Alejandro Otero’s research while affiliated with National Scientific and Technical Research Council and other places

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Publications (95)


Hindlimb biomechanics of Lagosuchus talampayensis (Archosauria, Dinosauriformes), with comments on skeletal morphology
  • Article

December 2024

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13 Reads

Journal of Anatomy

Alejandro Otero

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Peter J Bishop

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Lagosuchus talampayensis is a small‐bodied (~0.5 m long) Late Triassic dinosauriform archosaur from Argentina. Lagosuchus long has been a pivotal taxon for reconstructing the evolution of form and function on the dinosaur lineage. This importance is because it has a mix of ancestral archosaurian traits, such as a small pelvis with a mostly closed acetabulum lacking prominences that would restrict hip mobility much, with derived “dinosaurian” traits such as bipedalism, proximally shifted thigh muscle insertions, elongate hindlimbs, “advanced mesotarsal” ankle joints and digitigrade feet. Here, to quantify key functional traits related to the locomotor biomechanics of Lagosuchus , we build a three‐dimensional musculoskeletal model, focussing on morphofunctional analysis of the pelvic limb. We survey skeletal material that we have digitised, pointing out hitherto undescribed features and elements, many of which are from taxa other than Lagosuchus . Next, we select ideal elements amongst these to construct a composite model, and articulate adjacent body segments into joints, then estimate body shape including centre of mass, and add muscle paths to create a musculoskeletal model. Finally, we use two methods to quantify the hindlimb muscle parameters (“architecture”) in the model. We find that they produce similar estimates of force‐generating capacities, and compare these data to the few available data from other archosaurs in an evolutionary context, to reconstruct fundamental patterns of changes in muscle architecture and pelvic limb morphology. Our model forms a valuable basis for future quantitative analyses of locomotor function and its evolution in early archosaurs, and an example of how to navigate decision‐making for modelling problematic specimens.


They all floated in the cretaceous: new rebbachisaurid (Sauropoda, Diplodocoidea) with a highly pneumatized skeleton from the Upper Cretaceous (lower Cenomanian) of Patagonia, Argentina

August 2024

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90 Reads

Lucas N. Lerzo

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[...]

