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Body size drives the energetic demands of organisms, constraining trophic interactions between species and playing a significant role in shaping the feasibility of species' populations in a community. On macroevolutionary timescales, these demands feed back to shape the selective landscape driving the evolution of body size and diet. We develop a theoretical framework for a three-level trophic food chain -- typical for terrestrial mammalian ecosystems -- premised on bioenergetic trade-offs to explore mammalian population dynamics. Our results show that interactions between predators, prey, and external subsidies generate instabilities linked to body size extrema, corresponding to observed limits of predator size and diet. These instabilities generate size-dependent constraints on coexistence and highlight a feasibility range for carnivore size between 40 to 110 kg, encompassing the mean body size of terrestrial Cenozoic hypercarnivores. Finally, we show that predator dietary generalization confers a selective advantage to larger carnivores, which then declines at megapredator body sizes, aligning with diet breadth estimates for contemporary and Pleistocene species. Our framework underscores the importance of understanding macroevolutionary constraints through the lens of ecological pressures, where the selective forces shaping and reshaping the dynamics of communities can be explored., Comment: 14 pages, 3 figures, SI Appendices

Regulatory functions are essential in both socioeconomic and biological systems, from corporate managers to regulatory genes in genomes. Regulatory functions come with substantial costs, but are often taken for granted. Here, we empirically examine regulatory costs across diverse systems -- biological organisms (bacteria and eukaryotic genomes), human organizations (companies, federal agencies, universities), and decentralized entities (Wikipedia, cities) -- using scaling analysis. We guide the empirical analysis with a conceptual model, which anticipates the scaling of regulatory costs to shift with the system's internal interaction structure -- well-mixed or modular. We find diverse systems exhibit consistent scaling patterns -- well-mixed systems exhibit superlinear scaling, while modular ones show sublinear or linear scaling. Further, we find that the socioeconomic systems containing more diverse occupational functions tend to have more regulatory costs than expected from their size, confirming the type of interactions also plays a role in regulatory costs. While many socioeconomic systems exhibit efficiencies of scale, regulatory costs in many social systems have grown disproportionally over time. Our finding suggests that the increasing complexity of functions may contribute to this trend. This cross-system comparison offers a framework for understanding regulatory costs and could guide future efforts to identify and mitigate regulatory inefficiencies., Comment: 12 pages, 4 figures

Many physical, biological, and even social systems are faced with the problem of how to efficiently harvest free energy from an environment that can have many possible states, yet only have a limited number of harvesting protocols to choose among. We investigate this scenario by extending earlier work on using feedback control to extract work from nonequilibirum systems. Specifically, in contrast to that previous work on the thermodynamics of feedback control, we analyze the combined and separate effects of noisy measurements, memory limitations, and limitations on the number of possible work extraction protocols. Our analysis provides a general recipe to construct repertoires of allowed harvesting protocols that minimize the expected thermodynamic losses during free energy harvesting, i.e., that minimize expected entropy production. In particular, our results highlight that the benefits of feedback control over uninformed (random) actions extend beyond just the associated information gain, often by many orders of magnitude. Our results also uncover the effects of limitations on the number of possible harvesting protocols when there is uncertainty about the distribution over states of the environment., Comment: V2: Extended results and improved presentation. Updated Introduction and Figure 1, added Figures 2 and 3, added Appendices C and D, added Table I. 20 pages, 3 figures

Assembly theory (AT) quantifies selection using the assembly equation and identifies complex objects that occur in abundance based on two measurements, assembly index and copy number, where the assembly index is the minimum number of joining operations necessary to construct an object from basic parts, and the copy number is how many instances of the given object(s) are observed. Together these define a quantity, called Assembly, which captures the amount of causation required to produce objects in abundance in an observed sample. This contrasts with the random generation of objects. Herein we describe how AT's focus on selection as the mechanism for generating complexity offers a distinct approach, and answers different questions, than computational complexity theory with its focus on minimum descriptions via compressibility. To explore formal differences between the two approaches, we show several simple and explicit mathematical examples demonstrating that the assembly index, itself only one piece of the theoretical framework of AT, is formally not equivalent to other commonly used complexity measures from computer science and information theory including Shannon entropy, Huffman encoding, and Lempel-Ziv-Welch compression. We also include proofs that assembly index is not in the same computational complexity class as these compression algorithms and discuss fundamental differences in the ontological basis of AT, and assembly index as a physical observable, which distinguish it from theoretical approaches to formalizing life that are unmoored from measurement., Comment: 38 pages, 4 figures, 1 table, and 91 references plus supplement with proof of assembly index computational class

