Google Scholar
Zhu, D., Lustig, K.H., Bifulco, K., & Keifer, J. (2005) Thalamocortical connections in the pond turtle Pseudemys scripta elegans. Brain Behav Evol 65:278–292.Google Scholar