Demonstrates how embryogenesis arises from mechanical processes within living systems, highlighting implications for development and disease.
Biological development is traditionally interpreted through genetic and biochemical frameworks; however, living systems also operate as physical entities governed by mass distribution, thermal gradients, fluid dynamics, and mechanical constraints. This study advances an intrinsic gravito–thermo–biophysical framework, proposing that biological organization emerges from the integration of genetic regulation with universal physical principles. Within this context, embryogenesis is viewed as a gene-initiated but mechanically executed process, in which structural form arises through viscoelastic deformation of cellular assemblies exhibiting granular-like collective behaviour. Key morphogenetic stages—compaction, cavitation, gastrulation, and neurulation—are reinterpreted as threshold-driven reorganizations of mass involving stress redistribution, pressure gradients, fluid coupling, and energy dissipation. Development is further characterized by progressive mass accretion, thermogenesis, and structural differentiation. Germ layers are described as thermophysical domains that coordinate energy generation, transport, and regulation, while fluid systems—including amniotic fluid, circulation, and cerebrospinal fluid—provide buoyancy, convective transport, and pressure buffering, linking metabolic activity with structural organization. Stem cell behaviour is interpreted through microenvironmental anchorage and central constraint, where critical mass, density, and positional stability regulate potency and differentiation. Compositional evolution, including incorporation of elements such as iron and calcium, enhances thermal regulation and metabolic integration, while stress-field organization and fluid-mediated forces guide morphogenesis. This framework integrates biological, geophysical, and astrophysical perspectives, suggesting that living systems function as thermodynamically active, mechanically structured, and fluid-mediated assemblies. While not replacing molecular biology, it provides a complementary physical layer that offers new insights into development, thermoregulation, and disease, including cancer progression.
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Iresh Ranjan Bhattacharjee (2026) studied this question.
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