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Extant Phylogenetic Bracket (EPB) framework used in this work. Silhouettes of crocodilian and bird are from phylopic.org; silhouette of Skorpiovenator, credit to Joseph Shanks (https://www.deviantart.com/paleojoe).
Osteological correlates observed in the right ilium of Skorpiovenator (MMCh‐PV 48). (a) Detail of m. iliotibialis 1 and 2 (black arrows) and median swelling (white arrows) which marks the boundary between m. iliofemoralis externus and m. iliofibularis. (b) Anteroventral region of the ilium in lateroventral view showing the “preacetabular fossa” (white arrows) in which m. puboischiofemoralis internus 1 passed by. (c) Pubis in anterior view showing the scars (black arrows) for m. puboischiofemoralis externus 1. (d) Ischium in posterolateral view showing origin of m. flexor tibialis internus 3 and mm. aductores femores. (e) proximal ischium in lateral view. (f) Proximal pubis in lateral view, white arrows indicate striations for m. puboischiofemoralis internus 1. a, acetabulum; ADD 1, m. adductor femoris 1; ADD 2, m. adductor femoris 2; AMB, ambiens tubercle; fb, brevis fossa; fo, obturator foramen; FTI3, m. flexor tibialis internus 3; pab, preacetabular blade; PIFE 1, m. puboischiofemoralis externus 1; PIFI 1, m. puboischiofemoralis internus 1; pp, pubic peduncle; pu, pubis. Scale bars: 10 cm (ilium miniature), 5 cm (a–f), and 1 cm (close‐up in C).
Pelvic muscles inferred for Skorpiovenator bustingorryi (MMCh‐PV 48). (a) Pelvic girdle in lateral view; reconstructed ischium and pubis are shown in dotted lines. (b) Pelvic girdle and reconstructed pubis in anterior view. ADD 1, m. adductor femoris 1; ADD 2, m. adductor femoris 2; AMB, m. ambiens; CFB, m. caudofemoralis brevis; FTE, m. flexor tibialis externus; FTI3, m. flexor tibialis internus 3; IFE, m. iliofemoralis externus; ILFB, m. iliofibularis; IT 1–3, m. iliotibialis 1–3; ITC, m. iliotrochantericus caudalis; PIFE 1–3, m. puboischiofemoralis externus 1–3; PIFI 1–2, m. puboischiofemoralis internus 1–2.
Osteological correlates observed in the right femur of Skorpiovenator bustingorryi (MMCh‐PV 48). (a) Proximal femur in anterior view; white arrows indicate anterior intermuscular line. (b) Distal femur in anterior view; black arrow indicates distal extent of m. femorotibialis externus. (c) Proximal femur in posterior view; white arrows indicate rugosities for mm. puboischiofemorales insertion. (d) Detail of the distal femur in posterior view. (e) Posterolateral view of the femoral shaft showing the posterior intermuscular line. (f) Close‐up of the fourth trochanter in posteromedial view; white arrows show a faint intermuscular line over the fourth trochanter itself. 4t, fourth trochanter; ac, adductor crest; ail, anterior intermuscular line; cfl, m. caudofemoralis longus; fh, femoral head; FHL, m. flexor hallucis longus; GC, mm. gastrocnemii; gt, greater trochanter; FMTI, m. femorotibialis internus; ife, m. iliofemoralis externus; istr; m. ischiotrochantericus; itc, m. iliotrochantericus caudalis; lf4t, lateral fossa of fourth trochanter; mdc, mediodistal crest; pife 1–3, m. puboischiofemoralis externus 1–3; pifi 1–2, m. puboischiofemoralis internus 1–2; pil, posterior intermuscular line; pf, popliteal fossa; pr, promontory; tc, tibial condyle; ts, trochanteric shelf. Scale bars: 5 cm (a, b, e) and 2 cm (c, d, f).
Femoral muscle attachments inferred for Skorpiovenator bustingorryi (MMCh‐PV 48). (a) Posterior view. (b) Anterior view. (c) Posterolateral view. Muscle origins are marked in capital letters and red coloring; muscle insertions are marked in lowercase and blue coloring. add 1, m. adductor femoris 1; add 2, m. adductor femoris 2; cfb, m. caudofemoralis brevis; cfl, m. caudofemoralis longus; FDL, m. flexor digitorum longus; FHL, m. flexor hallucis longus; FMTE, m. femorotibialis externus; FMTI, m. femorotibialis internus; GL, m. gastrocnemius lateralis; ife, m. iliofemoralis externus; istr; m. ischiotrochantericus; itc, m. iliotrochantericus caudalis; pife 1–3, m. puboischiofemoralis externus 1–3; pifi 1–2, m. puboischiofemoralis internus. Scale bar equals 5 cm.

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Appendicular myology of Skorpiovenator bustingorryi: A first attempt to reconstruct pelvic and hindlimb musculature in an abelisaurid theropod
  • Article
  • Publisher preview available

