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Coblentz, K. E.

Publications and source records attributed to Coblentz, K. E..

10 recordsLinked to original sources

The OS-Prey (Omnibus Study of Prey) database: A compilation of diet records for birds of prey.

MotivationThe diet composition of a predator is a direct reflection of its role in a food web, resulting from interactions with prey species. Raptors (including hawks, owls, and falcons) are ubiquitous predators with diverse diets, yet there is no comprehensive database of raptor diet composition. We present a database of over 3500 raw raptor diet records, compiled from more than 1000 studies and representing 173 raptor species from across the world. Our dataset complements existing qualitative summaries of species diets by compiling thousands of quantitative diet "samples" over time and space to present diet data at a uniquely fine resolution. Main types of variable containedThe database comprises published records of raptor diets from pellets, prey remains, direct or photographic observations, prey DNA, and raptor gut or gullet contents. For each diet, we present the taxonomic identity and amounts of consumed prey. We additionally present various metadata for each diet such as location, habitat, and season. Spatial location and grainThe study incorporates diet records collected worldwide, with each record assigned geographic coordinates corresponding to the location where the diet information was obtained. Time period and grainThe database includes diet records from 1893 to 2025. We report a year for each diet record. Major taxa and level of measurementWe recorded raptor diet at the species level, including raptors from three orders: Strigiformes, Falconiformes and Accipitriformes excluding vultures. Most prey are identified to species, but prey taxonomic level varies depending on the extent to which they could be identified. Software formatDiet records and metadata are provided in two files with comma-separated value (.csv) format.

ecology↗

Simple, universal rules predict trophic interaction strengths

Many drivers of ecological systems exhibit regular scaling relationships, yet the mechanisms explaining these relationships are often unknown. Trophic interaction strengths are no exception, exhibiting scaling relationships with predator and prey traits that lack evolutionary explanations. We propose two rules to explain the scaling of trophic interaction strengths through the relationship between a predators feeding rate and its preys density -- the so-called predator functional response. First, functional responses allow predators to meet their energetic demands when prey are rare. Second, functional responses approach their maxima near the highest prey densities predators experience. We show that equations derived from these rules predict functional response parameters across over 2,100 functional response experiments and make additional predictions such as their allometric scaling. The two rules thereby offer a potential ultimate explanation for the determinants of trophic interaction strengths, revealing ecologically realized constraints to the complex, adaptive nature of functional response evolution.

ecology↗

In defense of the Type I functional response: The frequency and population-dynamic effects of feeding on multiple prey at a time

Ecologists differ in the degree to which they consider the linear Type I functional response to be an unrealistic versus sufficient representation of predator feeding rates. Empiricists tend to consider it unsuitably non-mechanistic and theoreticians tend to consider it necessarily simple. Hollings original rectilinear Type I response is dismissed by satisfying neither desire, with most compromising on the smoothly saturating Type II response for which searching and handling are assumed to be mutually exclusive activities. We derive a "multiple-prey-at-a-time" response and a generalization that includes the Type III to reflect predators that can continue to search when handling an arbitrary number of already-captured prey. The multi-prey model clarifies the empirical relevance of the linear and rectilinear models and the conditions under which linearity can be a mechanistically-reasoned description of predator feeding rates, even when handling times are long. We find support for linearity in 35% of 2,591 compiled empirical datasets and support for the hypothesis that larger predator-prey body-mass ratios permit predators to search while handling greater numbers of prey. Incorporating the multi-prey response into the Rosenzweig-MacArthur population-dynamics model reveals that a non-exclusivity of searching and handling can lead to coexistence states and dynamics that are not anticipated by theory built on the Type I, II, or III response models. In particular, it can lead to bistable fixed-point and limit-cycle dynamics with long-term crawl-by transients between them under conditions where abundance ratios reflect top-heavy food webs and the functional response is linear. We conclude that functional response linearity should not be considered empirically unrealistic but also that more cautious inferences should be drawn in theory presuming the linear Type I to be appropriate.

ecology↗

Heritable intraspecific variation among prey in size and movement interact to shape predation risk and potential natural selection

