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Anderson M. Rodriguez

Publications and source records attributed to Anderson M. Rodriguez.

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An Entropy-initiated Coupled-Trait ODE Framework for Modeling Longitudinal Cohort Dynamics

This work introduces a minimal, information-theoretic dynamical framework for modeling longitudinal cohort data using an entropy-initiated system of coupled-trait ordinary differential equations (ECTO). For each survey wave, item-level Likert responses are compressed into a normalized Shannon entropy index that summarizes cross-sectional dispersion; this index is used to initialize the low-dimensional state variables of the autonomous ODE system. ECTO then tracks the interactions among a primary trait-like state, a secondary coupled state, and a latent environmental-stress component through phenomenological terms representing generic self-limitation, trade-offs, and feedback. Using data from the Swedish Adoption/Twin Study on Aging (SATSA), the framework reproduces broad cohort-level trajectories and is evaluated with leave-one-wave-out forecasting and comparisons against simple statistical baselines. A second longitudinal dataset of U.S. dental student data provides an external validation test, demonstrating that low-dimensional dynamics initialized from entropy measures can generalize across cohorts with different measurement instruments, demographic compositions, and timescales. Across both datasets, ECTO achieves stable out-of-sample performance, indicating that major cohort-level trends can be captured without assuming complex latent-variable models or time-varying causal inputs. Entropy here functions as a compact summary of population heterogeneity rather than a dynamical driver, and the coupled ODEs supply an interpretable alternative to high-dimensional or black box machine-learning approaches. This framework establishes a concise, transparent method for linking information-theoretic preprocessing with cohort-level dynamical modeling and provides a foundation for future multivariate or multi-cohort extensions.

q-bio.QM

Curvature-Induced Saturation in Catalytic Reaction Networks: A Differential Geometrical Framework for Modeling Chemical Complexity

The evolution of chemical reaction networks is often analyzed through kinetic models and energy landscapes, but these approaches fail to capture the deeper structural constraints governing complexity growth. In chemical reaction networks, emergent constraints dictate the organization of reaction pathways, limiting combinatorial expansion and determining stability conditions. This paper introduces a novel approach to modeling chemical reaction networks by incorporating differential geometry into the classical framework of reaction kinetics. By utilizing the Riemannian metric, Christoffel symbols, and a system-specific entropy-like term, we provide a new method for understanding the evolution of complex reaction systems. The approach captures the interdependence between species, the curvature of the reaction network's configuration space, and the tendency of the system to evolve toward more probable states. The interaction topology constrains the accessible reaction trajectories and the introduced differential geometrical approach allows analysis of curvature constraints which help us to understand pathway saturation and transition dynamics. Rather than treating reaction space as an unconstrained combinatorial landscape, we frame it as a structured manifold with higher order curvature describing a geodesic for system evolution under intrinsic constraints. This geometrical perspective offers a unique insight into pathway saturation, self-interruption, and emergent behavior in reaction networks, and provides a scalable framework for modeling large biochemical or catalytic systems.

q-bio.MN