July 2024

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595 Reads

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1 Citation

We present the pelvic and hindlimb musculature of the abelisaurid Skorpiovenator bustingorryi, constituting the most comprehensive muscle reconstruction to date in ceratosaur theropods. Using extant phylogenetic bracket method, we reconstructed 39 muscles that can commonly found in extant archosaurs. Through the identification of bone correlates, we recognized thigh and hindlimb muscles including knee extensors, m. iliofibularis, m. flexor tibialis externus, mm. caudofemorales, mm. puboischiofemorales, and crus muscles important in foot extension and flexion (e.g., m. tibialis anterior, mm. gastrocnemii). Also, autopodial intrinsic muscles were reconstructed whose function involve extension (m. extensor digiti 2–4), flexion (mm. flexor digitorum brevis superficialis), interdigital adduction (m. interosseus dorsalis) and abduction (m. interosseous plantaris, m. abductor 4). Abelisaurids like Skorpiovenator show a deep pre‐ and postacetabular blade of the ilia and enlarged cnemial crests, which would have helped increasing the moment arm of muscles related to hip flexion and hindlimb extension. Also, pedal muscles related to pronation were probably present but reduced (e.g., m. pronator profundus). Despite some gross differences in the autopodial morphology in extant outgroups (e.g., crocodilian metatarsus and avian tarsometatarsus), the present study allows us to hypothesize several pedal muscles in Skorpiovenator. These muscles would not be arranged in tendinous bundles as in Neornithes, but rather the condition would be similar to that of crocodilians with several layers formed by fleshy bellies on the plantar and dorsal aspects of the metatarsus. The musculature of Skorpiovenator is key for future studies concerning abelisaurid biomechanics, including the integration of functional morphology and ichnological data.

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Hindlimb and pelvic anatomy of Caiman yacare (Archosauria, Pseudosuchia): Myology and osteological correlates with emphasis on lower leg and autopodial musculature

December 2023

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107 Reads

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4 Citations

Journal of Anatomy

The anatomy of the archosaurian pelvis and hindlimb has adopted a diversity of successful configurations allowing a wide range of postures during the evolution of the group (e.g., erect, sprawling). For this reason, thorough studies of the structure and function of the pelvic and hindlimb musculature of crocodylians are required and provide the possibility to expand their implications for the evolution of archosaurian locomotion, as well as to identify potential new characters based on muscles and their bony correlates. In this study, we give a detailed description of the pelvic and hindlimb musculature of the South American alligator Caiman yacare , providing comprehensive novel information regarding lower limb and autopodial muscles. Particularly for the pedal muscles, we propose a new classification for the dorsal and ventral muscles of the autopodium based on the organisation of these muscles in successive layers. We have studied the myology in a global background in which we have compared the Caiman yacare musculature with other crocodylians. In this sense, differences in the arrangement of m. flexor tibialis internus 1, m. flexor tibialis externus , m. iliofibularis , mm. puboischiofemorales internii 1 and 2, between Ca . yacare and other crocodylians were found. We also discuss the muscle attachments that have different bony correlates among the crocodylian species and their morphological variation. Most of the correlates did not exhibit great variation among the species compared. The majority of the recognised correlates were identified in the pelvic girdle; additionally, some bony correlates associated with the pedal muscles are highlighted here for the first time. This research provides a wide framework for future studies on comparative anatomy and functional morphology, which could contribute to improving the character definition used in phylogenetic analyses and to understand the patterns of musculoskeletal hindlimb evolution.


The appendicular skeleton of Rinconsaurus caudamirus (Sauropoda: Titanosauria) from the Upper Cretaceous of Patagonia, Argentina

October 2022

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218 Reads

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11 Citations

Cretaceous Research

Rinconsaurus caudamirus, from the Bajo de la Carpa Formation (Santonian), Río Negro, Argentina, is represented by several axial and appendicular elements from, at least, four specimens. The axial skeleton of this taxon was described in detail in a recent contribution, pending a complete analysis and description of its appendicular skeleton. This contribution focuses on the description of the appendicular skeleton of Rinconsaurus and its phylogenetic relationships, considering the new information provided here. Rinconsaurus clearly differs from other titanosaurs for the presence of several autapomorphic characters and for a unique association of characters, some of which are also present in lognkosaurians, aeolosaurines and saltasaurines titanosaurs, and by having a scapula with a scapular blade angled 65° with respect to the coracoid articulation, similar to that of Bellusaurus, Dreadnoughtus and Muyelensaurus. Equations for estimating body mass in sauropods based on long bone circumference suggest a body mass of at least 3-5 tonnes for the largest individuals of Rinconsaurus, being lighter than saltasaurines, but heavier than aeolosaurines. Rinconsaurus was incorporated into an expanded version of a phylogenetic data matrix along with several ontemporary South American titanosaurs. The resulting data matrix comprises 102 taxa scored for 431 characters, and our phylogenetic analysis retrieves Rinconsaurus as a member of the clade Rinconsauria. For its part, the clade Rinconsauria, in which Aeolosaurini is nested, is recovered within a diverse Lognkosauria. When the resulting trees are time calibrated and taking into account the position of Ninjatitan within Rinconsauria, there results that the possible origin of the clades Lognkosauria and Rinconsauria (among other titanosaur clades) could have occurred towards the beginning of the Early Cretaceous.


