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Andrew J. Irwin

Publications and source records attributed to Andrew J. Irwin.

5 recordsLinked to original sources

Costs and benefits of phytoplankton motility

The motility skills of phytoplankton have evolved and persisted over millions of years, primarily in response to factors such as nutrient and light availability, temperature and viscosity gradients, turbulence, and predation pressure. Phytoplankton motility is broadly categorized into swimming and buoyancy regulation. Despite studies in the literature exploring the motility costs and benefits of phytoplankton, there remains a gap in our integrative understanding of direct and indirect energy expenditures, starting from when an organism initiates movement due to any biophysical motive, to when the organism encounters intracellular and environmental challenges. Here we gather available pieces of this puzzle from literature in biology, physics, and oceanography to paint an overarching picture of our current knowledge. The characterization of sinking and rising behavior as passive motility has resulted in the concept of sinking and rising internal efficiency being overlooked. We define this efficiency based on any energy dissipation associated with processes of mass density adjustment, as exemplified in structures like vacuoles, gas vesicles, and frustules. We propose that sinking and rising are active motility processes involving non-visible mechanisms, as species demonstrate active and rapid strategies in response to turbulence, predation risk, and gradients of nutrients, light, temperature, and viscosity. In swimmers, internal and external motility efficiencies have been extensively explored in theoretical studies, yet they are largely neglected in energetic estimates within marine and freshwater sciences. Identifying the dissipative processes associated with swimming and buoyancy-regulating machinery offers deeper insight into motility costs relative to an organism's total metabolic rate.

physics.bio-ph

piCurve: an R package for modeling photosynthesis-irradiance curves

Photosynthesis-irradiance (PI) curves are foundational for quantifying primary production, parameterizing ecosystem and biogeochemical models, and interpreting physiological acclimation to light. Despite their broad use, researchers lack a unified, reproducible toolkit to fit, compare, and diagnose the many PI formulations that have accumulated over the last century. We introduce piCurve, an R package that standardizes the modeling of PI relationships, with a library of widely used light-limited, light-saturated, and photoinhibited formulations and a consistent statistical framework for estimation and comparison. With the total of 24 PI models, piCurve supports mean squared error (MSE) and maximum likelihood estimation (MLE), provides uncertainty quantification via information matrix (Hessian), and includes automated, data-informed initialization to improve convergence. Utilities classify PI data into light-limited, light-saturated, and photoinhibited regions, while plotting and 'tidy' helpers streamline workflow and reporting. Together, these features enable reproducible analyses and fair model comparisons, including for curves exhibiting a plateau followed by photoinhibition.

stat.AP

Parameterization of Photoinhibition For Phytoplankton

Mathematical models of photosynthesis-irradiance relationships in phytoplankton are used to compute integrated water-column photosynthetic rates and predict primary production. Models typically ignore an important phenomenon observed in most experiments: photosynthetic rate remains constant over a range of irradiances before declining due to photoinhibition. Here we develop an approach that captures both photoinhibition and this plateau. We test six new models of photoinhibition and ten more photoinhibition models from the literature against a database of 1808 photosynthesis-irradiance curves exhibiting photoinhibition. The best model improves adjusted R2 by 6-37% and reduces RMSE by 15-70% compared to existing models. In the best model, photoinhibition is phenomenologically described by multiplication by a saturating function of the reciprocal of irradiance, simplifies to the widely-used Jassby & Platt photosynthesis-irradiance curve in the absence of photoinhibition, and only requires one new parameter. This photoinhibition parameter identifies the onset of photoinhibition and is the rate of decrease in photosynthetic rate at that irradiance. Simulations show that while parameter values vary up to 40% across existing models, particularly with and without photoinhibition, our representation of photoinhibition does not affect the interpretation or numerical values of parameters compared to the corresponding model without photoinhibition.

q-bio.OT

Extending the Monod Model of Microbial Growth with Memory

Monod's model describes the growth of microorganisms using a hyperbolic function of extracellular resource concentration. Under fluctuating or limited resource concentrations this model performs poorly against experimental data, motivating the more complex Droop model with a time-varying internal storage pool. We extend the Monod model to incorporate memory of past conditions, adding a single parameter motivated by a fractional calculus analysis. We show how to interpret the memory element in a biological context and describe its connection to a resource storage pool. Under nitrogen starvation at non-equilibrium conditions, we validate the model with simulations and empirical data obtained from lab cultures of diatoms (T. pseudonana and T. weissflogii) and prasinophytes (Micromonas sp. and O. tauri), globally influential phytoplankton taxa. Using statistical analysis, we show that our Monod-memory model estimates the growth rate, cell density, and resource concentration as well as the Droop model while requiring one less state variable. Our simple model may improve descriptions of phytoplankton dynamics in complex earth system models at a lower computational cost than is presently achievable.

q-bio.PE

Memory and mutualism in species sustainability: a time-fractional Lotka-Volterra model with harvesting

We first present a predator-prey model for two species and then extend the model to three species where the two predator species engage in mutualistic predation. Constant effort harvesting and the impact of by-catch issue are also incorporated. Necessary sufficient conditions for the existence and stability of positive equilibrium points are examined. It is shown that harvesting is sustainable, and the memory concept of the fractional derivative damps out oscillations in the population numbers so that the system as a whole settles on an equilibrium quicker than it would with integer time derivatives. Finally, some possible physical explanations are given for the obtained results. It is shown that the stability requires the memory concept in the model.

math.DS