Metabolic scaling is one of the most important patterns in biology. Theory explaining the 3/4-power size-scaling of biological metabolic rate does not predict the non-linear scaling observed for smaller life forms. Here we present a new model for cells $<10^{-8}$ m$^{3}$ that maximizes power from the reaction-displacement dynamics of enzyme-catalyzed reactions. Maximum metabolic rate is achieved through an allocation of cell volume to optimize a ratio of reaction velocity to molecular movement. Small cells $< 10^{-17}$ m$^{3}$ generate power under diffusion by diluting enzyme concentration as cell volume increases. Larger cells require bulk flow of cytoplasm generated by molecular motors. These outcomes predict curves with literature-reported parameters that match the observed scaling of metabolic rates for unicells, and predicts the volume at which Prokaryotes transition to Eukaryotes. We thus reveal multiple size-dependent physical constraints for microbes in a model that extends prior work to provide a parsimonious hypothesis for how metabolism scales across small life., Comment: 22 pages, 6 figures

Cloud computing offers an opportunity to run compute-resource intensive climate models at scale by parallelising model runs such that datasets useful to the exoplanet community can be produced efficiently. To better understand the statistical distributions and properties of potentially habitable planetary atmospheres we implemented a parallelised climate modelling tool to scan a range of hypothetical atmospheres.Starting with a modern day Earth atmosphere, we iteratively and incrementally simulated a range of atmospheres to infer the landscape of the multi-parameter space, such as the abundances of biological mediated gases (\ce{O2}, \ce{CO2}, \ce{H2O}, \ce{CH4}, \ce{H2}, and \ce{N2}) that would yield `steady state' planetary atmospheres on Earth-like planets around solar-type stars. Our current datasets comprises of \numatmospheres simulated models of exoplanet atmospheres and is available publicly on the NASA Exoplanet Archive. Our scalable approach of analysing atmospheres could also help interpret future observations of planetary atmospheres by providing estimates of atmospheric gas fluxes and temperatures as a function of altitude. Such data could enable high-throughput first-order assessment of the potential habitability of exoplanetary surfaces and sepcan be a learning dataset for machine learning applications in the atmospheric and exoplanet science domain., Comment: 9 pages, 6 figures

Autocatalysis is thought to have played an important role in the earliest stages of the origin of life. An autocatalytic cycle (AC) is a set of reactions that results in stoichiometric increase in its constituent chemicals. When the reactions of multiple interacting ACs are active in a region of space, they can have interactions analogous to those between species in biological ecosystems. Prior studies of autocatalytic chemical ecosystems (ACEs) have suggested avenues for accumulating complexity, such as ecological succession, as well as obstacles such as competitive exclusion. We extend this ecological framework to investigate the effects of surface adsorption, desorption, and diffusion on ACE ecology. Simulating ACEs as particle-based stochastic reaction-diffusion systems in spatial environments-including open, two-dimensional reaction-diffusion systems and adsorptive mineral surfaces-we demonstrate that spatial structure can enhance ACE diversity by i) permitting otherwise mutually exclusive ACs to coexist and ii) subjecting new AC traits to selection.

Energy flow through consumer-resource interactions is largely determined by body size. Allometric relationships govern the dynamics of populations by impacting rates of reproduction, as well as alternative sources of mortality, which have differential impacts on smaller to larger organisms. Here we derive and investigate the timescales associated with four alternative sources of mortality for terrestrial mammals: mortality from starvation, mortality associated with aging, mortality from consumption by predators, and mortality introduced by anthropogenic subsidized harvest. The incorporation of these allometric relationships into a minimal consumer-resource model illuminates central constraints that may contribute to the structure of mammalian communities. Our framework reveals that while starvation largely impacts smaller-bodied species, the allometry of senescence is expected to be more difficult to observe. In contrast, external predation and subsidized harvest have greater impacts on the populations of larger-bodied species. Moreover, the inclusion of predation mortality reveals mass thresholds for mammalian herbivores, where dynamic instabilities may limit the feasibility of megafaunal populations. We show how these thresholds vary with alternative predator-prey mass relationships, which are not well understood within terrestrial systems. Finally, we use our framework to predict the harvest pressure required to induce mass-specific extinctions, which closely align with previous estimates of anthropogenic megafaunal exploitation in both paleontological and historical contexts. Together our results underscore the tenuous nature of megafaunal populations, and how different sources of mortality may contribute to their ephemeral nature over evolutionary time., Comment: 10 pages, 5 figures, 1 table, 4 appendices, 8 supplementary figures

