Endocranial anatomy of the fossil furnariid <i>Pseudoseisura cursor</i> (Aves, Passeriformes): paleoecological perspectives and evolutionary implications
Centro de Investigaciones en Ciencias de la Tierra (CICTERRA), Facultad de Ciencias Exactas, Físicas y Naturales (FCEFyN), Universidad Nacional de Córdoba (UNC), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) - Ingenieur Ismael Bordabehere y Av. Haya de la Torre, Ciudad Universitaria, Córdoba, Argentina
Demmel Ferreira, María M. 2026. “Endocranial Anatomy of the Fossil Furnariid Pseudoseisura Cursor (Aves, Passeriformes): Paleoecological Perspectives and Evolutionary Implications”. El Hornero 41 (1). https://doi.org/10.56178/eh.v41i1.1530.
Furnariidae is a family endemic to the Neotropics and is one of the most diverse families of Passeriformes, and although it is one of the Neotropical families with the best fossil record, in Passeriformes in general the fossil record is scarce, which can make it difficult to interpret the evolution of the order in general. Pseudoseisura cursor, from the Ensenadan (Early–Middle Pleistocene) of Buenos Aires Province, Argentina, is considered the sister taxon of the extant species of the genus. This study describes the endocranial anatomy of this species and compares it with that of other extant Furnariidae to infer ecological aspects. A 3D model of the endocranium (i.e., a proxy for the brain) was created from micro-CT scans obtained from the holotype, which was described and measured (linear and surface-based measurements). Its body mass and endocranial volume were calculated, as well as its auditory capacities. Compared to the Brown Cacholote(Pseudoseisura lophotes), the endocranium of P. cursor shows general similarities but presents specific differences, such as greater dorsoventral development of the Wulsts and longer olfactory bulbs and flocculi, possibly related to its ancestral condition or functional adaptations. Although P. cursor had a greater body mass relative to the Brown Cacholote, its brain was proportionally smaller, with a volume of 9.73 times its body mass (23.59 times in the Brown Cacholote), which could be linked to the trend of body size reduction in extant species and the functional modularity of the brain. Additionally, P. cursor exhibited auditory capacities similar to those of Rufous Hornero (Furnarius rufus) and Narrow-billed Woodcreeper(Lepidocolaptes angustirostris), possibly due to a similar habitat.
Atoji Y, Sarkar S, Wild JM (2016) Proposed homology of the dorsomedial subdivision and V-shaped layer of the avian hippocampus to Ammon’s horn and dentate gyrus, respectively. Hippocampus 26(12):1608-1617. https://doi.org/10.1002/hipo.22660
Aylor D (1972) Sound transmission through vegetation in relation to leaf area density, leaf width and breadth of canopy. Journal of the Acoustical Society of America 51:411-414. https://doi.org/10.1121/1.1912852
Balanoff AM, Smaers JB, Turner AH (2016) Brain modularity across the theropod–bird transition: testing the influence of flight on neuroanatomical variation. Journal of Anatomy 229(2):204-214. https://doi.org/10.1111/joa.12403
Balanoff AM, Bever GS (2017) The Role of Endocasts in the Study of Brain Evolution. En: Kaas J (ed) Evolution of Nervous Systems 2ed vol. 1. Elsevier, Oxford, Pp. 223-241
Belton W (1984) Birds of Rio Grande do Sul, Brazil. Part 1: Rheidae through Furnariidae. Bulletin of the American Museum of Natural History 178:369-636