O_LIPredator and prey traits are important determinants of the outcomes of trophic interactions. In turn, the outcomes of trophic interactions shape the evolution of predator and prey traits. How species traits are likely to respond to selection from trophic interactions depends crucially on whether and how heritable species traits are and their genetic correlations. Of the many traits potentially influencing the outcomes of trophic interactions, body size and movement traits have emerged as universally key traits. Yet, how these traits shape and are shaped by trophic interactions is generally unclear, as few studies have simultaneously measured the impacts of these traits on the outcomes of trophic interactions, their heritability, and their correlations within the same system. C_LIO_LIWe used outcrossed and then clonally propagated lines of the ciliate protist Paramecium caudatum from natural populations to examine variation in morphology and movement behavior, the extent to which this variation was heritable, and how intraspecific differences among lines altered Paramecium susceptibility to predation by the copepod Macrocyclops albidus. C_LIO_LIWe found that the Paramecium lines exhibited heritable variation in body size and movement traits. In contrast to expectations from interspecific allometric relationships, body size and movement speed showed little covariance among clonal lines. The proportion of Paramecium consumed by copepods was positively associated with Paramecium body size and velocity, however, we also found evidence of an interaction such that greater velocities led to greater predation risk for large body-sized paramecia but did not alter predation risk for smaller body-sized paramecia. The proportion of paramecia consumed was not related to copepod body size. These patterns of predation risk and heritable trait variation in paramecia suggest that copepod predation may act as a selective force operating independently on movement and body size and generating the strongest selection against large, high-velocity paramecia. C_LIO_LIOur results illustrate how the interactions between ecology and genetics can shape the potential natural selection on prey traits through the outcomes of trophic interactions. Further simultaneous measures of predation outcomes, traits, and their quantitative genetic characteristics will provide insights into the evolutionary ecology of species interactions and their eco-evolutionary consequences. C_LI

ecology↗

Ecological boundaries and constraints on viable eco-evolutionary pathways

Evolutionary dynamics are subject to constraints ranging from limitations on what is physically possible to limitations on the pathways that evolution can take. One set of evolutionary constraints, known as demographic constraints, constrain what can occur evolutionarily due to the population demographic or population dynamical consequences of evolution leading to conditions that make populations susceptible to extinction. These demographic constraints can limit the strength of selection or rates of environmental change populations can experience while remaining extant and the trait values a population can express. Here we further hypothesize that the population demographic and population dynamical consequences of evolution also can constrain the eco-evolutionary pathways that populations can traverse by defining ecological boundaries represented by areas of likely extinction. We illustrate this process using a model of predator evolution. Our results show that the populations that persist over time tend to be those whose eco-evolutionary dynamics have avoided ecological boundaries representing areas of likely extinction due to stochastic deviations from a deterministic eco-evolutionary expectation. We term this subset of persisting pathways viable eco-evolutionary pathways. The potential existence of ecological boundaries constraining evolutionary pathways has important implications for predicting evolutionary dynamics, interpreting past evolution, and understanding the role of stochasticity and ecological constraints on eco-evolutionary dynamics.

ecology↗

Predator feeding rates may often be unsaturated under typical prey densities

Predator feeding rates (described by their functional response) must saturate at high prey densities. Although thousands of manipulative functional response experiments show feeding rate saturation at high densities under controlled conditions, it is unclear how saturated feeding rates are at natural prey densities. The general degree of feeding rate saturation has important implications for the processes determining feeding rates and how they respond to changes in prey density. To address this, we linked two databases - one of functional response parameters and one on mass-abundance scaling - through prey mass to calculate a feeding rate saturation index. We find that: 1) feeding rates may commonly be unsaturated and 2) the degree of saturation varies with predator and prey taxonomic identities and body sizes, habitat, interaction dimension, and temperature. These results reshape our conceptualization of predator-prey interactions in nature and suggest new research on the ecological and evolutionary implications of unsaturated feeding rates.

ecology↗

Quantifying predator functional responses under field conditions reveals interactive effects of temperature and interference with sex and stage.

O_LIPredator functional responses describe predator feeding rates and are a core component of predator-prey theory. Although originally defined as the relationship between predator feeding rates and prey densities, it is now well known that predator functional responses are shaped by a multitude of factors. Unfortunately, how these factors interact with one another remains unclear, as widely used laboratory methods for measuring functional responses are generally logistically constrained to examining a few factors simultaneously. Furthermore, it is also often unclear whether laboratory derived functional responses translate to field conditions. C_LIO_LIOur goal was to apply an observational approach for measuring functional responses to understand how sex/stage differences, temperature, and predator interference interact to influence the functional response of zebra jumping spiders on midges under natural conditions. C_LIO_LIWe used field feeding surveys of jumping spiders to infer spider functional responses. We applied a Bayesian model averaging approach to estimate differences among sexes and stages of jumping spiders in their feeding rates and their dependencies on midge densities, temperature, and predator interference. C_LIO_LIWe find that females exhibit the steepest functional responses on midges, followed by juveniles, and then males, despite males being larger than juveniles. We also find that sexes and stages differ in the temperature dependence of their space clearance (aka attack) rates. We find little evidence of temperature dependence in females, whereas we find some evidence for an increase in space clearance rate at high temperatures in males and juveniles. Interference effects on feeding rates were asymmetric with little effect of interference on male feeding rates, and effects of interference on females and juveniles depending on the stage/sex from which the interference originates. C_LIO_LIOur results illustrate the multidimensional nature of functional responses in natural settings and reveal how factors influencing functional responses can interact with one another through behavior and morphology. Further studies investigating the influence of multiple mechanisms on predator functional responses under field conditions will provide an increased understanding of the drivers of predator-prey interaction strengths and their consequences for communities and ecosystems. C_LI

