Past Mathematical Biology and Ecology Seminar

Consumer-resource interactions are central to ecology, as all organisms rely on consuming resources to survive. Functional responses describe how a consumer's feeding rate changes with resource availability, influenced by processes like searching for, capturing, and handling resources. To study functional responses, experiments typically measure the amount of food consumed—often in discrete units like prey—over a set time. These experiments systematically vary prey availability to observe how it affects the consumer's feeding behaviour. The data generated by such experiments are often analysed using differential equation-based models. Here, we argue that such models do not represent a realistic data-generating process for many such experiments and propose an alternative stochastic individual-based model. This class of models, however, is expensive for inference, and we use machine learning methods to expedite fitting these models to data. We then use our method to do generalised linear model-based inference for a series of experiments conducted on a stickleback fish. Our methodology is made available to others in a Python package for Bayesian hierarchical inference for stochastic, individual-based models of functional responses.

How do mobile organisms situate themselves in space?  This is a fundamental question in both ecology and cell biology but, since space use is an emergent feature of movement processes operating on small spatio-temporal scales, it requires a mathematical approach to answer.  In recent years, increasing empirical research has shown that non-locality is a key aspect of movement processes, whilst mathematical models have demonstrated its importance for understanding emergent space use patterns.  In this talk, I will describe a broad class of models for modelling the space use of interacting populations, whereby directed movement is in the form of non-local advection.  I will detail various methods for ascertaining pattern formation properties of these models, fundamental for answering the question of how organisms situate themselves in space, and describe some of the rich variety of patterns that emerge. I will also explain how to connect these models to data on animal and cellular movement.

Recent progress in the development of equivariant neural network architectures predominantly used for machine learning interatomic potentials (MLIPs) has opened new possibilities in the development of data-driven coarse-graining strategies. In this talk, I will first present our work on the development of learning potential energy surfaces and other physical quantities, namely the Hyperactive Learning framework[1], a Bayesian active learning strategy for automatic efficient assembly of training data in MLIP and ACEfriction [2], a framework for equivariant model construction based on the Atomic Cluster Expansion (ACE) for learning of configuration-dependent friction tensors in the dynamic equations of molecule surface interactions and Dissipative Particle Dynamics (DPD). In the second part of my talk, I will provide an overview of our work on the simulation and analysis of Generalized Langevin Equations [3,4] as obtained from systematic coarse-graining of Hamiltonian Systems via a Mori-Zwanzig projection and present an outlook on our ongoing work on developing data-driven approaches for the construction of dynamics-preserving coarse-grained representations.

References:

[1] van der Oord, C., Sachs, M., Kovács, D.P., Ortner, C. and Csányi, G., 2023. Hyperactive learning for data-driven interatomic potentials. npj Computational Materials

[2] Sachs, M., Stark, W.G., Maurer, R.J. and Ortner, C., 2024. Equivariant Representation of Configuration-Dependent Friction Tensors in Langevin Heatbaths. to appear in Machine Learning: Science & Technology

[3] Leimkuhler, B. and Sachs, M., 2022. Efficient numerical algorithms for the generalized Langevin equation. SIAM Journal on Scientific Computing

[4] Leimkuhler, B. and Sachs, M., 2019. Ergodic properties of quasi-Markovian generalized Langevin equations with configuration-dependent noise and non-conservative force. In Stochastic Dynamics Out of Equilibrium: Institut Henri Poincaré, 2017 