Boncoraglio G, Saino N (2007) Habitat structure and the evolution of bird song: a meta-analysis of the evidence for the acoustic adaptation hypothesis. Functional Ecology 21(1):134-142. https://doi.org/10.1111/j.1365-2435.2006.01207.x
Breazile JE, Kuenzel WJ (1993) Systema nervosum centrale. En: Baumel J, King A, Breazile J, Evans H, Berge J (eds) Nomina Anatomica Avium, 2ed (Pp. 493-554). Nuttall Ornithological Club.erebellum, 6:168-176
Brenowitz EA, Arnold AP (1986) Interspecific comparisons of the size of neural song control regions and song complexity in duetting birds: evolutionary implications. Journal of Neurosciences 6(10):2875-2879. https://doi.org/10.1523/JNEUROSCI.06-10-02875.1986
Chiappe LM, Navalón G, Martinelli AG, Carvalho IDS, Miloni Santucci R, Wu YH, Field DJ (2024) Cretaceous bird from Brazil informs the evolution of the avian skull and brain. Nature 635(8038):376-381. https://doi.org/10.1038/s41586-024-08114-4
Claramunt S, Rinderknecht A (2005) A new fossil furnariid from the Pleistocene of Uruguay, with remarks on nasal type, cranial kinetics, and relationships of the extinct genus Pseudoseisuropsis. The Condor: Ornithological Applications 107(1):114-127. https://doi.org/10.1093/condor/107.1.114
Demmel Ferreira MM, Degrange FJ, Tirao GA (2024) Brain surface morphology and ecological and macroevolutionary inferences of avian New World suboscines (Aves, Passeriformes, Tyrannides). Journal of Comparative Neurology 532(4):e25617. doi: 10.1002/cne.25617
Early CM, Iwaniuk AN, Ridgely RC, Witmer LM (2020) Endocast structures are reliable proxies for the sizes of corresponding regions of the brain in extant birds. Journal of Anatomy 237(6):1162-1176. https://doi.org/10.1111/joa.13285
Field DJ, Lynner C, Brown C, Darroch SA (2013) Skeletal correlates for body mass estimation in modern and fossil flying birds. PLOS One 8(11):e82000. https://doi.org/10.1371/journal.pone.0082000
Fjeldså J, Irestedt M, Ericson PGP (2005) Molecular data reveal some major adaptational shifts in the early evolution of the most diverse avian family, the Furnariidae. Journal of Ornithology 146:1-13. https://doi.org/10.1007/s10336-004-0054-5
Hall ZJ, Street SE, Healy SD (2013) The evolution of cerebellum structure correlates with nest complexity. Biology Letters 9(6): 20130687. https://doi.org/10.1098/rsbl.2013.0687
Hansen P (1979) Vocal learning: its role in adapting sound structures to long-distance propagation and a hypothesis on its evolution. Animal Behaviour 27:1270-1271. https://doi.org/10.1016/0003-3472(79)90073-3
Harris CM (1966) Absorption of sound in air versus humidity and temperature. Journal of the Acoustical Society of America 40:148-159. https://doi.org/10.1121/1.1910031
Healy SD, Rowe C (2007) A critique of comparative studies of brain size. Proceedings of the Royal Society B: Biological Sciences 274(1609):453-464. https://doi.org/10.1098/rspb.2006.3748
Hofer H (1952) Der Gestaltwandel des Schädels der Säugetiere und Vögel. mit besonderer Berücksichtigung der Knickungstypen und der Schädelbasis. Verhandlungen der Anatomischen Gesellschaft 99:102-126
Irestedt M, Fjeldså J, Ericson PGP (2006) Evolution of the ovenbird-woodcreeper assemblage (Aves: Furnariidae)—Major shifts in nest architecture and adaptive radiation. Journal of Avian Biology 37:260-272. https://doi.org/10.1111/j.2006.0908-8857.03612.x
