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Brain evolution by brain pathway duplication
Open accessAbstract
Understanding the mechanisms of evolution of brain pathways for complex behaviours is still in its infancy. Making further advances requires a deeper understanding of brain homologies, novelties and analogies. It also requires an understanding of how adaptive genetic modifications lead to restructuring of the brain. Recent advances in genomic and molecular biology techniques applied to brain research have provided exciting insights into how complex behaviours are shaped by selection of novel brain pathways and functions of the nervous system. Here, we review and further develop some insights to a new hypothesis on one mechanism that may contribute to nervous system evolution, in particular by brain pathway duplication. Like gene duplication, we propose that whole brain pathways can duplicate and the duplicated pathway diverge to take on new functions. We suggest that one mechanism of brain pathway duplication could be through gene duplication, although other mechanisms are possible. We focus on brain pathways for vocal learning and spoken language in song-learning birds and humans as example systems. This view presents a new framework for future research in our understanding of brain evolution and novel behavioural traits.
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“Second, analyses of brain gene expression profiles strongly suggest that songbirds and parrots independently evolved vocal learning pathways by duplication of preexisting, surrounding motor circuits (57, 58).”
From Birds have primate-like numbers of neurons in the forebrain (2016) · cites this paper as [58]
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Cites
Ohno, S. (1970) · doi:10.1007/978-3-642-86659-3 · Cited by 7,833 · cited 4×
“Other hypotheses posit that existing genes are modified, including changes in coding sequence, cis-regulatory motifs [16,17] or new alternative mRNA splice variants [18–21], a process known as subfunctionalization [12–14].”
BackgroundInfluentialFodor, J. A. (1983) · doi:10.7551/mitpress/4737.001.0001 · Cited by 7,734
Pinker, S. (1994) · doi:10.5860/choice.31-6014 · Cited by 5,271
The faculty of language: what is it, who has it, and how did it evolve?
Hauser, M. D., Chomsky, N., & Fitch, W. T. (2002) · Science · doi:10.1126/science.298.5598.1569 · Cited by 5,189
Evolution by gene duplication: An update
Zhang, J. (2003) · Trends in Ecology & Evolution · doi:10.1016/s0169-5347(03)00033-8 · Cited by 2,201 · cited 1×
“One of the duplicated genes may then acquire a mutation in coding or regulatory sequences, which enables it to acquire a new function that then undergoes selection, a process known as neofunctionalization [12–15].”
BackgroundWhole-genome analyses resolve early branches in the tree of life of modern birds
Jarvis, E. D., Mirarab, S., Aberer, A. J., Li, B., Houde, P., Li, C., Ho, S. Y. W., Faircloth, B. C., Nabholz, B., Howard, J. T., et al. (2014) · Science · doi:10.1126/science.1253451 · Cited by 1,901 · cited 3×
“With the recent availability of genomes across the avian [93,177,178] and eventually primate [179,180] family trees, it becomes possible to discover candidate genes.”
BackgroundSelf-citationDescending Pathways in Motor Control
Lemon, R. N. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.060407.125547 · Cited by 1,599 · cited 1×
“Based on these and other findings, it is generally proposed that the direct CM system of M1 is a recently evolved brain structure that conferred evolutionarily novel functions in the motor system in primates, including independent voluntary control of finger movements, which are more advanced in primates compared with…”
ResultThe Language Instinct: How the Mind Creates Language
Macneal, E. (1995) · ETC: A Review of General Semantics · doi:10.66774/etc_5201_105 · Cited by 1,525
Sex Chromosomes and Sex-Linked Genes
Ohno, S. (1967) · Monographs on endocrinology · doi:10.1007/978-3-642-88178-7 · Cited by 1,497 · cited 3×
“Other hypotheses posit that existing genes are modified, including changes in coding sequence, cis-regulatory motifs [16,17] or new alternative mRNA splice variants [18–21], a process known as subfunctionalization [12–14].”
BackgroundThe evolution of gene duplications: classifying and distinguishing between models
Innan, H., & Kondrashov, F. A. (2010) · Nature Reviews Genetics · doi:10.1038/nrg2689 · Cited by 1,338 · cited 1×
“Gene duplications have been found to influence the development and function of many organs and tissues, including brains, eyes and wings [11,139–147].”
Background
Flagged first, then by citations
10 of the 189 references couldn’t be matched to a known paper.