The epithelial to mesenchymal transition (EMT) is a key cellular process underlying cancer progression, with multiple intermediate states whose molecular hallmarks remain poorly characterized. In this talk, I will describe AI-powered and ecology-inspired methods recently developed by us to provide a multi-scale view of the epithelial-mesenchymal plasticity in cancer from single cell and spatial transcriptomics data. First, we employed a large language model similar to the one underlying chatGPT but tailored for biological data (inspired by scBERT methodology), to predict individual stable states within the EMT continuum in single cell data and dissect the regulatory processes governing these states. Secondly, we leveraged spatial transcriptomics of breast cancer tissue to delineate the spatial relationships between cancer cells occupying distinct states within the EMT continuum and various hallmarks of the tumour microenvironment. We introduce a new tool, SpottedPy, that identifies tumour hotspots within spatial transcriptomics slides displaying enrichment in processes of interest, including EMT, and explores the distance between these hotspots and immune/stromal-rich regions within the broader environment at flexible scales. We use this method to delineate an immune evasive quasi-mesenchymal niche that could be targeted for therapeutic benefit. Our insights may inform strategies to counter immune evasion enabled by EMT and offer an expanded view of the coupling between EMT and microenvironmental plasticity in breast cancer.

Tumour microenvironment is characterised by heterogeneity at various scales: from various cell populations (immune cells, cancerous cells, ...) and various molecules that populate the microenvironment (cytokines, chemokines, extracellular vesicles, …); to phenotype heterogeneity inside the same cell population (e.g., immune cells with different phenotypes and different functions); as well as temporal heterogeneity in cells’ phenotypes (as cancer evolves through time) and spatial heterogeneity.
In this talk we overview some mathematical models and computational approaches developed to investigate different single-scale and multi-scale aspects related to heterogeneous immune responses during cancer evolution. Throughout the talk we emphasise the qualitative vs. quantitative results, and data availability across different scales

Understanding how living systems dynamically self-organise across spatial and temporal scales is a fundamental problem in biology; from the study of embryo development to regulation of cellular physiology. In this talk, I will discuss how we can use mathematical modelling to uncover the role of microscale physical interactions in cellular self-organisation. I will illustrate this by presenting two seemingly unrelated problems: environmental-driven compartmentalisation of the intracellular space; and self-organisation during collective migration of multicellular communities. Our results reveal hidden connections between these two processes hinting at the general role that chemical regulation of physical interactions plays in controlling self-organisation across scales in living matter

In this talk I will give a number of short vignettes of work that has been undertaken in my group over the last 15 years. Mathematically, the theme that underlies our work is the importance of randomness to biological systems. I will explore a number of systems for which randomness plays a critical role. Models of these systems which ignore this important feature do a poor job of replicating the known biology, which in turn limits their predictive power. The underlying biological theme of the majority our work is development, but the tools and techniques we have built can be applied to multiple biological systems and indeed further afield. Topics will be drawn from, locust migration, zebrafish pigment pattern formation, mammalian cell migratory defects, appropriate cell cycle modelling and more. I won't delve to deeply into anyone area, but am happy to take question or to expand upon of the areas I touch on.

Deep learning algorithms provide unprecedented opportunities to characterise complex structure in large data, but typically in a manner that cannot easily be interpreted beyond the 'black box'. We are developing methods to leverage the benefits of deep generative learning and computational modelling (e.g. fluid dynamics, solid mechanics, biochemistry), particularly in conjunction with biomedical imaging, to enable new insights into disease to be made. In this talk, I will describe our applications in several areas, including modelling drug delivery in cancer and retinal blood vessel loss in diabetes, and how this is leading us into the development of personalised digital twins.

Advances in spatial profiling technologies are providing insights into how molecular programs are influenced by local signalling and environmental cues. However, cell fate specification and tissue patterning involve the interplay of biochemical and mechanical feedback. Here, we propose a new computational framework that enables the joint statistical analysis of transcriptional and mechanical signals in the context of spatial transcriptomics. To illustrate the application and utility of the approach, we use spatial transcriptomics data from the developing mouse embryo to infer the forces acting on individual cells, and use these results to identify mechanical, morphometric, and gene expression signatures that are predictive of tissue compartment boundaries. In addition, we use geoadditive structural equation modelling to identify gene modules that predict the mechanical behaviour of cells in an unbiased manner. This computational framework is easily generalized to other spatial profiling contexts, providing a generic scheme for exploring the interplay of biomolecular and mechanical cues in tissues.