The search for life beyond the Earth is the overarching goal of the NASA Astrobiology Program, and it underpins the science of missions that explore the environments of Solar System planets and exoplanets. However, the detection of extraterrestrial life, in our Solar System and beyond, is sufficiently challenging that it is likely that multiple measurements and approaches, spanning disciplines and missions, will be needed to make a convincing claim. Life detection will therefore not be an instantaneous process, and it is unlikely to be unambiguous-yet it is a high-stakes scientific achievement that will garner an enormous amount of public interest. Current and upcoming research efforts and missions aimed at detecting past and extant life could be supported by a consensus framework to plan for, assess and discuss life detection claims (c.f. Green et al., 2021). Such a framework could help increase the robustness of biosignature detection and interpretation, and improve communication with the scientific community and the public. In response to this need, and the call to the community to develop a confidence scale for standards of evidence for biosignature detection (Green et al., 2021), a community-organized workshop was held on July 19-22, 2021. The meeting was designed in a fully virtual (flipped) format. Preparatory materials including readings, instructional videos and activities were made available prior to the workshop, allowing the workshop schedule to be fully dedicated to active community discussion and prompted writing sessions. To maximize global interaction, the discussion components of the workshop were held during business hours in three different time zones, Asia/Pacific, European and US, with daily information hand-off between group organizers., Comment: 86 pages, 14 figures, workshop report

The production of waste as a consequence of human activities is one of the most fundamental challenges facing our society and global ecological systems. Waste generation is rapidly increasing, with corresponding shifts in the structure of our societies where almost all nations are moving from rural agrarian societies to urban and technological ones. However, the connections between these radical societal shifts and waste generation have not yet been described. Here we apply scaling theory to establish a new understanding of waste in urban systems. We identify universal scaling laws of waste generation across diverse urban systems worldwide for three forms of waste: wastewater, municipal solid waste, and greenhouse gasses. We show that wastewater generation scales superlinearly, municipal solid waste scales linearly, and greenhouse gasses scales sublinearly with city size. In specific cases production can be understood in terms of city size coupled with financial and natural resources. For example, wastewater generation can be understood in terms of the increased economic activity of larger cities, and the deviations around the scaling relationship - indicating relative efficiency - depend on GDP per person and local rainfall. We also show how the temporal evolution of these scaling relationships reveals a loss of economies of scale and the general increase in waste production, where sublinear scaling relationships become linear. Our findings suggest general mechanisms controlling waste generation across diverse cities and global urban systems. Our approach offers a systematic approach to uncover these underlying mechanisms that might be key to reducing waste and pursing a more sustainable future.

Function diversity, namely, the range of tasks individuals can perform, is essential to productive organizations. This concept has been studied in disparate discipline contexts, while general patterns and mechanisms remain unclear. Here, we first analyze over five thousand observations of top-down organizations -- US federal agencies, Norwegian companies, and US universities, and find that the number of distinct functions scales with organizational size, approximately as a power law with an exponent of 1/2. Further, we find common patterns in the distribution of function abundance within organizations. This universality suggests that human organizations, despite differences in their purpose, structure, and culture, may share common mechanisms for creating specializations. Additionally, we find that cities -- bottom-up organizations -- differ from top-down organizations and exhibit logarithmic scaling. We discuss potential avenues for modeling the mechanisms for these observations using history-dependent random processes, and offer several criteria for model selection., Comment: 13 pages, 3 figures