Appendicular osteology of Skorpiovenator bustingorryi (Theropoda, Abelisauridae) with comments on phylogenetic features of abelisaurids

September 2022

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312 Reads

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11 Citations

Journal of Systematic Palaeontology

Skorpiovenator bustingorryi is a derived abelisaurid theropod represented by a fairly complete skeleton from the Late Cretaceous sedimentary beds of north-western Patagonia. Although some features were described in the original paper, mainly related to the skull, the appendicular anatomy remains undescribed. The aim of the present contribution is to provide a detailed description and analysis of the available appendicular bones, including comparisons with other ceratosaurian theropods close to Skorpiovenator. In this way, new autapomorphies emerged to further distinguish Skorpiovenator from its relatives. Furthermore, a comprehensive phylogenetic analysis was performed and several characteristics of the hind limb, in particular some of the autopodium, resulted in the identification of new apomorphic traits for Ceratosauria and Abelisauridae. These features might prove to be useful for future phylogenetic analyses and may help to resolve the still confusing and debated internal relationships of abelisaurid theropods.




Citations (44)


... Both Mm. caudofemorales are a level II inference by Witmer's (1995) systematization, being in positions topologically similar to other theropods (e.g. ceratosaurs- Cerroni et al. 2024, early tetanurans-Lacerda et al. 2024, and late-diverging coelurosaurs-Carrano and Hutchinson 2002. ...

Reference:

New theropod dinosaur remains from the Upper Cretaceous of the Kem Kem Group (Eastern Morocco) clarify spinosaurid morphology
Appendicular myology of Skorpiovenator bustingorryi: A first attempt to reconstruct pelvic and hindlimb musculature in an abelisaurid theropod

... Sterli and de la Fuente, 2013;Gasparini et al., 2015;Oriozabala et al., 2020); snakes (Albino, 2000;Gómez et al., 2019); plesiosaurs (e.g. O'Gorman et al., 2013aO'Gorman et al., , 2013bGasparini et al., 2015); ornithischian (Gasparini et al., 2015), sauropod (Gasparini et al., 2015;Pérez-Moreno et al., 2024) and theropod (Bonaparte, 1985;Lawver et al., 2011;Gasparini et al., 2015) dinosaurs; and mammals (e.g. Rougier et al., 2009Rougier et al., , 2021Harper et al., 2019). ...

A new titanosaur from the La Colonia Formation (Campanian-Maastrichtian), Chubut Province, Argentina
  • Citing Article
  • April 2024

... We obtained a total body mass of 24.56 kg for our model of Riojasuchus. This is very similar to an estimate of 28.33 kg (25.6% prediction error) from humeral and femoral minimal diaphyseal circumferences Note: Names [and acronyms] follow those used for Crocodylia (Hattori & Tsuihiji, 2021;Hutchinson, 2002;Pereyra et al., 2023;Romer, 1923a). Origins and insertions include levels of inference (Witmer, 1995) It is unclear where these differences arose from. ...

Hindlimb and pelvic anatomy of Caiman yacare (Archosauria, Pseudosuchia): Myology and osteological correlates with emphasis on lower leg and autopodial musculature
  • Citing Article
  • December 2023

Journal of Anatomy

... If the structure was absent, as in the case of the fore-and hindlimbs, the taxonomically closest material was used as a reference (e.g. Navarro et al. 2022, Pérez Moreno et al. 2023. ...