Underlying many biological models are chemical reaction networks (CRNs), and identifying allowed and forbidden dynamics in reaction networks may 
give insight into biological mechanisms. Algebraic approaches have been important in several recent developments. For example, computational 
algebra has helped us characterise all small mass action CRNs admitting certain bifurcations; allowed us to find interesting and surprising 
examples and counterexamples; and suggested a number of conjectures.   Progress generally involves an interaction between analysis and 
computation: on the one hand, theorems which recast apparently difficult questions about dynamics as (relatively tractable) algebraic problems; 
and on the other, computations which provide insight into deeper theoretical questions. I'll present some results, examples, and open 
questions, focussing on two domains of CRN theory: the study of local bifurcations, and the study of multistationarity.

Understanding the mechanisms behind the spatial distribution, self-organisation and aggregation of organisms is a central issue in both ecology and cell biology. Since self-organisation at the population level is the cumulative effect of behaviours at the individual level, it requires a mathematical approach to be elucidated.
In nature, every individual, be it a cell or an animal, inspects its territory before moving. The process of acquiring information from the environment is typically non-local, i.e. individuals have the ability to inspect a portion of their territory. In recent years, a growing body of empirical research has shown that non-locality is a key aspect of movement processes, while mathematical models incorporating non-local interactions have received increasing attention for their ability to accurately describe how interactions between individuals and their environment can affect their movement, reproduction rate and well-being. In this talk, I will present a study of a class of advection-diffusion equations that model population movements generated by non-local species interactions. Using a combination of analytical and numerical tools, I will show that these models support a wide variety of spatio-temporal patterns that are able to reproduce segregation, aggregation and time-periodic behaviours commonly observed in real systems. I will also show the existence of parameter regions where multiple stable solutions coexist and hysteresis phenomena.
Overall, I will describe various methods for analysing bifurcations and pattern formation properties of these models, which represent an essential mathematical tool for addressing fundamental questions about the many aggregation phenomena observed in nature.
 

We consider a system of interacting particles as a model for a foraging ant colony, where each ant is represented as an active Brownian particle. The interactions among ants are mediated through chemotaxis, aligning their orientations with the upward gradient of a pheromone field. Unlike conventional models, our study introduces a parameter that enables the reproduction of two distinctive behaviours: the conventional Keller-Segel aggregation and the formation of travelling clusters without relying on external constraints such as food sources or nests. We consider the associated mean-field limit of this system and establish the analytical and numerical foundations for understanding these particle behaviours.

Cells must reliably coordinate responses to noisy external stimuli for proper functionality whether deciding where to move or initiate a response to threats. In this talk I will present a perspective on such cellular decision making problems with extreme statistics. The central premise is that when a single stochastic process exhibits large variability (unreliable), the extrema of multiple processes has a remarkably tight distribution (reliable). In this talk I will present some background on extreme statistics followed by two applications. The first regards antigen discrimination - the recognition by the T cell receptor of foreign antigen. The second concerns directional sensing - the process in which cells acquire a direction to move towards a target. In both cases, we find that extreme statistics explains how cells can make accurate and rapid decisions, and importantly, before any steady state is reached.

Turing patterns have long been proposed as a mechanism for spatial organization in biology, but their relevance remains controversial due to the stringent fine-tuning often required. In this talk, I will present recent efforts to engineer synthetic Turing systems in bacterial colonies, highlighting both successes and limitations. While our three-node gene circuit generates patterns, challenges remain in extending these results to broader contexts. Additionally, I will discuss our exploration of machine learning methods to address the inverse problem of pattern formation, helping the design process down the road. This work addresses the ongoing task in translating theory into robust biological applications, offering insights into both current capabilities and future directions.