Iwaniuk AN, Wylie DR (2006) The evolution of stereopsis and the Wulst in caprimulgiform birds: a comparative analysis. Journal of Comparative Physiology A 192:313-1326. https://doi.org/10.1007/s00359-006-0161-2
Iwaniuk AN, Dean KM, Nelson JE (2004) A mosaic pattern characterizes the evolution of the avian brain. Proceedings: Biological Sciences 271(suppl_4):S148-S151. https://doi.org/10.1098/rsbl.2003.0127
Iwaniuk AN, Dean KM, Nelson JE (2005) Interspecific allometry of the brain and brain regions in parrots (Psittaciformes): comparisons with other birds and primates. Brain Behavior and Evolution 65: 40-59. https://doi.org/10.1159/000081110
Juárez R (2021) Scimitar-billed Woodcreeper (Drymornis bridgesii), version 2.0. En: Billerman SM (ed) Birds of the World. Cornell Lab of Ornithology, Ithaca, NY, EUA. https://doi.org/10.2173/bow.scbwoo4.02
Kratter AW, Sillett TS, Chesser RT, O’Neill JP, Parker III TA, Castillo A (1993) Avifauna of a Chaco locality in Bolivia. Wilson Bulletin 105:114-141. [URL: https://www.jstor.org/stable/4163253]
Ksepka DT., Balanoff AM, Smith NA, …, Zanno LE, Jarvis ED, Smaers JB (2020) Tempo and pattern of avian brain size evolution. Current Biology 30(11):2026-2036. https://doi.org/10.1016/j.cub.2020.03.060
Kurochkin EN, Dyke GJ, Saveliev SV, Pervushov EM, Popov EV (2007) A fossil brain from the Cretaceous of European Russia and avian sensory evolution. Biology Letters 3(3):309-313. https://doi.org/10.1098/rsbl.2006.0617
Lopes LE, Fernandes AM, Marini MA (2003) Consumption of vegetable matter by Furnarioidea. Ararajuba 11:235-239
Marantz CA, Aleixo A, Bevier LR, Patten MA (2020) Narrow-billed Woodcreeper (Lepidocolaptes angustirostris), version 1.0. En: del Hoyo J, Elliott A, Sargatal J, Christie DA, de Juana E (eds) Birds of the World. Cornell Lab of Ornithology, Ithaca, NY, EUA. https://doi.org/10.2173/bow.nabwoo1.01
Michelsen A, Larsen ON (1983) Strategies for acoustic communication in complex environments. En: Huber F, Markl H (eds) Neuroethology and Behavioral Physiology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-69271-0_23
Noriega JI (1998) Aspectos paleozoogeográficos del registro de los Passeriformes (Aves) del Plioceno y Pleistoceno en la provincia de Buenos Aires. V Jornadas Geológicas y Geofísicas Bonaerenses 1:65-71
Ohlson J, Fjeldså J, Ericson PGP (2008) Tyrant flycatchers coming out in the open: Phylogeny and ecological radiation of Tyrannidae (Aves, Passeriformes). Zoologica Scripta 37:315-335. https://doi.org/j.1463-6409.2008.00325.x
Remsen Jr JV (2020) Buff-browed Foliage-gleaner (Syndactyla rufosuperciliata), version 1.0. En: del Hoyo J, Elliott A, Sargatal J, Christie DA, de Juana A (eds) Birds of the World. Cornell Lab of Ornithology, Ithaca, NY, EUA. https://doi.org/10.2173/bow.bbfgle1.01
Remsen Jr JV (2024) Brown Cacholote (Pseudoseisura lophotes), version 1.1. En: del Hoyo J, Elliott A, Sargatal J, Christie DA, de Juana A, Smith MG (eds) Birds of the World. Cornell Lab of Ornithology, Ithaca, NY, EUA. https://doi.org/10.2173/bow.brncac1.01.1
Remsen, Jr., J. V. & A. Bonan (2020). Rufous Hornero (Furnarius rufus), version 1.0. En: del Hoyo J, Elliott A, Sargatal J, Christie DA, de Juana A (eds) Birds of the World. Cornell Lab of Ornithology, Ithaca, NY, EUA. https://doi.org/10.2173/bow.rufhor2.01
Ridgely RS, Tudor G (1994) The birds of South America. Volume II. The suboscine passerines. University of Texas Press, Austin, Texas, EUA