The appendicular skeleton of Rinconsaurus caudamirus (Sauropoda: Titanosauria) from the Upper Cretaceous of Patagonia, Argentina
  • Citing Article
  • October 2022

Cretaceous Research

... This character is found in derived abelisaurids such as the furileusaurian Brachyrostra Carnotaurus sastrei [48], Aucasaurus garridoi [34] and Koleken inakayali [3]. In the less derived Majungasaurus crenatissimus [42] and Skorpiovenator bustingorryi [49], the dorsal margin of the ilium is convex, while it is possibly undulated in Rahiolisaurus gujaratensis [50] and Ekrixinatosaurus novasi [51]. Interestingly, a straight dorsal margin is also present in Genusaurus sisteronis, from the Albian of France, a possible furileusaurian (see below and [34]). ...

Appendicular osteology of Skorpiovenator bustingorryi (Theropoda, Abelisauridae) with comments on phylogenetic features of abelisaurids
  • Citing Article
  • September 2022

Journal of Systematic Palaeontology

... Although the preservation of LAGs is affected by various factors (Chinsamy, 1993;Horner et al., 1999;Köhler et al., 2012), their annual cyclicity is generally accepted for both extant and extinct vertebrates (Cerda et al., 2022;Chinsamy et al., 2020;Chinsamy-Turan, 2005;Chinsamy & Warburton, 2021;Horner et al., 1999). ...

Palaeobiology of the early sauropodomorph Mussaurus patagonicus inferred from its long bone histology
  • Citing Article
  • July 2022

Palaeontology

... The terrestrial locomotor abilities of ornithosuchids have long been contentious. This controversy is important because they are an unusual clade of Triassic pseudosuchians that give insight into locomotor diversity in Archosauria, and thereby potentially also into longstanding broader controversies including the factors that may explain archosaurian survival versus extinction in the end-Triassic mass extinction (for a recent review, see Cuff et al., 2022). Ornithosuchids have been interpreted by different studies as bipedal (Walker, 1964), quadrupedal with bipedal faculties (Bonaparte, 1972) because of the disparity in length between their forelimbs and hindlimbs (especially their shorter manual vs. longer pedal digits); or perhaps quadrupedal Grinham et al., 2019;Kubo & Kubo, 2012;Sennikov, 2024). ...

Walking—and Running and Jumping—with Dinosaurs and Their Cousins, Viewed Through the Lens of Evolutionary Biomechanics

Integrative and Comparative Biology

... non-mammaliaform prozostrodonts Bonaparte & Migale, 2015;Gaetano et al., 2022;Hoffman et al., 2023;Kerber, Miron, et al., 2023;Kerber, Pretto, et al., 2023;Martinelli, Eltink, et al., 2017;Martinelli, Kammerer, et al., 2017;Stefanello et al., 2020). ...

A new cynodont from the Upper Triassic Los Colorados Formation (Argentina, South America) reveals a novel paleobiogeographic context for mammalian ancestors

... Bandeira et al. 2016, González-Riga et al. 2019. Although their remains are found on all continents, their greatest abundance in South America is remarkable (Carballido et al. 2022). Brazilian records of titanosaurs are concentrated mainly in Upper Cretaceous deposits of the Bauru Group (Kellner and Azevedo 1999, Santucci and Bertini 2006, Salgado and Carvalho 2008, Santucci and Arruda-Campos et al. 1997. ...

Titanosauria: A Critical Reappraisal of Its Systematics and the Relevance of the South American Record

... The fossil record of sauropodomorphs from the Caturrita Formation is particularly crucial because these forms represent the first step toward the acquisition of the typical "sauropodomorph body plan", characterized by reduced skulls, plant-eating teeth, elongated necks, and stout limbs (Leal et al., 2004;Müller et al., 2018;Otero & Peyre de Fabrègues, 2022). Whereas G. candelariensis and M. itaquii are known by a series of specimens, U. tolentinoi is poorly sampled. ...

Non-sauropodiform Plateosaurians: Milestones Through the “Prosauropod” Bauplan
  • Citing Chapter
  • April 2022