Since the time of Darwin, scientists have struggled to reconcile the evolution of biological forms in a universe determined by fixed laws. These laws underpin the origin of life, evolution, human culture and technology, as set by the boundary conditions of the universe, however these laws cannot predict the emergence of these things. By contrast evolutionary theory works in the opposite direction, indicating how selection can explain why some things exist and not others. To understand how open-ended forms can emerge in a forward-process from physics that does not include their design, a new approach to understand the non-biological to biological transition is necessary. Herein, we present a new theory, Assembly Theory (AT), which explains and quantifies the emergence of selection and evolution. In AT, the complexity of an individual observable object is measured by its Assembly Index (a), defined as the minimal number of steps needed to construct the object from basic building blocks. Combining a with the copy number defines a new quantity called Assembly which quantifies the amount of selection required to produce a given ensemble of objects. We investigate the internal structure and properties of assembly space and quantify the dynamics of undirected exploratory processes as compared to the directed processes that emerge from selection. The implementation of assembly theory allows the emergence of selection in physical systems to be quantified at any scale as the transition from undirected-discovery dynamics to a selected process within the assembly space. This yields a mechanism for the onset of selection and evolution and a formal approach to defining life. Because the assembly of an object is easily calculable and measurable it is possible to quantify a lower limit on the amount of selection and memory required to produce complexity uniquely linked to biology in the universe., Comment: 22 pages, 7 figures

Enabling widespread electric vehicle (EV) adoption requires substantial build-out of charging infrastructure in the coming decade. We formulate the charging infrastructure needs as a scaling analysis problem and use it to estimate the EV infrastructure needs of the US at a county-level resolution. Surprisingly, we find that the current EV infrastructure deployment scales super-linearly with population, deviating from the sub-linear scaling of gasoline stations and other infrastructure. We discuss how this demonstrates the infancy of EV station abundance compared to other mature transportation infrastructures. By considering the power delivery of existing gasoline stations, and appropriate EV efficiencies, we estimate the EV infrastructure gap at the county level, providing a road map for future EV infrastructure expansion. Our reliance on scaling analysis allows us to make a unique forecast in this domain., Comment: 3 pages, 3 figures, 1 table

Innovation and obsolescence describe dynamics of ever-churning and adapting social and biological systems, concepts that encompass field-specific formulations. We formalize the connection with a reduced model of the dynamics of the "space of the possible" (e.g. technologies, mutations, theories) to which agents (e.g. firms, organisms, scientists) couple as they grow, die, and replicate. We predict three regimes: the space is finite, ever growing, or a Schumpeterian dystopia in which obsolescence drives the system to collapse. We reveal a critical boundary at which the space of the possible fluctuates dramatically in size, displaying recurrent periods of minimal and of veritable diversity. When the space is finite, corresponding to physically realizable systems, we find surprising structure. This structure predicts a taxonomy for the density of agents near and away from the innovative frontier that we compare with distributions of firm productivity, covid diversity, and citation rates for scientific publications. Remarkably, our minimal model derived from first principles aligns with empirical examples, implying a follow-the-leader dynamic in firm cost efficiency and biological evolution, whereas scientific progress reflects consensus that waits on old ideas to go obsolete. Our theory introduces a fresh and empirically testable framework for unifying innovation and obsolescence across fields.

Publicly traded companies are fundamental units of contemporary economies and markets and are important mechanisms through which humans interact with their environments. Understanding the general properties that underlie the processes of their growth has long been of interest, yet fundamental debates about the effects of firm size on growth have persisted. Here we develop a scaling framework that focuses on company size as the critical feature determining a variety of tradeoffs, and use this to reveal novel systematic behavior across the diversity of publicly-traded companies. Using a large database of 31,553 US companies over nearly 70 years, and 3,160 Chinese companies over 24 year, we show how the dynamics of companies expressed as scaling relationships leads to a quantitative, analytic theory for their growth. This theory produces several predictions that are in good agreement with data for both the US and China, whose markets have strikingly different histories and underlying structures. In both cases sales scale sublinearly with assets and exhibit nearly identical exponents leading, surprisingly and nontrivially, to assets that grow as a power law in time rather than exponentially, as often assumed. On the other hand, liabilities scale linearly in the US (exponent of $1.0$) but superlinearly in China (exponent of $1.09$). We show that such small differences in scaling exponents can have a significant impact on the character and long-term evolution of growth trajectories. These results illustrate that while companies are part of a larger class of growth phenomena driven by incomes and costs that scale with size, they are unique in that they grow following a temporal power-function which sets them apart from organisms, cities, nations, and markets, whose growth over time is often exponential., Comment: 17 pages, 6 figures, 1 table; revised version