Research works printed but not linked: 11
- Merker B, 2012, Music, language, and human evolution
- Kaas JH, 1989, The evolution of complex sensory systems in mammals, J. Exp. Biol., 146, 165, 10.1242/jeb.146.1.165 · DOI
- 10.1037/e412952005-009 · DOI
- von Economo C, 1929, The cytoarchitectonics of the human cortex
- Kaas JH, 1982, Contributions to Sensory Physiology
- Finlay BL, 2005, Attention and performance XXI ‘process of change in brain and cognitive development’, 131
- Fitch WT, 2013, Language, music, and the brain, 499, 10.7551/mitpress/9548.003.0028 · DOI
- Nettl B, 2000, The origins of music, 463
- Friel JP, 1999, Evolution of complexity in motor patterns and jaw musculature of tetraodontiform fishes, J. Exp. Biol., 202, 867, 10.1242/jeb.202.7.867 · DOI
- Lauder GV, 1993, The skull, 113
- 10.1078/0944-2006-00022 · DOI
Cited by
Sorted by citations
Birds have primate-like numbers of neurons in the forebrain
Olkowicz, S., Kocourek, M., Lučan, R. K., Porteš, M., Fitch, W. T., Herculano-Houzel, S., & Němec, P. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1517131113 · Cited by 564
“Second, analyses of brain gene expression profiles strongly suggest that songbirds and parrots independently evolved vocal learning pathways by duplication of preexisting, surrounding motor circuits (57, 58).”
BackgroundArchitectures of neuronal circuits
Luo, L. (2021) · Science · doi:10.1126/science.abg7285 · Cited by 390
Vocal learning as a preadaptation for the evolution of human beat perception and synchronization
Patel, A. D. (2021) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2020.0326 · Cited by 115
Evolution of vocal learning and spoken language
Jarvis, E. D. (2019) · Science · doi:10.1126/science.aax0287 · Cited by 329
Self-citationKorlach, J., Gedman, G. L., Kingan, S. B., Chin, C.-S., Howard, J. T., Audet, J., Cantin, L. J., & Jarvis, E. D. (2017) · GigaScience · doi:10.1093/gigascience/gix085 · Cited by 244
Self-citationCerebellar nuclei evolved by repeatedly duplicating a conserved cell-type set
Kebschull, J. M., Richman, E. B., Ringach, N., Friedmann, D., Albarran, E., Kolluru, S. S., Jones, R. C., Allen, W. E., Wang, Y., Cho, S. W., et al. (2020) · Science · doi:10.1126/science.abd5059 · Cited by 262
The origins of the vocal brain in humans
Belyk, M., & Brown, S. (2017) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2017.03.014 · Cited by 144
“Chakraborty & Jarvis (2015) further observed that parrots, which are the most accomplished avian vocal learners, possess nested “shell” and “core” vocal systems.”
The functions of vocal learning in parrots
Bradbury, J. W., & Balsby, T. J. S. (2016) · Behavioral Ecology and Sociobiology · doi:10.1007/s00265-016-2068-4 · Cited by 122
“It thus may not take many generations of captive breeding before a parrot such as the budgerigar no longer acts, vocalizes, or develops in the ways that it did in nature.”
BackgroundInfluentialVertebrate brains and evolutionary connectomics: on the origins of the mammalian ‘neocortex’
Karten, H. J. (2015) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2015.0060 · Cited by 125
Tempo and Pattern of Avian Brain Size Evolution
Ksepka, D. T., Balanoff, A. M., Smith, N., Bever, G. S., Bhullar, B.-A. S., Bourdon, E., Braun, E. L., Burleigh, J. G., Clarke, J. A., Colbert, M. W., et al. (2020) · Current Biology · doi:10.1016/j.cub.2020.03.060 · Cited by 149
Self-citationEvolution of central neural circuits: state of the art and perspectives
Roberts, R. J. V., Pop, S., & Prieto-Godino, L. L. (2022) · Nature reviews. Neuroscience · doi:10.1038/s41583-022-00644-y · Cited by 109
Mapping Human Laryngeal Motor Cortex during Vocalization
Eichert, N., Papp, D., Mars, R. B., & Watkins, K. E. (2020) · Cerebral Cortex · doi:10.1093/cercor/bhaa182 · Cited by 89
“Additional support for a duplication theory also comes from genetic profiling analyses comparing gene expressions in song-learning birds and humans (Pfenning et al. 2014; Chakraborty and Jarvis 2015).”
BackgroundDevelopmental and genetic mechanisms of neural circuit evolution
Tosches, M. A. (2017) · Developmental Biology · doi:10.1016/j.ydbio.2017.06.016 · Cited by 95
Brain evolution in social insects: advocating for the comparative approach
Godfrey, R. K., & Gronenberg, W. (2019) · Journal of Comparative Physiology A · doi:10.1007/s00359-019-01315-7 · Cited by 90
Phylogenetic origins of biological cognition: convergent patterns in the early evolution of learning
van Duijn, M. (2017) · Interface Focus · doi:10.1098/rsfs.2016.0158 · Cited by 60
Social calls provide novel insights into the evolution of vocal learning
Sewall, K. B., Young, A. M., & Wright, T. F. (2016) · Animal Behaviour · doi:10.1016/j.anbehav.2016.07.031 · Cited by 60
“First, the specialized neural mechanisms that underpin vocal learning (Bolhuis et al., 2010; Chakraborty et al., 2015; Feenders et al., 2008; Jarvis, 2004) may be difficult to evolve (Chakraborty & Jarvis, 2015; Isler & Schaik, 2006; Mink et al., 1981).”