Smaers JB, Vanier DR (2019) Brain size expansion in primates and humans is explained by a selective modular expansion of the cortico-cerebellar system. Cortex 118:292-305. https://doi.org/10.1016/j.cortex.2019.04.023
Stacho M, Herold C, Rook N, Wagner H, Axer M, Amunts K, Güntürkün O (2020) A cortex-like canonical circuit in the avian forebrain. Science 369(6511):eabc5534. https://doi.org/10.1126/science.abc5534
Stefanini I, Gómez RO, Tambussi CP (2016) Taxonomic reassessment of the Pleistocene Furnariidae (Passeriformes) Pseudoseisuropsis nehuen from the South American Pampas, a new species of the genus and phylogenetic relationships. Journal of Vertebrate Paleontology 36:e1100630. https://doi.org/10.1080/02724634.2016.1100630
Stingelin W (1957) Vergleichendmorphologische Untersuchungen am Vorderhirn der Vögel auf cytologischer undcytoarchitektonischer Grundlage. Basel, Verlag Helbing & Lichtenhahn. Lübeck, Alemania
Tambussi CP (2011) Paleoenvironmental and faunal inferences based upon the avian fossil record of Patagonia and Pampa: what works and what does not. Biological Journal of the Linnean Society 103:458-474. https://doi.org/10.1111/j.1095-8312.2011.01658.x
Tambussi CP, Degrange FJ, Ksepka DT (2015) Endocranial anatomy of Antarctic Eocene stem penguins: implications for sensory system evolution in Sphenisciformes (Aves). Journal of Vertebrate Paleontology 35:e981635. https://doi.org/10.1080/02724634.2015.981635
Tonni EP (1977) Un furnárido (Aves, Passeriformes) del Pleistoceno medio de la Provincia de Buenos Aires. Publicaciones del Museo Municipal de Ciencias Naturales de Mar del Plata Lorenzo Scaglia 2(6):141-147
Tonni EP, Noriega JI (2001) Una especie extinta de Pseudoseisura Reichenbach 1853 (Passeriformes: Furnariidae) del Pleistoceno de la Argentina: comentarios filogenéticos. Ornitología Neotropical 12(1):29-44. [URL: https://digitalcommons.usf.edu/ornitologia_neotropical/vol12/iss1/4]
Walsh SA, Barrett PM, Milner AC, Manley G, Witmer LM (2009) Inner ear anatomy is a proxy for deducing auditory capability and behaviour in reptiles and birds. Proceedings of the Royal Society B: Biological Sciences 276(1660):1355-1360. https://doi.org/10.1098/rspb.2008.1390
Walsh SA, Iwaniuk AN, Knoll MA, Bourdon E, Barrett PM, Milner AC, Nudds RL, Abel RL, Sterpaio PD (2013) Avian cerebellar floccular fossa size is not a proxy for flying ability in birds. PLoS One 8(6):e67176. https://doi.org/10.1371/journal.pone.0067176
Winkler DW, Billerman SM, Lovette IJ (2020) Ovenbirds and woodcreepers. En: Billermarn SM, Keeney BK, Rodewald PG, Schulenberg TS (eds) Birds of the World. Cornell Lab of Ornithology, Ithaca, NY, EUA. https://doi.org/10.2173/bow.furnar2.01
Witmer LW, Ridgely RC (2008) The paranasal air sinuses of predatory and armored dinosaurs (Archosauria: Theropoda and Ankylosauria) and their contribution to cephalic structure. The Anatomical Record 291:1362-1388. https://doi.org/10.1002/ar.20794
Witmer LM, Ridgely RC, Dufeau DL, Semones MC (2008) Using CT to peer into the past: 3D visualization of the brain and ear regions of birds, crocodiles, and nonavian dinosaurs. En: Endo H, Frey R (eds) Anatomical Imaging. Springer, Tokyo. https://doi.org/10.1007/978-4-431-76933-0_6
Wylie DR, Gutiérrez-Ibáñez C, Iwaniuk A (2015) Integrating brain, behavior, and phylogeny to understand the evolution of sensory systems in birds. Frontiers in Neuroscience 9:281. https://doi.org/10.3389/fnins.2015.00281