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      Broad similarities in shoulder muscle architecture and organization across two amniotes: implications for reconstructing non-mammalian synapsids

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          Abstract

          The evolution of upright limb posture in mammals may have enabled modifications of the forelimb for diverse locomotor ecologies. A rich fossil record of non-mammalian synapsids holds the key to unraveling the transition from “sprawling” to “erect” limb function in the precursors to mammals, but a detailed understanding of muscle functional anatomy is a necessary prerequisite to reconstructing postural evolution in fossils. Here we characterize the gross morphology and internal architecture of muscles crossing the shoulder joint in two morphologically-conservative extant amniotes that form a phylogenetic and morpho-functional bracket for non-mammalian synapsids: the Argentine black and white tegu Salvator merianae and the Virginia opossum Didelphis virginiana. By combining traditional physical dissection of cadavers with nondestructive three-dimensional digital dissection, we find striking similarities in muscle organization and architectural parameters. Despite the wide phylogenetic gap between our study species, distal muscle attachments are notably similar, while differences in proximal muscle attachments are driven by modifications to the skeletal anatomy of the pectoral girdle that are well-documented in transitional synapsid fossils. Further, correlates for force production, physiological cross-sectional area (PCSA), muscle gearing (pennation), and working range (fascicle length) are statistically indistinguishable for an unexpected number of muscles. Functional tradeoffs between force production and working range reveal muscle specializations that may facilitate increased girdle mobility, weight support, and active stabilization of the shoulder in the opossum—a possible signal of postural transformation. Together, these results create a foundation for reconstructing the musculoskeletal anatomy of the non-mammalian synapsid pectoral girdle with greater confidence, as we demonstrate by inferring shoulder muscle PCSAs in the fossil non-mammalian cynodont Massetognathus pascuali.

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          Functional and clinical significance of skeletal muscle architecture.

          Skeletal muscle architecture is the structural property of whole muscles that dominates their function. This review describes the basic architectural properties of human upper and lower extremity muscles. The designs of various muscle groups in humans and other species are analyzed from the point of view of optimizing function. Muscle fiber arrangement and motor unit arrangement is discussed in terms of the control of movement. Finally, the ability of muscles to change their architecture in response to immobilization, eccentric exercise, and surgical tendon transfer is reviewed. Future integrative physiological studies will provide insights into the mechanisms by which such adaptations occur. It is likely that muscle fibers transduce both stress and strain and respond by modifying sarcomere number in a way more suited to the new biomechanical environment. Copyright 2000 John Wiley & Sons, Inc.
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            Using false discovery rates for multiple comparisons in ecology and evolution

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              Variable gearing in pennate muscles.

              Muscle fiber architecture, i.e., the physical arrangement of fibers within a muscle, is an important determinant of a muscle's mechanical function. In pennate muscles, fibers are oriented at an angle to the muscle's line of action and rotate as they shorten, becoming more oblique such that the fraction of force directed along the muscle's line of action decreases throughout a contraction. Fiber rotation decreases a muscle's output force but increases output velocity by allowing the muscle to function at a higher gear ratio (muscle velocity/fiber velocity). The magnitude of fiber rotation, and therefore gear ratio, depends on how the muscle changes shape in the dimensions orthogonal to the muscle's line of action. Here, we show that gear ratio is not fixed for a given muscle but decreases significantly with the force of contraction (P < 0.0001). We find that dynamic muscle-shape changes promote fiber rotation at low forces and resist fiber rotation at high forces. As a result, gearing varies automatically with the load, to favor velocity output during low-load contractions and force output for contractions against high loads. Therefore, muscle-shape changes act as an automatic transmission system allowing a pennate muscle to shift from a high gear during rapid contractions to low gear during forceful contractions. These results suggest that variable gearing in pennate muscles provides a mechanism to modulate muscle performance during mechanically diverse functions.
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                Author and article information

                Contributors
                Journal
                PeerJ
                PeerJ
                PeerJ
                PeerJ
                PeerJ
                PeerJ Inc. (San Diego, USA )
                2167-8359
                18 February 2020
                2020
                : 8
                : e8556
                Affiliations
                [1 ]Museum of Comparative Zoology, Concord Field Station and Department of Organismic and Evolutionary Biology, Harvard University , Cambridge, MA, USA
                [2 ]Concord Field Station and Department of Organismic and Evolutionary Biology, Harvard University , Cambridge, MA, USA
                [3 ]Museum of Comparative Zoology and Department of Organismic and Evolutionary Biology, Harvard University , Cambridge, MA, USA
                Author information
                http://orcid.org/0000-0002-2451-4239
                Article
                8556
                10.7717/peerj.8556
                7034385
                32117627
                568b90b8-9d70-472a-ab5b-88d2b3152f3b
                © 2020 Fahn-Lai et al.

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited.

                History
                : 9 September 2019
                : 13 January 2020
                Funding
                Funded by: National Science Foundation
                Award ID: DEB-1754459
                Funded by: Department of Organismic and Evolutionary Biology at Harvard University
                Funded by: Robert A. Chapman Fellowship
                Funded by: Wetmore Colles fund
                This project was supported by National Science Foundation Grant No. DEB-1754459 (Stephanie E. Pierce), the Department of Organismic and Evolutionary Biology at Harvard University (Philip Fahn-Lai), and the Robert A. Chapman Fellowship (Philip Fahn-Lai). Publication costs were supported by the Wetmore Colles fund (Philip Fahn-Lai). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Paleontology
                Zoology
                Anatomy and Physiology

                shoulder,forelimb,mammals,non-mammalian synapsid,musculoskeletal function,posture,locomotion

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