Evolutionary dynamics are shaped by a variety of fundamental, generic drivers, including spatial structure, ecology, and selection pressure. These drivers impact the trajectory of evolution, and have been hypothesized to influence phylogenetic structure. Here, we set out to assess (1) if spatial structure, ecology, and selection pressure leave detectable signatures in phylogenetic structure, (2) the extent, in particular, to which ecology can be detected and discerned in the presence of spatial structure, and (3) the extent to which these phylogenetic signatures generalize across evolutionary systems. To this end, we analyze phylogenies generated by manipulating spatial structure, ecology, and selection pressure within three computational models of varied scope and sophistication. We find that selection pressure, spatial structure, and ecology have characteristic effects on phylogenetic metrics, although these effects are complex and not always intuitive. Signatures have some consistency across systems when using equivalent taxonomic unit definitions (e.g., individual, genotype, species). Further, we find that sufficiently strong ecology can be detected in the presence of spatial s
Datasets encountered when examining deeper issues in ecology and evolution are often complex. This calls for careful strategies for both model building, model selection, and model averaging. Our paper aims at motivating, exhibiting, and further developing focused model selection criteria. In contexts involving precisely formulated interest parameters, these versions of FIC, the focused information criterion, typically lead to better final precision for the most salient estimates, confidence intervals, etc. as compared to estimators obtained from other selection methods. Our methods are illustrated with real case studies in ecology; one related to bird species abundance and another to the decline in body condition for the Antarctic minke whale.
Ecosystems are among the most interesting and well-studied examples of self-organized complex systems. Community ecology, the study of how species interact with each other and the environment, has a rich tradition. Over the last few years, there has been a growing theoretical and experimental interest in these problems from the physics and quantitative biology communities. Here, we give an overview of community ecology, highlighting the deep connections between ecology and statistical physics. We start by introducing the two classes of mathematical models that have served as the workhorses of community ecology: Consumer Resource Models (CRM) and the generalized Lotka-Volterra models (GLV). We place a special emphasis on graphical methods and general principles. We then review recent works showing a deep and surprising connection between ecological dynamics and constrained optimization. We then shift our focus by analyzing these same models in "high-dimensions" (i.e. in the limit where the number of species and resources in the ecosystem becomes large) and discuss how such complex ecosystems can be analyzed using methods from the statistical physics of disordered systems such as the
We propose a model for the evolutionary ecology of words as one attempt to extend evolutionary game theory and agent-based models by utilizing the rich linguistic expressions of Large Language Models (LLMs). Our model enables the emergence and evolution of diverse and infinite options for interactions among agents. Within the population, each agent possesses a short word (or phrase) generated by an LLM and moves within a spatial environment. When agents become adjacent, the outcome of their interaction is determined by the LLM based on the relationship between their words, with the loser's word being replaced by the winner's. Word mutations, also based on LLM outputs, may occur. We conducted preliminary experiments assuming that ``strong animal species" would survive. The results showed that from an initial population consisting of well-known species, many species emerged both gradually and in a punctuated equilibrium manner. Each trial demonstrated the unique evolution of diverse populations, with one type of large species becoming dominant, such as terrestrial animals, marine life, or extinct species, which were ecologically specialized and adapted ones across diverse extreme hab
We present an example of low-carbon research activity carried out by astrophysicists and focused on ecology and environmental protection, with direct impacts on territories and society. This project serves as an illustration of action research for an astrophysics lab in the context of the current ecological crisis.
The surging demand for new energy vehicles is driven by the imperative to conserve energy, reduce emissions, and enhance the ecological ambiance. By conducting behavioral analysis and mining usage patterns of new energy vehicles, particular patterns can be identified. For instance, overloading the battery, operating with low battery power, and driving at excessive speeds can all detrimentally affect the battery's performance. To assess the impact of such driving behavior on the urban ecology, an environmental computational modeling method has been proposed to simulate the interaction between new energy vehicles and the environment. To extend the time series data of the vehicle's entire life cycle and the ecological environment within the model sequence data, the LSTM model with Bayesian optimizer is utilized for simulation. The analysis revealed the detrimental effects of poor driving behavior on the environment.
