top of page

Evolutionary Constraints:

Why the Human Body Cannot Be Understood as an Ideal Design

Evolutionary constraints are the historical, structural, and developmental limits within which evolution shapes organisms. Rather than constructing perfect solutions from scratch, natural selection works with pre-existing materials, reorganizing existing forms and preserving many internal interdependencies among tissues, functions, and growth trajectories. From an osteopathic perspective, this means that the human body should not be viewed as an optimal machine that occasionally breaks down, but as a biological structure adapted within precise margins. Understanding evolutionary constraints thus helps explain why certain regions are efficient yet vulnerable, mobile yet unstable, resilient yet not infinitely modifiable. 

In evolutionary biology, the concept of constraint indicates that not all possible variations are actually available to selection. McKitrick describes phylogenetic constraint as the influence of evolutionary history on the directions change can take, while the most recent literature on the Extended Evolutionary Synthesis emphasizes the role of developmental constraints, modularity, and developmental bias in shaping biological forms. The central point is that adaptation does not eliminate history: it incorporates it. Every organism thus carries into the present both the selected solutions and the limitations arising from the way those solutions emerged. 

 

In the human body, bipedalism is one of the clearest examples. The transformation of the pelvis, lower limbs, and foot has made efficient and stable locomotion on two legs possible, but it has not created a system free of internal stresses. The literature on the human pelvis shows that upright posture and walking require a highly specialized skeletal and muscular configuration, in which form and function are closely interdependent. Even the medial arch of the foot, fundamental for bipedal locomotion, combines rigidity and mobility in a subtle way: it is precisely this functional sophistication that reveals how high-performing yet constrained the system is. 

For osteopathy, this has an important implication: the spine, pelvis, hip, knee, and foot cannot be interpreted as independent segments. They are parts of a chain derived from a shared evolutionary history and mutual constraints. When a region appears rigid or overloaded, the clinical question is not merely which tissue is suffering, but which functional architecture it is attempting to maintain. Evolutionary constraint does not equate to an anatomical limitation; rather, it indicates the realistic range within which the system can compensate. In this sense, thinking evolutionarily makes the very concept of structural normality more sober and precise. 

 

Bone tissue also clearly illustrates the issue of constraints. By analyzing human skeletal remains over the long term, Ruff has documented a decline in relative bone strength over the course of recent evolution, likely associated with changes in activity levels and mechanical demands. Ryan and Shaw have further shown that the slenderness of the modern Homo sapiens skeleton is largely the result of reduced loads during growth. This does not mean that bone is fragile “by mistake,” but that its plasticity operates within precise biological rules: it responds to load, but according to time windows, intensities, and limits that cannot be arbitrarily exceeded.

This point is crucial to avoid a common misunderstanding: evolutionary constraints do not negate plasticity, but rather define its scope. A human organism can change, learn, compensate, and reorganize itself; however, these processes occur within a framework defined by development, tissue integration, joint geometry, and phylogenetic history. The contemporary reinterpretation of Tinbergen’s four questions reminds us precisely that no biological phenomenon can be understood if current mechanisms, development, function, and evolutionary history are separated. In the osteopathic context, this framework invites us to interpret every bodily pattern not as a simple deviation from a standard, but as a possible outcome within a biologically constrained range. 

Essential Bibliography

  • McKitrick, M.C. (1993) ‘Phylogenetic constraint in evolutionary theory: Has it any explanatory power?’, Annual Review of Ecology and Systematics, 24, pp. 307–330.

  • Laland, K.N., Uller, T., Feldman, M.W., Sterelny, K., Müller, G.B., Moczek, A., Jablonka, E. and Odling-Smee, J. (2015) ‘The extended evolutionary synthesis: its structure, assumptions and predictions’, Proceedings of the Royal Society B: Biological Sciences, 282(1813), 20151019.

  • Lewis, C.L., Laudicina, N.M. and Khuu, A. (2017) ‘The human pelvis: variation in structure and function during gait’, The Anatomical Record, 300(4), pp. 633–642.

  • Arias-Martorell, J. (2018) ‘The morphology and evolutionary history of the glenohumeral joint’, Journal of Anatomy, 233(4), pp. 436–447.

  • Welte, L., Holowka, N.B., Kelly, L.A., Arndt, A. and Rainbow, M.J. (2023) ‘Mobility of the human foot’s medial arch helps enable upright bipedal locomotion’, Frontiers in Bioengineering and Biotechnology, 11, 1155439.

  • Ruff, C.B. (2005) ‘Mechanical determinants of bone form: insights from skeletal remains’, Journal of Musculoskeletal and Neuronal Interactions, 5(3), pp. 202–212.

  • Ryan, T.M. and Shaw, C.N. (2015) ‘Gracility of the modern Homo sapiens skeleton is the result of decreased biomechanical loading’, Proceedings of the National Academy of Sciences of the United States of America, 112(2), pp. 372–377.

  • Nesse, R.M. (2019) ‘Tinbergen’s four questions, organized: a response to Bateson and Laland’, Evolution, Medicine, and Public Health, 2019(1), p. 2.

bottom of page