BackgroundMaking Feeding Decisions in the Drosophila Nervous System
Miroschnikow, A., Schlegel, P., & Pankratz, M. J. (2020) · Current Biology · doi:10.1016/j.cub.2020.06.036 · Cited by 76
The Molecular Basis of Human Brain Evolution
Enard, W. (2016) · Current Biology · doi:10.1016/j.cub.2016.09.030 · Cited by 55
von Eugen, K., Tabrik, S., Güntürkün, O., & Ströckens, F. (2020) · The Journal of Comparative Neurology · doi:10.1002/cne.24878 · Cited by 66
“Moreover, Psittacines and Passeriformes are both vocal learners, and thus their cerebral bauplan includes unique vocal and auditory nuclei, which are not present in nonvocal learners (Chakraborty & Jarvis, 2015; Reiner, Perkel, Mello, & Jarvis, 2004).”
BackgroundThe hippocampus of birds in a view of evolutionary connectomics
Herold, C., Schlömer, P., Mafoppa-Fomat, I., Mehlhorn, J., Amunts, K., & Axer, M. (2018) · Cortex · doi:10.1016/j.cortex.2018.09.025 · Cited by 58
Epigenetic code and insect behavioural plasticity
Maleszka, R. (2016) · Current Opinion in Insect Science · doi:10.1016/j.cois.2016.03.003 · Cited by 68
Fruitless mutant male mosquitoes gain attraction to human odor
Basrur, N. S., Obaldia, M. E. D., Morita, T., Herre, M., von Heynitz, R. K., Tsitohay, Y. N., & Vosshall, L. B. (2020) · eLife · doi:10.7554/elife.63982 · Cited by 53
A sensorimotor control framework for understanding emotional communication and regulation
Williams, J. H. G., Huggins, C. F., Zupan, B., Willis, M. L., Rheenen, T. E. V., Sato, W., Palermo, R., Ortner, C. N. M., Krippl, M., Kret, M. E., et al. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.02.014 · Cited by 60
Apes, feathered apes, and pigeons: differences and similarities
Güntürkün, O., Ströckens, F., Scarf, D., & Colombo, M. (2017) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2017.03.003 · Cited by 55
Roux, J., Liu, J., & Robinson‐Rechavi, M. (2017) · Molecular Biology and Evolution · doi:10.1093/molbev/msx199 · Cited by 59
“The expanded toolkit of nervous genes likely provided opportunities for regulatory network rewiring and new functions to evolve (Chakraborty and Jarvis 2015; Evlampiev and Isambert 2007; Oakley and Rivera 2008).”
BackgroundConnectivity and the search for specializations in the language-capable brain
Mars, R. B., Eichert, N., Jbabdi, S., Verhagen, L., & Rushworth, M. F. S. (2018) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2017.11.001 · Cited by 41
“It has been proposed that analogous modifications have occurred in the human lineage [39].”
Couto, A., Young, F. J., Atzeni, D., Marty, S., Melo-Flórez, L., Hebberecht, L., Monllor, M., Neal, C. R., Cicconardi, F., McMillan, W. O., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-39618-8 · Cited by 43
“Under this model, increased behavioural precision, or diversi fi cation, can occur through replication of established cell types and circuits within generally conserved networks 4,5 .”
Birdsong Learning and Culture: Analogies with Human Spoken Language
Bruno, J. H., Jarvis, E., Liberman, M., & Tchernichovski, O. (2021) · Annual Review of Linguistics · doi:10.1146/annurev-linguistics-090420-121034 · Cited by 43
“Consistent with these observations, a strong case has been made that vocal learning brain pathways evolved out of motor-learning pathways that control complex, learned nonvocal behaviors (Feenders et al. 2008, Tokarev et al. 2011, Chakraborty & Jarvis 2015, Jarvis 2019).”
BackgroundSelf-citationVocal learning: Beyond the continuum
Martins, P. T., & Boeckx, C. A. (2020) · PLoS Biology · doi:10.1371/journal.pbio.3000672 · Cited by 51
“Indeed, Chakraborty and Jarvis [54] acknowledge it might not be straightforward to reconcile the core/shell system with the VLC. Finally, in the VLC, humans alone are considered high-end vocal learners, whereas parrots are classified at a level just below, referred to as complex vocal learners.”