Due to the heterogeneity of the global distribution of ecological and hydrological ground-truth observations, machine learning models can have limited adaptability when applied to unknown locations, which is referred to as weak extrapolability. Domain adaptation techniques have been widely used in machine learning domains such as image classification, which can improve the model generalization ability by adjusting the difference or inconsistency of the domain distribution between the training and test sets. However, this approach has rarely been used explicitly in machine learning models in ecology and hydrology at the global scale, although these models have often been questioned due to geographic extrapolability issues. This paper briefly describes the shortcomings of current machine learning models of ecology and hydrology in terms of the global representativeness of the distribution of observations and the resulting limitations of the lack of extrapolability and suggests that future related modelling efforts should consider the use of domain adaptation techniques to improve extrapolability.
New technologies for acquiring biological information such as eDNA, acoustic or optical sensors, make it possible to generate spatial community observations at unprecedented scales. The potential of these novel community data to standardize community observations at high spatial, temporal, and taxonomic resolution and at large spatial scale ('many rows and many columns') has been widely discussed, but so far, there has been little integration of these data with ecological models and theory. Here, we review these developments and highlight emerging solutions, focusing on statistical methods for analyzing novel community data, in particular joint species distribution models; the new ecological questions that can be answered with these data; and the potential implications of these developments for policy and conservation.
Increasing attention has been drawn to the misuse of statistical methods over recent years, with particular concern about the prevalence of practices such as poor experimental design, cherry-picking and inadequate reporting. These failures are largely unintentional and no more common in ecology than in other scientific disciplines, with many of them easily remedied given the right guidance. Originating from a discussion at the 2020 International Statistical Ecology Conference, we show how ecologists can build their research following four guiding principles for impactful statistical research practices: 1. Define a focused research question, then plan sampling and analysis to answer it; 2. Develop a model that accounts for the distribution and dependence of your data; 3. Emphasise effect sizes to replace statistical significance with ecological relevance; 4. Report your methods and findings in sufficient detail so that your research is valid and reproducible. Listed in approximate order of importance, these principles provide a framework for experimental design and reporting that guards against unsound practices. Starting with a well-defined research question allows researchers to c
Network ecologists investigate the structure, function, and evolution of ecological systems using network models and analyses. For example, network techniques have been used to study community interactions (i.e., food-webs, mutualisms), gene flow across landscapes, and the sociality of individuals in populations. The work presented here uses a bibliographic and network approach to (1) document the rise of Network Ecology, (2) identify the diversity of topics addressed in the field, and (3) map the structure of scientific collaboration among contributing scientists. Our aim is to provide a broad overview of this emergent field that highlights its diversity and to provide a foundation for future advances. To do this, we searched the ISI Web of Science database for ecology publications between 1900 and 2012 using the search terms for research areas of Environmental Sciences & Ecology and Evolutionary Biology and the topic tag ecology. From these records we identified the Network Ecology publications using the topic terms network, graph theory, and web while controlling for the usage of misleading phrases. The resulting corpus entailed 29,513 publications between 1936 and 2012. We
The implementation of deep learning algorithms has brought new perspectives to plankton ecology. Emerging as an alternative approach to established methods, deep learning offers objective schemes to investigate plankton organisms in diverse environments. We provide an overview of deep-learning-based methods including detection and classification of phyto- and zooplankton images, foraging and swimming behaviour analysis, and finally ecological modelling. Deep learning has the potential to speed up the analysis and reduce the human experimental bias, thus enabling data acquisition at relevant temporal and spatial scales with improved reproducibility. We also discuss shortcomings and show how deep learning architectures have evolved to mitigate imprecise readouts. Finally, we suggest opportunities where deep learning is particularly likely to catalyze plankton research. The examples are accompanied by detailed tutorials and code samples that allow readers to apply the methods described in this review to their own data.
