Abstract
Seasonal transitions in biological systems are commonly described as linear metabolic responses to environmental cues such as temperature and resource availability. However, such approaches struggle to account for cross-species synchrony, abrupt phenological shifts, and the widespread breakdown of seasonal timing under contemporary ecological disruption.
Here, we propose a conceptual framework—Seasonal Phase Compression–Jump (SPCJ) dynamics—that reconceptualizes winter not as metabolic dormancy but as a structured compression phase in which organisms accumulate latent internal potential. This compression state is characterized by coordinated physiological reorganizations, including shifts in gas composition, pH gradients, microbial–mitochondrial energy partitioning, and modulation of neural conductivity.
Within this framework, spring emergence arises as a nonlinear transition triggered when accumulated latent phase potential exceeds a critical threshold, resulting in rapid activation, growth, and synchronization. This mechanism provides a unifying interpretation of hibernation, delayed implantation, overwintering strategies, and seasonal desynchronization across diverse taxa.
The SPCJ framework integrates concepts from nonlinear dynamics into seasonal biology and offers a generalized theoretical basis for biological timing. By formalizing seasonal transitions as phase-driven processes rather than gradual metabolic recovery, this work establishes a foundation for future empirical investigation and computational modeling of biological seasonality.
This framework is intended as a conceptual and hypothesis-generating model rather than a direct empirical claim.

This work is licensed under a Creative Commons Attribution 4.0 International License.
Copyright (c) 2026 Doha Lee (Author)