BackgroundInfluentialAudet, J., Couture, M., & Jarvis, E. D. (2023) · Science · doi:10.1126/science.adh3428 · Cited by 49
Self-citationVahaba, D. M., & Remage‐Healey, L. (2018) · Hormones and Behavior · doi:10.1016/j.yhbeh.2018.03.007 · Cited by 37
“songbirds and humans share the rare and remarkable suite of traits for learned vocalizations (Chakraborty and Jarvis, 2015; Prather et al., 2017), understanding the role of neuroestrogens in communication learning and processing may lead to important translational dis-”
Cahill, J. A., Armstrong, J. C., Deran, A., Khoury, C. J., Paten, B., Haussler, D. H., & Jarvis, E. D. (2021) · Genome Research · doi:10.1101/gr.275989.121 · Cited by 43
“…expansion of forebrain size and increased pallium (i.e., cortical) neuron density in song-birds ’ and parrots ’ brains (Olkowicz et al. 2016), which in turn may have accommodated their extra vocal learning brain pathway (Feenders et al. 2008; Chakraborty and Jarvis 2015; Chakraborty et al. 2015).”
Self-citationThe Brains of Reptiles and Birds
Güntürkün, O., Stacho, M., & Ströckens, F. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-804042-3.00007-5 · Cited by 32
Ballarin, C., Povinelli, M., Granato, A., Panin, M., Corain, L., Peruffo, A., & Cozzi, B. (2016) · PLoS ONE · doi:10.1371/journal.pone.0154580 · Cited by 33
“However, the evolution of brain pathways that promote complex behavioral traits remains enigmatic [43].”
BackgroundA modular circuit coordinates the diversification of courtship strategies
Coleman, R. T., Morantte, I., Koreman, G. T., Cheng, M. L., Ding, Y., & Ruta, V. (2024) · Nature · doi:10.1038/s41586-024-08028-1 · Cited by 32
“Similar mechanisms have been proposed to underlie the elaboration of cerebellar nuclei 59 and the evolution of pallial–striatal circuits 58 in vertebrates.”
Distributed physiology and the molecular basis of social life in eusocial insects
Friedman, D., Johnson, B. R., & Linksvayer, T. A. (2020) · Hormones and Behavior · doi:10.1016/j.yhbeh.2020.104757 · Cited by 35
“In mammals, it has been proposed that brain pathways can arise via duplication and subspecialization, and thus elaborate over evolutionary time analogously to gene duplication (Chakraborty and Jarvis, 2015).”
BackgroundAvian brains: Insights from development, behaviors and evolution
Nomura, T., & Izawa, E. (2017) · Development Growth & Differentiation · doi:10.1111/dgd.12362 · Cited by 34
“4, blue lines), respectively, which is called ‘song system’ (Konishi 1985; Brainard & Doupe 2000; Matsunaga & Okanoya 2009; Mooney 2009; Chakraborty & Jarvis 2015).”
BackgroundColony expansions underlie the evolution of army ant mass raiding
Chandra, V., Gal, A., & Kronauer, D. J. C. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2026534118 · Cited by 28
“Vocal learning circuits in birds are thought to have evolved via the duplication and modification of ancestral motor circuits (29).”
BackgroundSpontaneity and diversity of movement to music are not uniquely human.
Keehn, R. J. J., Iversen, J., Schulz, I., & Patel, A. D. (2019) · Current Biology · doi:10.1016/j.cub.2019.05.035 · Cited by 30
Syllable as a Synchronization Mechanism That Makes Human Speech Possible
Xu, Y. (2024) · Brain Sciences · doi:10.3390/brainsci15010033 · Cited by 23
Evolution of vocal patterns: tuning hindbrain circuits during species divergence
Barkan, C. L., Zornik, E., & Kelley, D. (2017) · Journal of Experimental Biology · doi:10.1242/jeb.146845 · Cited by 26
Whole-body connectome of a segmented annelid larva
Verasztó, C., Jasek, S., Gühmann, M., Bezares-Calderón, L. A., Williams, E. A., Shahidi, R., & Jékely, G. (2025) · eLife · doi:10.1101/2024.03.17.585258 · Cited by 21
“Duplication and divergence of circuits was also proposed as a possible mechanism for the evolution of brain pathways for vocal learning in song-learning birds, spoken language in humans ( Chakraborty and Jarvis, 2015 ) and other circuits ( Roberts et al., 2022 ).”