Based on a case study on 3D printing, we have been experimenting on the sonification of multidimensional data for peripheral process monitoring. In a previous paper, we tested the effectiveness of a soundscape which combined intentionally incongruous natural and musical sounds. This was based on the hypothesis that auditory stimuli could better stand out from one another if they were less ecologically coherent, thus allowing for better reaction rates to various notifications. In this paper, we follow up on that hypothesis by testing two new acoustic ecologies, each exclusively consisting of either musical or natural sounds. We then run those ecologies through the same dual-task evaluation process as the previous one in order to compare them. The results seem to favor our hypothesis, as the new ecologies were not detected as accurately as the original. Though, the set of natural sounds seemed to be considered less intrusive by testers, and to allow for a better performance at an external primary task. We hope to see this work become part of a much larger corpus of studies, which may eventually provide a more definite answer on the effect of ecological coherence in peripheral soundsc
The growing use of model-selection principles in ecology for statistical inference is underpinned by information criteria (IC) and cross-validation (CV) techniques. Although IC techniques, such as Akaike's Information Criterion, have been historically more popular in ecology, CV is a versatile and increasingly used alternative. CV uses data splitting to estimate model scores based on (out-of-sample) predictive performance, which can be used even when it is not possible to derive a likelihood (e.g., machine learning) or count parameters precisely (e.g., mixed-effects models and penalised regression). Here we provide a primer to understanding and applying CV in ecology. We review commonly applied variants of CV, including approximate methods, and make recommendations for their use based on the statistical context. We explain some important -- but often overlooked -- technical aspects of CV, such as bias correction, estimation uncertainty, score selection, and parsimonious selection rules. We also address misconceptions (and truths) about impediments to the use of CV, including computational cost and ease of implementation, and clarify the relationship between CV and information-theor
Ecology studies biodiversity in its variety and complexity. It describes how species distribute and perform in response to environmental changes. Ecological processes and structures are highly complex and adaptive. In order to quantify emerging ecological patterns and investigate their hidden mechanisms, we need to rely on the simplicity of mathematical language. This becomes especially apparent when dealing with scaling patterns in ecology. Indeed, nearly all of ecological patterns are scale dependent. Such scale dependence hampers our predictive power and creates problems in our inference. This challenge calls for a clear and fundamental understanding of how and why ecological patterns change across scales. As Simon Levin stated in his MacArthur Award lecture, the problem of relating phenomena across scales is the central problem in ecology and other natural sciences. It has become clear that there is currently a drive in ecology and complexity science to develop new quantitative approaches that are suitable for analysing and forecasting patterns of ecological systems. Here I provide a road map for future works on synthesizing the scaling patterns in ecology, aiming (i) to collec
Microbes are often discussed in terms of dichotomies such as copiotrophic/oligotrophic and fast/slow-growing microbes, defined using the characterisation of microbial growth in isolated cultures. The dichotomies are usually qualitative and/or study-specific, sometimes precluding clear-cut results interpretation. We are able to interpret microbial dichotomies as life history strategies by combining ecology theory with Monod curves, a classical laboratory tool of bacterial physiology. Monod curves relate the specific growth rate of a microbe with the concentration of a limiting nutrient, and provide quantities that directly correspond to key ecological parameters in McArthur and Wilsons r/K selection theory, Tilmans resource competition and community structure theory and Grimes triangle of life strategies. The resulting model allows us to reconcile the copiotrophic/oligotrophic and fast/slow-growing dichotomies as different subsamples of a life history strategy triangle that also includes r/K strategists. We analyzed some ecological context by considering the known viable carbon sources for heterotrophic microbes in the framework of community structure theory. This partly explains th
