Geology topics

Jamie N. Womble

Publications and source records attributed to Jamie N. Womble.

12 recordsLinked to original sources

USGS2024

The dynamics of sea otter prey selection under population growth and expansion

Sea otters ( Enhydra lutris ) were extirpated from much of their range in the North Pacific by the early 1900s but have made a remarkable recovery in Southeast Alaska. Sea otter populations have been particularly successful in Glacier Bay, Alaska, a protected tidewater glacier fjord with a diverse and productive nearshore habitat. Collection of sea otter foraging observations in Glacier Bay began in 1993, along with high-resolution aerial surveys that provide estimates of sea otter abundance and distribution. We integrated these two data sources to investigate how sea otter diet changed in space and time as sea otters established and spread across Glacier Bay. Specifically, we developed a multilevel Bayesian model to capture how sea otter diet at a location (the number, type, and size of prey collected) changed as a function of local cumulative otter abundance and the year in which the location was first occupied. This framework enabled us to estimate the sequence of sea otter prey selection and switching as prey populations responded to sea otter foraging pressure. We found that local sea otter diet changed substantially as the population established, shifting away from large urchins, crabs, and clams to Modiolus mussels and small urchins, and lastly to small clams and Mytilus mussels. We also found that sea otter diet at newly occupied sites changed as otters spread over the main channel and into the arms of Glacier Bay. Further, by 2019, sea otters across the bay were primarily foraging on small prey, regardless of the local occupancy history. The absence of a spatial gradient in the size of prey captured late in the study suggests that feedbacks between the top-down effects of sea otter foraging, sea otter dispersal processes, and local variation in habitat productivity may have homogenized the size structure of available prey across Glacier Bay.

Alaska↗

USGS2024

Understanding sea otter population change in southeast Alaska

Introduction The Southeast Alaska (SE) stock of northern sea otters ( Enhydra lutris kenyoni ) ranges from Cape Yakataga on the north to the Dixon Entrance on the south. During the maritime fur trade, sea otters were commercially harvested to near extinction in SE for their pelts and were presumed unlikely to naturally repopulate the region.

Alaska↗

USGS2023

Informing management of recovering predators and their prey with ecological diffusion models

The reintroduction and recovery of predators can be ecologically beneficial as well as socially and economically controversial. However, the growth and expansion of predator populations, and thus their ecological, social, and economic impacts, are not static but rather they vary in space and time. We propose a spatiotemporal statistical modeling framework based on ecological diffusion to better inform the ecology and management of recovering predators and their prey. We demonstrate its utility by applying it to a recovering sea otter ( Enhydra lutris ) population in Southeast Alaska, where sea otters were reintroduced in the late 1960s and have exhibited unprecedented population growth. Estimated parameters yield inferences about movement and population ecology, and our approach provides useful derived quantities, such as local abundance and carrying capacity as well as a quantity we term the equilibrium differential. We used our model to examine how density dependence and carrying capacity of sea otters vary spatially across a region. The diffusion modeling approach we present can be generalized for use in other instances of (re)colonization across taxa to inform management and conservation efforts.

Alaska↗

USGS2023

Revealing the extent of sea otter impacts on bivalve prey through multi-trophic monitoring and mechanistic models

Sea otters are apex predators that can exert considerable influence over the nearshore communities they occupy. Since facing near extinction in the early 1900s, sea otters are making a remarkable recovery in Southeast Alaska, particularly in Glacier Bay, the largest protected tidewater glacier fjord in the world. The expansion of sea otters across Glacier Bay offers both a challenge to monitoring and stewardship and an unprecedented opportunity to study the top-down effect of a novel apex predator across a diverse and productive ecosystem. Our goal was to integrate monitoring data across trophic levels, space, and time to quantify and map the predator–prey interaction between sea otters and butter clams Saxidomus gigantea , one of the dominant large bivalves in Glacier Bay and a favoured prey of sea otters. We developed a spatially-referenced mechanistic differential equation model of butter clam dynamics that combined both environmental drivers of local population growth and estimates of otter abundance from aerial survey data. We embedded this model in a Bayesian statistical framework and fit it to clam survey data from 43 intertidal and subtidal sites across Glacier Bay. Prior to substantial sea otter expansion, we found that butter clam density was structured by an environmental gradient driven by distance from glacier (represented by latitude) and a quadratic effect of current speed. Estimates of sea otter attack rate revealed spatial heterogeneity in sea otter impacts and a negative relationship with local shoreline complexity. Sea otter exploitation of productive butter clam habitat substantially reduced the abundance and altered the distribution of butter clams across Glacier Bay, with potential cascading consequences for nearshore community structure and function. Spatial variation in estimated sea otter predation processes further suggests that community context and local environmental conditions mediate the top-down influence of sea otters on a given prey. Overall, our framework provides high-resolution insights about the interaction among components of this food web and could be applied to a variety of other systems involving invasive species, epidemiology or migration.