Kuwabara, T., Kohno, H., Hatakeyama, M., & Kubo, T. (2023) · Science Advances · doi:10.1126/sciadv.add4201 · Cited by 28
Araya‐Salas, M., Smith‐Vidaurre, G., Mennill, D. J., González‐Gómez, P. L., Cahill, J. A., & Wright, T. F. (2019) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2019.0666 · Cited by 27
Nonlinear growth: an origin of hub organization in complex networks
Bauer, R., & Kaiser, M. (2017) · Royal Society Open Science · doi:10.1098/rsos.160691 · Cited by 22
A non-canonical retina-ipRGCs-SCN-PVT visual pathway for mediating contagious itch behavior
Gao, F., Ma, J., Yu, Y., Gao, X.-F., Bai, Y., Sun, Y., Liu, J., Liu, X., Barry, D. M., Wilhelm, S. J., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111444 · Cited by 25
“Genetic duplication and adoption from the pre-existing spinal GRPR neural circuits could be possible mechanisms by which neural circuits of contagious itch arose during evolution (Chakraborty and Jarvis, 2015).”
Plattner, H., & Verkhratsky, A. (2018) · Cell Calcium · doi:10.1016/j.ceca.2018.04.001 · Cited by 30
Beat-based dancing to music has evolutionary foundations in advanced vocal learning
Patel, A. D. (2024) · BMC Neuroscience · doi:10.1186/s12868-024-00843-6 · Cited by 18
“2 Schematic of core and shell systems for vocal learning in a parrot brain [83].”
BackgroundInfluentialGraïc, J.-M., Peruffo, A., Ballarin, C., & Cozzi, B. (2017) · The Anatomical Record · doi:10.1002/ar.23593 · Cited by 18
A dual larynx motor networks hypothesis
Belyk, M., Eichert, N., & McGettigan, C. (2021) · Philosophical Transactions of the Royal Society B · doi:10.1098/rstb.2020.0392 · Cited by 17
“Chakraborty & Jarvis (2015) proposed that such a phenotype could arise by mutations that cause the entire network to duplicate as an ensemble, in line with a previous proposal that the avian song system itself may have evolved as a specialization from a pre-existing limb and body motor network…”
BackgroundMoving beyond domain-specific versus domain-general options in cognitive neuroscience.
Asano, R., Boeckx, C., & Fujita, K. (2021) · Cortex; a journal devoted to the study of the nervous system and behavior · doi:10.31234/osf.io/euxy9 · Cited by 17
Vocal Imitation in Sensorimotor Learning Models: A Comparative Review
Pagliarini, S., Leblois, A., & Hinaut, X. (2020) · IEEE Transactions on Cognitive and Developmental Systems · doi:10.1109/tcds.2020.3041179 · Cited by 20
“…by the laryngeal motor cortex (LMC), connect directly to vocal motor neurons (plain red arrows, lower panel) providing the motor output (controlling the larynx in humans or syrinx in birds) [14], [15]. is also called vocal production pathway, since it involves direct projections to motor neurons.”
BackgroundInfluentialCoupled Genomic Evolutionary Histories as Signatures of Organismal Innovations in Cephalopods
Ritschard, E. A., Whitelaw, B. L., Albertin, C. B., Cooke, I., Strugnell, J. M., & Simakov, O. (2019) · BioEssays · doi:10.1002/bies.201900073 · Cited by 32
Brain Size Associated with Foot Preferences in Australian Parrots
Kaplan, G., & Rogers, L. (2021) · Symmetry · doi:10.3390/sym13050867 · Cited by 16
“Even more puzzling, from a functional point of view, is, as Chakraborty and colleagues [38,39] discovered, that parrots have a core and shell song systems, i.”
BackgroundDuplications and domain-generality.
Endress, A. D. (2019) · Psychological Bulletin · doi:10.1037/bul0000213 · Cited by 15
Inhibitory and modulatory inputs to the vocal central pattern generator of a teleost fish
Rosner, E., Rohmann, K. N., Bass, A., & Chagnaud, B. (2018) · The Journal of comparative neurology · doi:10.1002/cne.24411 · Cited by 16
“The neuronal circuitry that generates these signals includes forebrain and midbrain regions and a single or multiple hindbrain vocal central pattern generators (CPGs, e.g., Bass, 2014; Chakraborty & Jarvis, 2015).”
BackgroundKorlach, J., Gedman, G. L., Kingan, S., Chin, C., Howard, J., Cantin, L. J., & Jarvis, E. (2017) · bioRxiv · doi:10.1101/103911 · Cited by 16
Self-citationEvolution of neural circuitry and cognition
Farnworth, M. S., & Montgomery, S. H. (2024) · Biology Letters · doi:10.1098/rsbl.2023.0576 · Cited by 19
“For example, circuits involved in avian song production [57,58] and electroreception in mormyrid fishes [17] likely involved circuit replication, while a specific conserved circuit motif is duplicated during cerebellar expansion in vertebrates [59].”