Urban scaling analysis, the study of how aggregated urban features vary with the population of an urban area, provides a promising framework for discovering commonalities across cities and uncovering dynamics shared by cities across time and space. Here, we use the urban scaling framework to study an important, but under-explored feature in this community - income inequality. We propose a new method to study the scaling of income distributions by analyzing total income scaling in population percentiles. We show that income in the least wealthy decile (10%) scales close to linearly with city population, while income in the most wealthy decile scale with a significantly superlinear exponent. In contrast to the superlinear scaling of total income with city population, this decile scaling illustrates that the benefits of larger cities are increasingly unequally distributed. For the poorest income deciles, cities have no positive effect over the null expectation of a linear increase. We repeat our analysis after adjusting income by housing cost, and find similar results. We then further analyze the shapes of income distributions. First, we find that mean, variance, skewness, and kurtosis of income distributions all increase with city size. Second, the Kullback-Leibler divergence between a city's income distribution and that of the largest city decreases with city population, suggesting the overall shape of income distribution shifts with city population. As most urban scaling theories consider densifying interactions within cities as the fundamental process leading to the superlinear increase of many features, our results suggest this effect is only seen in the upper deciles of the cities. Our finding encourages future work to consider heterogeneous models of interactions to form a more coherent understanding of urban scaling., Comment: 18 pages, 7 figures

Understanding the cross-species behavior of cancer is important for uncovering fundamental mechanisms of carcinogenesis, and for translating results of model systems between species. One of the most famous interspecific considerations of cancer is Peto's paradox, which asserts that organisms with vastly different body mass are expected to have a vastly different degree of cancer risk, a pattern that is not observed empirically. Here we show that this observation is not a paradox at all but follows naturally from the interspecific scaling of metabolic rates across mammalian body size. We connect metabolic allometry to evolutionary models of cancer development in tissues to show that waiting time to cancer scales with body mass in a similar way as normal organism lifespan does. Thus, the expectation across mammals is that lifetime cancer risk is invariant with body mass. Peto's observation is therefore not a paradox, but the natural expectation from interspecific scaling of metabolism and physiology. These allometric patterns have theoretical implications for understanding life span evolution, and practical implications for using smaller animals as model systems for human cancer., Comment: 10 pages, 3 figures

A central need in the field of astrobiology is generalized perspectives on life that make it possible to differentiate abiotic and biotic chemical systems. A key component of many past and future astrobiological measurements is the elemental ratio of various samples. Classic work on Earth's oceans has shown that life displays a striking regularity in the ratio of elements as originally characterized by Redfield. The body of work since the original observations has connected this ratio with basic ecological dynamics and cell physiology, while also documenting the range of elemental ratios found in a variety of environments. Several key questions remain in considering how to best apply this knowledge to astrobiological contexts: How can the observed variation of the elemental ratios be more formally systematized using basic biological physiology and ecological or environmental dynamics? How can these elemental ratios be generalized beyond the life that we have observed on our own planet? Here we expand recently developed generalized physiological models to create a simple framework for predicting the variation of elemental ratios found in various environments. We then discuss further generalizing the physiology for astrobiological applications. Much of our theoretical treatment is designed for in situ measurements applicable to future planetary missions. We imagine scenarios where three measurements can be made - particle/cell sizes, particle/cell stoichiometry, and fluid or environmental stoichiometry - and develop our theory in connection with these often deployed measurements., Comment: 18 pages, 5 figures

Population-level scaling in ecological systems arises from individual growth and death with competitive constraints. We build on a minimal dynamical model of metabolic growth where the tension between individual growth and mortality determines population size distribution. We include resource competition based on shared capture area separately. By varying relative rates of growth, death, and competitive attrition, we connect regular and random spatial patterns across sessile organisms from forests to ants, termites, and fairy circles. Then, we consider transient temporal dynamics in the context of asymmetric competition that primarily weakens the smaller of two competitors such as canopy shading or large colony dominance. When such competition couples slow timescales of growth with fast competitive death, it generates population shock waves similar to those observed in forest demographic data. Our minimal quantitative theory unifies spatiotemporal patterns across sessile organisms through local competition mediated by the laws of metabolic growth which in turn result from long-term evolutionary dynamics.