Journal of Animal Ecology↗

USGS2023

Northern Sea Otter (Enhydra lutris kenyoni) population abundance and distribution across the southeast Alaska stock, summer 2022

In the summer of 2022, the U.S. Fish & Wildlife Service and partners successfully completed the first single-year, aerial photo survey of sea otters across the entire Southeast stock of northern sea otters. This document presents the latest findings from the 2022 Southeast Alaska Sea Otter Survey, providing up-to-date information regarding occupancy, abundance and carrying capacity. We collected two independent data streams of sea otter observations during the survey using novel image sensor technologies for marine wildlife surveys and recently developed statistical methods. We calculated an abundance estimate of 22,359 (95% Bayesian credible interval: 19,595, 25,290, CV = 0.064) sea otters. Based on the these results, the population size of the Southeast stock of northern sea otters is still increasing and below the estimated carrying capacity for the region of 48,083 (95% Bayesian credible interval: 40,575, 58,570) sea otters. Results from this report include the first updated abundance estimates for the Southeast stock of sea otters in 10 years, which will help inform stakeholders from across the region and addresses the top priority identified by the 2019 Southeast Sea Otter Stakeholder Working Group.

Alaska↗

USGS2021

Recursive Bayesian computation facilitates adaptive optimal design in ecological studies

Optimal design procedures provide a framework to leverage the learning generated by ecological models to flexibly and efficiently deploy future monitoring efforts. At the same time, Bayesian hierarchical models have become widespread in ecology and offer a rich set of tools for ecological learning and inference. However, coupling these methods with an optimal design framework can become computationally intractable. Recursive Bayesian computation offers a way to substantially reduce this computational burden, making optimal design accessible for modern Bayesian ecological models. We demonstrate the application of so-called prior-proposal recursive Bayes to optimal design using a simulated data binary regression and the real-world example of monitoring and modeling sea otters in Glacier Bay, Alaska. These examples highlight the computational gains offered by recursive Bayesian methods and the tighter fusion of monitoring and science that those computational gains enable.

Ecology↗

USGS2021

Diffusion modeling reveals effects of multiple release sites and human activity on a recolonizing apex predator

Background Reintroducing predators is a promising conservation tool to help remedy human-caused ecosystem changes. However, the growth and spread of a reintroduced population is a spatiotemporal process that is driven by a suite of factors, such as habitat change, human activity, and prey availability. Sea otters ( Enhydra lutris ) are apex predators of nearshore marine ecosystems that had declined nearly to extinction across much of their range by the early 20th century. In Southeast Alaska, which is comprised of a diverse matrix of nearshore habitat and managed areas, reintroduction of 413 individuals in the late 1960s initiated the growth and spread of a population that now exceeds 25,000. Methods Periodic aerial surveys in the region provide a time series of spatially-explicit data to investigate factors influencing this successful and ongoing recovery. We integrated an ecological diffusion model that accounted for spatially-variable motility and density-dependent population growth, as well as multiple population epicenters, into a Bayesian hierarchical framework to help understand the factors influencing the success of this recovery. Results Our results indicated that sea otters exhibited higher residence time as well as greater equilibrium abundance in Glacier Bay, a protected area, and in areas where there is limited or no commercial fishing. Asymptotic spread rates suggested sea otters colonized Southeast Alaska at rates of 1–8 km/yr with lower rates occurring in areas correlated with higher residence time, which primarily included areas near shore and closed to commercial fishing. Further, we found that the intrinsic growth rate of sea otters may be higher than previous estimates suggested. Conclusions This study shows how predator recolonization can occur from multiple population epicenters. Additionally, our results suggest spatial heterogeneity in the physical environment as well as human activity and management can influence recolonization processes, both in terms of movement (or motility) and density dependence.

Alaska↗

USGS2020

Modelling pinniped abundance and distribution by combining counts at terrestrial sites and in-water sightings

Pinnipeds are commonly monitored using aerial photographic surveys at land- or ice-based sites, where animals come ashore for resting, pupping, molting, and to avoid predators. Although these counts form the basis for monitoring population change over time, they do not provide information regarding where animals occur in the water, which is often of management and conservation interest. In this study, we developed a hierarchical model that links counts of pinnipeds at terrestrial sites to sightings-at-sea and estimates abundance, spatial distribution, and the proportion of time spent on land (attendance probability). The structure of the model also allows for the inclusion of predictors that may explain variation in ecological and observation processes. We applied the model to Steller sea lions ( Eumetopias jubatus ) in Glacier Bay, Alaska using counts of sea lions from aerial photographic surveys and opportunistic in-water sightings from vessel surveys. Glacier Bay provided an ideal test and application of the model because data are available on attendance probability based on long-term monitoring. We found that occurrence in the water was positively related to proximity to terrestrial sites, as would be expected for a species that engages in central-place foraging. The proportion of sea lions in attendance at terrestrial sites and overall abundance estimates were consistent with reports from the literature and monitoring programs. The model we describe has benefit and utility for park managers who wish to better understand the overlap between pinnipeds and visitors, and the framework that we present has potential for application across a variety of study systems and taxa.