BackgroundZhao, Z.-L., Teoh, H. K., Carpenter, J., Nemon, F., Kardon, B., Cohen, I., & Goldberg, J. H. (2023) · bioRxiv · doi:10.1101/2023.05.04.539392 · Cited by 14
“At the neural level, though the songbird and parrot song systems are both nucleated and contain distinct anterior and posterior pathways, there are also important differences in the detailed connectivity likely related to the distinct effects of AFP inactivations 18–27 .”
BackgroundIs the Capacity for Vocal Learning in Vertebrates Rooted in Fish Schooling Behavior?
Larsson, M. L., & Abbott, B. W. (2018) · Evolutionary Biology · doi:10.1007/s11692-018-9457-8 · Cited by 17
“One possibility, is that the specialized neural mechanisms that underpin vocal learning (Bolhuis and Wynne 2009; Chakraborty and Jarvis 2015; Jarvis 2004) may simple be difficult to evolve on a structural or technical level (Chakraborty and Jarvis 2015; Isler and van Schaik 2006; Mink et al. 1981).”
BackgroundChakraborty, M., Chen, L., Fridel, E. E., Klein, M. E., Senft, R. A., Sarkar, A., & Jarvis, E. D. (2017) · Scientific Reports · doi:10.1038/s41598-017-00519-8 · Cited by 19
Self-citationMedina, C. A., Vargas, E., Munger, S. J., & Miller, J. E. (2022) · PLoS ONE · doi:10.1371/journal.pone.0265604 · Cited by 15
Wright, T. F., & Derryberry, E. (2021) · Neuroscience and Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.02.022 · Cited by 13
SRGAP2 and the gradual evolution of the modern human language faculty
Martins, P. T., Marí, M., & Boeckx, C. (2017) · bioRxiv · doi:10.1101/143248 · Cited by 13
Parallel executive pallio‐motor loops in the pigeon brain
Steinemer, A., Simon, A., Güntürkün, O., & Rook, N. (2024) · The Journal of comparative neurology · doi:10.1002/cne.25611 · Cited by 12
“In a revised scenario, HVC neurons might have evolved from ancestral motor circuits through duplication (Chakraborty & Jarvis, 2015) or the strengthening of these pathways (Petkov & Jarvis, 2012) that later specialized for vocal con-trol (Feenders et al., 2008).”
BackgroundNeural correlates of cognitively controlled vocalizations in a corvid songbird
Brecht, K. F., Westendorff, S., & Nieder, A. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112113 · Cited by 14
Schuppe, E. R., Cantin, L. J., Chakraborty, M., Biegler, M. T., Jarvis, E. R., Chen, C.-C., Hara, E., Bertelsen, M., Witt, C. C., Jarvis, E., et al. (2022) · PLoS Biology · doi:10.1371/journal.pbio.3001751 · Cited by 12
“For these reasons, it is proposed that vocal learning pathways might have arisen by the duplication of brain pathways from surrounding motor learning circuits, which subsequently become specialized for sets of genes involved in neural connectivity, physiology, and plasticity [2,4,7].”
BackgroundSelf-citationA conjecture about the neural basis of recursion in light of descent with modification
Boeckx, C. A. (2016) · Journal of Neurolinguistics · doi:10.1016/j.jneuroling.2016.08.003 · Cited by 7
What we talk about when we talk about biolinguistics
Martins, P. T., & Boeckx, C. (2016) · Linguistics Vanguard · doi:10.1515/lingvan-2016-0007 · Cited by 11
The Organization of Neocortex in Early Mammals
Kaas, J. H. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-804042-3.00032-4 · Cited by 12
Kaplan, G. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105621 · Cited by 15
“And why do parrots have an additional shell song control system, i.e. have brain structures meant for song even more complex than in songbirds (Chakraborty and Jarvis, 2015)?”
BackgroundA modular circuit architecture coordinates the diversification of courtship strategies in DrosophilaPreprint
Coleman, R. T., Morantte, I., Koreman, G. T., Cheng, M. L., Ding, Y., & Ruta, V. (2023) · bioRxiv · doi:10.1101/2023.09.16.558080 · Cited by 10
“striatal circuits of songbirds mediating vocal learning have been proposed to evolve via the duplication and diversification of ancestral motor learning circuits (83, 84).”