Percolation offers acknowledged models of random media when the relevant medium characteristics can be described as a binary feature. However, when considering habitat modeling in ecology, a natural constraint comes from nearest-neighbor correlations between the suitable/unsuitable states of the spatial units forming the habitat. Such constraints are also relevant in the physics of aggregation where underlying processes may lead to a form of correlated percolation. However, in ecology, the processes leading to habitat correlations are in general not known or very complex. As proposed by Hiebeler [Ecology {\bf 81}, 1629 (2000)], these correlations can be captured in a lattice model by an observable aggregation parameter $q$, supplementing the density $p$ of suitable sites. We investigate this model as an instance of correlated percolation. We analyze the phase diagram of the percolation transition and compute the cluster size distribution, the pair-connectedness function $C(r)$ and the correlation function $g(r)$. We find that while $g(r)$ displays a power-law decrease associated with long-range correlations in a wide domain of parameter values, critical properties are compatible wi
Biological evolution is realised through the same mechanisms of birth and death that underlie change in population density. The deep interdependence between ecology and evolution is well-established, and recent models focus on integrating eco-evolutionary dynamics to demonstrate how ecological and evolutionary processes interact and feed back upon each other. Nevertheless, a gap remains between the logical foundations of ecology and evolution. Population ecology and evolution have fundamental equations that define how the size of a population (ecology) and the average characteristic within a population (evolution) change over time. These fundamental equations are a complete and exact description of change for any closed population, but how they are formally linked remains unclear. We link the fundamental equations of population ecology and evolution with an equation that sums how individual characteristics interact with individual fitness in a population. From this equation, we derive the fundamental equations of population ecology and evolutionary biology (the Price equation). We thereby identify an overlooked bridge between ecology and biological evolution. Our unification formal
May (1974,1976) opened the debate on whether biological populations might exhibit nonlinear dynamics and chaos. However, it has in general been difficult to verify nonlinear dynamics in biological populations. There are many reports concerning problems with this issue and some of them can be traced back to Hassell, Lawton, and May (1976) and Morris (1990). Our objective is not a discussion of the presence of nonlinear dynamics in biological populations. Instead, we analyze whether ecological census data can be used for validating nonlinearities at all. We choose our models and our situation so that as much as possible can be done rigorously with by hand computations. We consider a clearly nonlinear chemostat based model that is isolated. Some noise must be considered, and we choose a minimal approach: Only noise originating from the fact that ecological populations remain finite is considered, cf. Bailey (1964). In ecology, exceptionally long and famous time series are those collected by Nicholson (1954) and Utida (1957). Our judgement is that ecological time series data containing a few hundred data points is exceptionally long.
With increased access to data and the advent of computers, the use of statistical tools and numerical simulations is becoming commonplace for ecologists. These approaches help improve our understanding of ecological phenomena and their underlying mechanisms in increasingly complex environments. However, the development of mathematical and computational tools has made it possible to study high-dimensional problems up to a certain limit. To overcome this issue, quantum computers could be used to study ecological problems on a larger scale by creating new bridges between fields that at first glance appear to be quite different. We introduce the basic concepts needed to understand quantum computers, give an overview of their applications, and discuss their challenges and future opportunities in ecology. Quantum computers will have a significant impact on ecology by improving the power of statistical tools, solve intractable problems in networks, and help understand the dynamics of large systems of interacting species. This innovative computational perspective could redefine our understanding of species interactions, improve predictive modeling of distributions, and optimize conservatio
New observations are opening the possibility of characterising habitable environments in exoplanetary systems, with the recent example of the candidate hycean world K2-18 b. This motivates an exploration of the possible ecological conditions on such planets to better interpret biosignatures as well as understand the nature of potential life. On Earth, the Lotka-Volterra equations have been used to model numerous coupled populations within ecosystems, from interactions between large vertebrates, to systems with multiple microbial species. In this work, we apply the Lotka-Volterra equations to the ecology of habitable exoplanets for the first time, focusing on hycean worlds. We simulate scenarios in a vertical water column with between 1-5 bacterial species that thrive in anoxic environments on Earth, i.e. similar to predicted hycean conditions. We find that a wide range of ecological diversity is possible for microbial populations under hycean conditions. We demonstrate that dominating phototrophic bacteria at the top of a water column out-compete deeper dwelling phototrophic bacteria, analogous to bacterial blooms on Earth. Incorporating microbial viruses (bacteriophages) within ou