Alaska↗

USGS2019

Nonlinear reaction–diffusion process models improve inference for population dynamics

Partial differential equations (PDEs) are a useful tool for modeling spatiotemporal dynamics of ecological processes. However, as an ecological process evolves, we need statistical models that can adapt to changing dynamics as new data are collected. We developed a model that combines an ecological diffusion equation and logistic growth to characterize colonization processes of a population that establishes long-term equilibrium over a heterogeneous environment. We also developed a homogenization strategy to statistically upscale the PDE for faster computation and adopted a hierarchical framework to accommodate multiple data sources collected at different spatial scales. We highlighted the advantages of using a logistic reaction component instead of a Malthusian component when population growth demonstrates asymptotic behavior. As a case study, we demonstrated that our model improves spatiotemporal abundance forecasts of sea otters in Glacier Bay, Alaska. Furthermore, we predicted spatially varying local equilibrium abundances as a result of environmentally driven diffusion and density-regulated growth. Integrating equilibrium abundances over the study area in our application enabled us to infer the overall carrying capacity of sea otters in Glacier Bay, Alaska.

Alaska↗

USGS2018

Monitoring dynamic spatio-temporal ecological processes optimally

Population dynamics vary in space and time. Survey designs that ignore these dynamics may be inefficient and fail to capture essential spatio‐temporal variability of a process. Alternatively, dynamic survey designs explicitly incorporate knowledge of ecological processes, the associated uncertainty in those processes, and can be optimized with respect to monitoring objectives. We describe a cohesive framework for monitoring a spreading population that explicitly links animal movement models with survey design and monitoring objectives. We apply the framework to develop an optimal survey design for sea otters in Glacier Bay. Sea otters were first detected in Glacier Bay in 1988 and have since increased in both abundance and distribution; abundance estimates increased from 5 otters to >5,000 otters, and they have spread faster than 2.7 km/yr. By explicitly linking animal movement models and survey design, we are able to reduce uncertainty associated with forecasting occupancy, abundance, and distribution compared to other potential random designs. The framework we describe is general, and we outline steps to applying it to novel systems and taxa.

Ecology↗

USGS2017

Estimating occupancy and abundance using aerial images with imperfect detection

Species distribution and abundance are critical population characteristics for efficient management, conservation, and ecological insight. Point process models are a powerful tool for modelling distribution and abundance, and can incorporate many data types, including count data, presence-absence data, and presence-only data. Aerial photographic images are a natural tool for collecting data to fit point process models, but aerial images do not always capture all animals that are present at a site. Methods for estimating detection probability for aerial surveys usually include collecting auxiliary data to estimate the proportion of time animals are available to be detected. We developed an approach for fitting point process models using an N -mixture model framework to estimate detection probability for aerial occupancy and abundance surveys. Our method uses multiple aerial images taken of animals at the same spatial location to provide temporal replication of sample sites. The intersection of the images provide multiple counts of individuals at different times. We examined this approach using both simulated and real data of sea otters ( Enhydra lutris kenyoni ) in Glacier Bay National Park, southeastern Alaska. Using our proposed methods, we estimated detection probability of sea otters to be 0.76, the same as visual aerial surveys that have been used in the past. Further, simulations demonstrated that our approach is a promising tool for estimating occupancy, abundance, and detection probability from aerial photographic surveys. Our methods can be readily extended to data collected using unmanned aerial vehicles, as technology and regulations permit. The generality of our methods for other aerial surveys depends on how well surveys can be designed to meet the assumptions of N -mixture models.

Methods in Ecology and Evolution↗

USGS2017

An integrated data model to estimate spatiotemporal occupancy, abundance, and colonization dynamics

Ecological invasions and colonizations occur dynamically through space and time. Estimating the distribution and abundance of colonizing species is critical for efficient management or conservation. We describe a statistical framework for simultaneously estimating spatiotemporal occupancy and abundance dynamics of a colonizing species. Our method accounts for several issues that are common when modeling spatiotemporal ecological data including multiple levels of detection probability, multiple data sources, and computational limitations that occur when making fine-scale inference over a large spatiotemporal domain. We apply the model to estimate the colonization dynamics of sea otters ( Enhydra lutris ) in Glacier Bay, in southeastern Alaska.

Ecology↗