Introduction to ‘Origin and evolution of the nervous system’
Strausfeld, N. J., & Hirth, F. (2015) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2015.0033 · Cited by 15
Audition and Hemispheric Specialization in Songbirds and New Evidence from Australian Magpies
Kaplan, G. (2017) · Symmetry · doi:10.3390/sym9070099 · Cited by 9
Bridging the fields of cognition and birdsong with corvids
Liao, D. A., Moll, F. W., & Nieder, A. (2025) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2024.102965 · Cited by 8
Optimality Pressures toward Lateralization of Complex Brain Functions
Seoane, L. F. (2023) · Physical Review X · doi:10.1103/physrevx.13.031028 · Cited by 5
Vocal babbling in a wild parrot shows life history and endocrine affinities with human infants
Eggleston, R., Viloria, N., Delgado, S., Mata, A., Guerrero, H. Y., Kline, R. J., Beissinger, S., & Berg, K. S. (2022) · Proceedings of the Royal Society B · doi:10.1098/rspb.2022.0592 · Cited by 8
Cockatiels sing human music in synchrony with a playback of the melody
Seki, Y. (2021) · PLoS ONE · doi:10.1371/journal.pone.0256613 · Cited by 8
Modularity is the Bedrock of Natural and Artificial IntelligencePreprint
Salatiello, A. (2026) · arXiv (Cornell University) · doi:10.48550/arxiv.2602.18960 · Cited by 2
“This approach has already led to consolidated theories about the evolution of selected brain modules (Feenders et al., 2008; Chakraborty & Jarvis, 2015; Kebschull et al., 2020) and to increasingly detailed descriptions of the evolutionary origin of the existing modular organization (Cisek, 2019;…”
Vocal repertoire expansion in singing mice by co-opting a conserved midbrain circuit node
Zheng, X. M., Harpole, C. E., Davis, M. B., & Bandyopadhyay, A. (2025) · Current Biology · doi:10.1016/j.cub.2025.10.036 · Cited by 9
Unsolved morphogenesis problems and the hidden order
Melkikh, A. V. (2024) · Biosystems · doi:10.1016/j.biosystems.2024.105218 · Cited by 7
Chronic recording of cortical activity underlying vocalization in awake minipigs
Palma, M., Khoshnevis, M., Lion, M., Zenga, C., Kefs, S., Fallegger, F., Schiavone, G., Flandin, I. G., Lacour, S. P., & Yvert, B. (2021) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2021.109427 · Cited by 14
Alcamí, P., Totagera, S., Sohnius‐Wilhelmi, N., Leitner, S., Grothe, B., Frankl‐Vilches, C., & Gahr, M. L. (2021) · Biology · doi:10.3390/biology10111099 · Cited by 6
Fate of Duplicated Neural Structures
Seoane, L. F. (2020) · Entropy · doi:10.3390/e22090928 · Cited by 7
Selective expansion of motor cortical projections in the evolution of vocal noveltyPreprint
Isko, E. C., Harpole, C. E., Zheng, X. M., Zhan, H., Davis, M. B., Zador, A. M., & Banerjee, A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.13.612752 · Cited by 4
“Beyond such changes in brain architecture, other influential models predict that modified long-range connectivity among existing brain regions can lead to functional di-vergences [9, 24–26].”
BackgroundOrganizational Conservation and Flexibility in the Evolution of Birdsong and Avian Motor Control
Colquitt, B. M. (2022) · Brain Behavior and Evolution · doi:10.1159/000525019 · Cited by 8
“…output nucleus, sits at the medial end of AId and has similar gene expression and connectivity as its neighbor, suggesting that RA is a specialized motor control region derived from ancestral motor circuitry [Feenders et al., 2008; Chakraborty and Jarvis, 2015; Jarvis, 2019; Nevue et al., 2020].”
BackgroundThe role of sex chromosomes and sex hormones in vocal learning systems.
Choe, H., & Jarvis, E. (2021) · Hormones and Behavior · doi:10.1016/j.yhbeh.2021.104978 · Cited by 6
Self-citationCognitive instincts versus cognitive gadgets: A fallacy
Roige, A., & Carruthers, P. (2019) · Mind & Language · doi:10.1111/mila.12251 · Cited by 6
“For notice that copying-and-repurposing is quite common in biological evolution (Barrett, 2012; Chakraborty & Jarvis, 2015; Kaas, 1989; Marcus, 2004).”
BackgroundGenome-resolved biogeography of Phaeocystales, cosmopolitan bloom-forming algae
Füssy, Z., Lampe, R. H., Arrigo, K. R., Barry, K., Brisbin, M. M., Brussaard, C. P. D., Decelle, J., de Vargas, C., DiTullio, G. R., Elbourne, L. D. H., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-63565-1 · Cited by 10
Hickok, G. S. (2024) · BMC Neuroscience · doi:10.1186/s12868-024-00868-x · Cited by 4
“…don’t exhibit BPS, is that parrots and humans have a more complex vocal learning system, and (ii) that this complexity is related to the added ability of parrots and humans to control supra-syringeal/laryngeal vocal organs, which seems to involve a dual neural control system in both species [2, 3].”
BackgroundExploring Anatomical Links Between the Crow's Nidopallium Caudolaterale and Its Song System
Moll, F. W., Kersten, Y., Erdle, S., & Nieder, A. (2024) · bioRxiv · doi:10.1002/cne.70028 · Cited by 5
“…anatomical position and connectivity, several related hypotheses on the evolutionary origin of the song system have suggested that HVC might be a specialized part of NCL that could have diverged from NCL via pathway duplication (Farries 2001; Feenders et al. 2008; Chakraborty and Jarvis 2015).”