The growing need for affordable and accessible higher education is a major global challenge for the 21st century. Consequently, there is a need to develop a deeper understanding of the functionality and taxonomy of universities and colleges and, in particular, how their various characteristics change with size. Scaling has been a powerful tool for revealing systematic regularities in systems across a range of topics from physics and biology to cities, and for understanding the underlying principles of their organization and growth. Here, we apply this framework to institutions of higher learning in the United States and show that, like organisms, ecosystems and cities, they scale in a surprisingly systematic fashion following simple power law behavior. We analyze the entire spectrum encompassing 5,802 institutions ranging from large research universities to small professional schools, organized in seven commonly used sectors, which reveal distinct regimes of institutional scaling behavior. Metrics include variation in expenditures, revenues, graduation rates and estimated economic added value, expressed as functions of total enrollment, our fundamental measure of size. Our results quantify how each regime of institution leverages specific economies of scale to address distinct priorities. Taken together, the scaling of features within a sector and shifts in scaling across sectors implies that there are generic mechanisms and constraints shared by all sectors which lead to tradeoffs between their different societal functions and roles. We particularly highlight the strong complementarity between public and private research universities, and community and state colleges, four sectors that display superlinear returns to scale.

Consumers face numerous risks that can be minimized by incorporating different life-history strategies. How much and when a consumer adds to its energetic reserves or invests in reproduction are key behavioral and physiological adaptations that structure much of how organisms interact. Here we develop a theoretical framework that explicitly accounts for stochastic fluctuations of an individual consumer's energetic reserves while foraging and reproducing on a landscape with resources that range from uniformly distributed to highly clustered. First, we show that optimal life-history strategies vary in response to changes in the mean productivity of the resource landscape, where depleted environments promote reproduction at lower energetic states, greater investment in each reproduction event, and smaller litter sizes. We then show that if resource variance scales with body size due to landscape clustering, consumers that forage for clustered foods are susceptible to strong Allee effects, increasing extinction risk. Finally, we show that the proposed relationship between consumer body size, resource clustering, and Allee effect-induced population instability offers key ecological insights into the evolution of large-bodied grazing herbivores from small-bodied browsing ancestors., Comment: 9 pages, 5 figures, 3 Supplementary Appendices, 2 Supplementary Figures

Biological organisms must perform computation as they grow, reproduce, and evolve. Moreover, ever since Landauer's bound was proposed it has been known that all computation has some thermodynamic cost -- and that the same computation can be achieved with greater or smaller thermodynamic cost depending on how it is implemented. Accordingly an important issue concerning the evolution of life is assessing the thermodynamic efficiency of the computations performed by organisms. This issue is interesting both from the perspective of how close life has come to maximally efficient computation (presumably under the pressure of natural selection), and from the practical perspective of what efficiencies we might hope that engineered biological computers might achieve, especially in comparison with current computational systems. Here we show that the computational efficiency of translation, defined as free energy expended per amino acid operation, outperforms the best supercomputers by several orders of magnitude, and is only about an order of magnitude worse than the Landauer bound. However this efficiency depends strongly on the size and architecture of the cell in question. In particular, we show that the {\it useful} efficiency of an amino acid operation, defined as the bulk energy per amino acid polymerization, decreases for increasing bacterial size and converges to the polymerization cost of the ribosome. This cost of the largest bacteria does not change in cells as we progress through the major evolutionary shifts to both single and multicellular eukaryotes. However, the rates of total computation per unit mass are nonmonotonic in bacteria with increasing cell size, and also change across different biological architectures including the shift from unicellular to multicellular eukaryotes., Comment: 31 pages, 7 figures, 1 Table