Immunological health relies on a balance between the ability to mount an immune response against potential pathogens and tolerance to self. However, how we keep that balance in health and what goes wrong in disease is not well understood. Here, I will describe combination of novel experimental and computational approaches using multi-omics datasets, imaging and functional experiments to dissect the role and defects in immune cells across several disease areas in cancer and autoimmunity. We show how shared mechanisms that are disrupted across diseases, including cellular, migration, immuno-surveillance, regulation and activation, as well as the immunological features associated with better prognosis and immunomodulation.

In this talk, I will describe some of the ways in which mathematical modelling contributed to the Covid-19 pandemic response in New Zealand. New Zealand adopted an elimination strategy at the beginning of the pandemic and used a combination of public health measures and border restrictions to keep incidence of Covid-19 low until high vaccination rates were achieved. The low or zero prevalence for first 18 months of the pandemic called for a different set of modelling tools compared to high-prevalence settings. It also generated some unique data that can give valuable insights into epidemiological characteristics and dynamics. As well as describing some of the modelling approaches used, I will reflect on the value modelling can add to decision making and some of the challenges and opportunities in working with stakeholders in government and public health.        

In this presentation, we will review how the field of Mechanics of Materials is generally framed and see how it can benefit from and be of benefit to the current progress in AI. We will approach this problematic in the particular context of Brain mechanics with an application to traumatic brain injury in police investigations. Finally we will briefly show how our group is currently applying the same methodology to a range of engineering challenges.

Morphogen protein gradients play an essential role in the spatial regulation of patterning during embryonic development.  The most commonly accepted mechanism of protein gradient formation involves the diffusion and degradation of morphogens from a localized source. Recently, an alternative mechanism has been proposed, which is based on cell-to-cell transport via thin, actin-rich cellular extensions known as cytonemes. It has been hypothesized that cytonemes find their targets via a random search process based on alternating periods of retraction and growth, perhaps mediated by some chemoattractant. This is an actin-based analog of the search-and-capture model of microtubules of the mitotic spindle searching for cytochrome binding sites (kinetochores) prior to separation of cytochrome pairs. In this talk, we introduce a search-and-capture model of cytoneme-based morphogenesis, in which nucleating cytonemes from a source cell dynamically grow and shrink until making contact with a target cell and delivering a burst of morphogen. We model the latter as a one-dimensional search process with stochastic resetting, finite returns times and refractory periods. We use a renewal method to calculate the splitting probabilities and conditional mean first passage times (MFPTs) for the cytoneme to be captured by a given target cell. We show how multiple rounds of search-and-capture, morphogen delivery, cytoneme retraction and nucleation events lead to the formation of a morphogen gradient. We proceed by formulating the morphogen bursting model as a queuing process, analogous to the study of translational bursting in gene networks. We end by briefly discussing current work on a model of cytoneme-mediated within-host viral spread.

In this talk I will discuss how phenotypic heterogeneity affects emergent pattern formation in living active matter with chemical communication between cells. In doing so, I will explore how the emergent dynamics of multicellular communities are qualitatively different in comparison to the dynamics of isolated or non-interacting cells. I will focus on two specific projects. First, I will show how genetic regulation of chemical communication affects motility-induced phase separation in cell populations. Second, I will demonstrate how chemotaxis along self-generated signal gradients affects cell populations undergoing 3D morphogenesis.

The role of tissue stiffness in controlling cell behaviours ranging from proliferation to signalling and activation is by now well accepted. A key focus of experimental studies into mechanotransduction are focal adhesions, localised patches of strong adhesion, where cell signalling has been established to occur. However, these adhesion sites themselves alter the mechanical equilibrium of the system determining the force balance and work done. To explore this I have developed an active matter continuum description of cellular contractility and will discuss recent results on the specific role of spatial positioning of adhesions in mechanotransduction. I show using energy arguments why the experimentally observed arrangements of focal adhesions develop and the implications this has for stiffness sensing and cellular contractility control. I will also show how adhesions play distinct roles in single cells and tissue layers respectively drawing on recent experimental work with Dr JR Davis (Manchester University) and Dr Nic Tapon (Crick Institute) with applications to epithelial layers and organoids.