Whole body elongation drives coordinated vertebral shape evolution in Lake Malawi cichlid fishes

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This study investigates how vertebral morphology evolves in relation to whole-body elongation across the adaptive radiation of Lake Malawi cichlid fishes, focusing on evolutionary integration between precaudal and caudal vertebral domains and the contributions of vertebral count, centrum shape, and intervertebral spacing to body elongation. Using comparative evolutionary analyses, the authors find strong evolutionary integration between precaudal and caudal vertebral shape, with both domains changing along shared multivariate axes, while vertebral counts evolve independently, suggesting decoupling between “identity” (count) and shape. Whole-body elongation is associated with coordinated changes in vertebral and rib morphology, including larger centra, posterior displacement of neural and haemal spines, and increased rib curvature, whereas centrum elongation and intervertebral spacing do not further explain elongation beyond vertebral counts. This paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract

ABSTRACT Understanding how anatomical structures evolve requires disentangling the roles of integration and modularity in shaping morphological variation. The vertebral column, a serially repeated and regionally differentiated structure, provides a powerful system for investigating these processes. Here, we examine how vertebral morphology evolves in relation to whole-body elongation across the adaptive radiation of Lake Malawi cichlid fishes. We tested for evolutionary integration between the precaudal and caudal domains, as well as assessed the contributions of vertebral count, centrum shape, and intervertebral spacing on body elongation. We find strong evolutionary integration between the shapes of precaudal and caudal vertebrae, with both vertebral shapes varying along similar axes. Despite this, precaudal and caudal vertebral counts evolve independently, indicating a decoupling between the specification of identity and the development of their respective shapes. Whole-body elongation is significantly associated with coordinated changes in vertebral and rib morphology, including proportional increases in centrum size, posterior displacement of neural and haemal spines, and increased rib curvature. In contrast, centrum elongation and intervertebral spacing do not contribute to body elongation across the radiation. These results demonstrate that body elongation in cichlids necessitates integrated, multivariate changes in axial morphology. Our findings highlight the importance of morphological integration in facilitating coordinated evolutionary responses in anatomical systems.
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ABSTRACT Understanding how anatomical structures evolve requires disentangling the roles of integration and modularity in shaping morphological variation. The vertebral column, a serially repeated and regionally differentiated structure, provides a powerful system for investigating these processes. Here, we examine how vertebral morphology evolves in relation to whole-body elongation across the adaptive radiation of Lake Malawi cichlid fishes. We tested for evolutionary integration between the precaudal and caudal domains, as well as assessed the contributions of vertebral count, centrum shape, and intervertebral spacing on body elongation. We find strong evolutionary integration between precaudal and caudal vertebral shape, with both vertebral shapes varying along shared axes of multivariate shape change. Despite this, precaudal and caudal vertebral counts evolve independently, indicating a decoupling between the evolution of identity and morphology. Whole-body elongation is significantly associated with coordinated changes in vertebral and rib morphology, including proportional increases in centrum size, posterior displacement of neural and haemal spines, and increased rib curvature. In contrast, centrum elongation and intervertebral spacing do not independently explain body elongation beyond vertebral counts. These results demonstrate that body elongation in cichlids necessitates integrated, multivariate changes in axial morphology. Our findings highlight the importance of morphological integration in facilitating coordinated evolutionary responses in anatomical systems. Competing Interest Statement The authors have declared no competing interest.

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License: CC-BY-4.0