ecology↗

Estimating predator functional responses using the times between prey captures

O_LIPredator functional responses, which describe how predator feeding rates change with prey densities, are a core component of predator-prey theory. Given their importance, ecologists have measured thousands of predator functional responses. However, most of these studies have used a single standard experimental method that is ill-suited to address many current, pressing questions regarding functional responses. C_LIO_LIWe derive a new experimental design and statistical analysis that quantifies the parameters of predator functional responses by using the time between a predators feeding events and can be used with individual predators requiring only one or a few trials. We examine the feasibility of this experimental method and analysis by using simulations to examine the ability of the statistical model to estimate the true functional response parameters from simulated data. We also perform a proof-of-concept experiment estimating the functional responses of two individual jumping spiders feeding on midges. C_LIO_LIOur simulations show that the statistical method is capable of reliably estimating functional response parameters under a wide range of parameter values and sample sizes. Our proof-of-concept experiment illustrates that the experimental design and statistical method provided reasonable estimates of functional response parameters and good fits to the data for individual jumping spiders using only a few trials per individual. C_LIO_LIBy virtue of the fewer number of trials required to measure a functional response, the method derived here promises to expand the questions that can be addressed using functional response experiments and the systems for which functional responses can be measured. For example, this method is well-poised to address questions such as intraspecific variation in predator functional response parameters and the role of predator and prey traits and abiotic conditions on shaping functional responses. We hope, therefore, that this time-between-captures method will refine our understanding of functional responses and thereby our understanding of predator-prey interactions more generally. C_LI

ecology↗

Nonlinear functional responses and ecological pleiotropy alter the strength of disruptive selection in consumers

Much of the theory on disruptive selection has focused on selection in generalist consumers caused by ecological opportunity through the availability of alternative resources and intraspecific competition for those resources. This theory, however, makes several ecologically unrealistic assumptions. First, this theory assumes that consumers have a linear, resource-dependent functional response, ignoring well-documented effects of resource handling times and consumer dependence. Second, this theory assumes that the trait under selection only influences the percapita attack rates of the consumer, ignoring other effects of the trait that may influence feeding rates and hence fitness. Here, I develop a one consumer-two resource model to investigate how nonlinear functional responses and ecological pleiotropy (traits that have multiple simultaneous ecological effects) influence the strength of disruptive selection. I find that handling times and interference among consumers are capable of altering disruptive selection by changing feeding rates differentially across consumer phenotypes. In particular, handling times cause a decrease in the strength of disruptive selection while the effects of interference depend on the mechanism through which interference occurs. The effects of handling times and interference, however, are dependent on whether and how ecological pleiotropy causes correlations between handling times or interference rates and attack rates. Overall, my results suggest that features defining the functional responses of consumers and the relationships among those features determine the likelihood and strength of disruptive selection. In particular, disruptive selection should be strongest in generalist populations composed of individual diet specialists who experience lower handling times and interference rates on the resources for which their attack rates are highest.

evolutionary biology↗

Quantifying predator dependence in the functional response of generalist predators.

A longstanding debate concerns whether functional responses are best described by prey-dependent versus ratio-dependent models. Theory suggests that ratio dependence can explain many food web patterns left unexplained by simple prey-dependent models. However, for logistical reasons, ratio dependence and predator dependence more generally have seen infrequent empirical evaluation and then only so in specialist predators, which are rare in nature. Here we develop an approach to simultaneously estimate the prey-specific attack rates and predator-specific interference rates of predators interacting with arbitrary numbers of prey and predator species. We apply the approach to field surveys and two field experiments involving two intertidal whelks and their full suite of potential prey. Our study provides strong evidence for the presence of weak predator dependence that is closer to being prey dependent than ratio dependent over manipulated and natural ranges of species abundances. It also indicates how, for generalist predators, even the qualitative nature of predator dependence can be prey-specific.\n\nAuthor contributionsCW contributed to method development, KC and IS performed the caging experiment, and MN conceived of the study, carried out the fieldwork and analyses, and wrote the manuscript.

ecology↗