The Molecular Basis of Differentiation Wave Activity in Embryogenesis
Alicea, B., Bastani, S., Gordon, N. K., Crawford-Young, S. J., & Gordon, R. (2024) · bioRxiv · doi:10.1101/2024.06.04.597397 · Cited by 5
Vocal Learning and Songbirds: An Evolutionary Tale of Singing
Erickson, H. M. (2022) · Journal of Singing · doi:10.53830/xhji5745 · Cited by 5
Position-independent emergence of neocortical neuron molecular identity, connectivity and function
Roig‐Puiggros, S., Guyoton, M., Suchkov, D., Fortoul, A., Matteucci, G., Fièvre, S., Panzeri, A., Molochidis, N., Barcellini, F., Maino, E., et al. (2025) · Nature Neuroscience · doi:10.1038/s41593-025-02142-7 · Cited by 6
“Structure duplication followed by divergence is a driving force in brain evolution 29,30 and is thought to have underlaid the emergence of basal ganglia and cerebellar circuits 31,32 , bird and human vocal pathways 30,33 and higher-order cortical areas from primary sensory and motor ones 34–36 .”
FinchGPT: a Transformer based language model for birdsong analysis
Kobayashi, K., Matsuzaki, K., Taniguchi, M., Sakaguchi, K., Inui, K., & Abe, K. (2025) · arXiv.org · doi:10.48550/arxiv.2502.00344 · Cited by 4
“It have been suggested that the brain nuclei of songbirds have analogous regions in human brain with respect to their role in vocal control (Fig 4A) [36,37].”
The emergence of enhanced intelligence in a brain-inspired cognitive architecture
Schneider, H. (2024) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2024.1367712 · Cited by 10
“Genetic and developmental mechanisms have been put forward for the duplication of mammalian brain circuits and their divergence to new functions (e.g., Rakic, 2009; Chakraborty and Jarvis, 2015).”
BackgroundInfluentialThe emergence of compositionality in a brain-inspired cognitive architecture
Schneider, H. (2024) · Cognitive Systems Research · doi:10.1016/j.cogsys.2024.101215 · Cited by 7
Specific expansion of motor cortical projections in a singing mouse
Isko, E. C., Harpole, C. E., Zheng, X. M., Zhan, H., Davis, M. B., Zador, A. M., & Banerjee, A. (2026) · Nature · doi:10.1038/s41586-026-10458-y · Cited by 9
“Such expansion of specific neuronal projections have been proposed to expand behavioural repertoire, such as increased dexterity 23,48 and courtship songs 4 .”
InfluentialRunnqvist, E., & Kell, C. A. (2025) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2025.101573 · Cited by 2
Evolution of Telencephalon Anterior–Posterior Patterning through Core Endogenous Network Bifurcation
Sun, C., Yao, M., Xiong, R., Su, Y., Zhu, B., Chen, Y.-C., & Ao, P. (2024) · Entropy · doi:10.3390/e26080631 · Cited by 3
Metadata
- Authors
- Chakraborty, M., & Jarvis, E. D.
- Affiliations
- Howard Hughes Medical Institute (US)
- Corresponding author
- Chakraborty, Mukta
- Jarvis, Erich D.
- ORCID
- Jarvis, Erich D.
- Venue
- Philosophical Transactions of the Royal Society B: Biological Sciences
- Publisher
- The Royal Society
- Published
- 2015-12-19
- Volume
- 370
- Issue
- 1684
- Pages
- 20150056
- ISSN
- 0962-8436 (ISSN-L)
- 1471-2970
- PMC
- PMC4650129
- OpenAlex
- W2193504960
- Cited by
- 150
- References
- 189
- Citations by year
- 2026: 9 · 2025: 15 · 2024: 24 · 2023: 9 · 2022: 9 · 2021: 20 · 2020: 16 · 2019: 8 · 2018: 7 · 2017: 17 · 2016: 13 · 2015: 2
- FWCI
- 2.63
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Philosophical Transactions of the Royal Society B Biological Sciences (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DukeSpace (Duke University) (submittedVersion, cc-by-nc-nd)
- Funders
- Howard Hughes Medical Institute
- Topics
- Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Animal Vocal Communication and Behavior
- Social Sciences › Cultural Studies › Language and cultural evolution
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Keywords
- brain evolution, gene duplication, vocal learning, song learning, spoken language, complex behavior, nervous system evolution
- MeSH terms
- Animals, Birds, Brain, Biological Evolution, Humans, Neural Pathways, Vocalization, Animal
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