World record setting has long attracted public interest and scientific investigation. Extremal records summarize the limits of the space explored by a process, and the historical progression of a record sheds light on the underlying dynamics of the process. Existing analyses of prediction, statistical properties, and ultimate limits of record progressions have focused on particular domains. However, a broad perspective on how record progressions vary across different spheres of activity needs further development. Here we employ cross-cutting metrics to compare records across a variety of domains, including sports, games, biological evolution, and technological development. We find that these domains exhibit characteristic statistical signatures in terms of rates of improvement, "burstiness" of record-breaking time series, and the acceleration of the record breaking process. Specifically, sports and games exhibit the slowest rate of improvement and a wide range of rates of "burstiness." Technology improves at a much faster rate and, unlike other domains, tends to show acceleration in records. Many biological and technological processes are characterized by constant rates of improvement, showing less burstiness than sports and games. It is important to understand how these statistical properties of record progression emerge from the underlying dynamics. Towards this end, we conduct a detailed analysis of a particular record-setting event: elite marathon running. In this domain, we find that studying record-setting data alone can obscure many of the structural properties of the underlying process. The marathon study also illustrates how some of the standard statistical assumptions underlying record progression models may be inappropriate or commonly violated in real-world datasets., Comment: This paper was produced, from conception of idea, to execution, to writing, by a team in just 72 hours (see Appendix)

The eco-evolutionary dynamics of species are fundamentally linked to the energetic constraints of its constituent individuals. Of particular importance is the interplay between reproduction and the dynamics of starvation and recovery. To elucidate this interplay, we introduce a nutritional state-structured model that incorporates two classes of consumer: nutritionally replete, reproducing consumers, and undernourished, non-reproducing consumers. We obtain strong constraints on starvation and recovery rates by deriving allometric scaling relationships and find that population dynamics are typically driven to a steady state. Moreover, these rates fall within a 'refuge' in parameter space, where the probability of population extinction is minimized. We also show that our model provides a natural framework to predict maximum mammalian body size by determining the relative stability of an otherwise homogeneous population to a competing population with altered percent body fat. This framework provides a principled mechanism for a selective driver of Cope's rule., Comment: 13 pages, 5 figures, 1 Supplement, 2 Supplementary figures

Pathogens can spread epidemically through populations. Beneficial contagions, such as viruses that enhance host survival or technological innovations that improve quality of life, also have the potential to spread epidemically. How do the dynamics of beneficial biological and social epidemics differ from those of detrimental epidemics? We investigate this question using three theoretical approaches. First, in the context of population genetics, we show that a horizontally-transmissible element that increases fitness, such as viral DNA, spreads superexponentially through a population, more quickly than a beneficial mutation. Second, in the context of behavioral epidemiology, we show that infections that cause increased connectivity lead to superexponential fixation in the population. Third, in the context of dynamic social networks, we find that preferences for increased global infection accelerate spread and produce superexponential fixation, but preferences for local assortativity halt epidemics by disconnecting the infected from the susceptible. We conclude that the dynamics of beneficial biological and social epidemics are characterized by the rapid spread of beneficial elements, which is facilitated in biological systems by horizontal transmission and in social systems by active spreading behavior of infected individuals., Comment: The original version of this paper [v1] was produced, from conception of idea, to execution, to writing, by a team in just 72 hours (see Appendix of [v1]). This is a revised version

In the face of uncertain biological response to climate change and the many critiques concerning model complexity it is increasingly important to develop predictive mechanistic frameworks that capture the dominant features of ecological communities and their dependencies on environmental factors. This is particularly important for critical global processes such as biomass changes, carbon export, and biogenic climate feedback. Past efforts have successfully understood a broad spectrum of plant and community traits across a range of biological diversity and body size, including tree size distributions and maximum tree height, from mechanical, hydrodynamic, and resource constraints. Recently it was shown that global scaling relationships for net primary productivity are correlated with local meteorology and the overall biomass density within a forest. Along with previous efforts, this highlights the connection between widely observed allometric relationships and predictive ecology. An emerging goal of ecological theory is to gain maximum predictive power with the least number of parameters. Here we show that the explicit dependence of such critical quantities can be systematically predicted knowing just the size of the largest tree. This is supported by data showing that forests converge to our predictions as they mature. Since maximum tree size can be calculated from local meteorology this provides a general framework for predicting the generic structure of forests from local environmental parameters thereby addressing a range of critical Earth-system questions., Comment: 26 pages, 4 figures, 1 Table