Search USGSSearch

Geology topics

Steve T. Buckland

Publications and source records attributed to Steve T. Buckland.

4 recordsLinked to original sources

Improved abundance trajectories with Bayesian population dynamics model: Case study with a Hawaiian honeycreeper

Many wildlife monitoring programmes collect annual data on population abundance. The resulting abundance estimates fluctuate over time partly because of true population change and partly because of observation error. These two components of variation can be separated by fitting the estimates to a population dynamics model within a Bayesian state-space modelling framework. By constraining the population trajectory to be biologically realistic, more precise estimates can be obtained. Independent biological knowledge can be incorporated through choice of model structure and by specifying informative prior distributions on demographic parameters. We illustrate the approach using a 31-year point transect study of the Hawai’i ’ākepa ( Loxops coccineus ). We fitted five models, each making different assumptions about how population change, recruitment and/or adult survival varied over time. Overall, the ’ākepa geometric mean growth rate was 1.02, indicating an increasing population over the 31-year time series, although there were periods of slow decline potentially associated with low recruitment and more rapid recovery associated with pulses of high recruitment. Abundance estimates derived from the population models were substantially more precise than the ‘raw’ point transect estimates: 95% credible interval (CrI) was on average 51.7% (s.d. = 14.1%) narrower.

Hawaii

Accounting for spatial habitat and management boundaries when estimating forest bird population distribution and density: Inferences from a soap film smoother

Birds are often obligate to specific habitats which can result in study areas with complex boundaries due to sudden changes in vegetation or other features. This can result in study areas with concave arcs or that include holes of unsuitable habitat such as lakes or agricultural fields. Spatial models used to produce species’ distribution and density estimates need to respect such boundaries to make informed decisions for species conservation and management. The soap film smoother is one model for complex study regions which controls the boundary behaviour, ensuring realistic values at the edges of the region. We apply the soap film smoother to account for boundary effects and compare it with thin plate regression spline (TPRS) smooth and design-based conventional distance sampling methods to produce abundance estimates from point-transect distance sampling collected data on Hawai‘i ‘Ākepa Loxops coccineus in the Hakalau Forest Unit of the Big Island National Wildlife Refuge Complex, Hawai‘i Island, USA. The soap film smoother predicted zero or near zero densities in the northern part of the domain and two hotspots (in the southern and central parts of the domain). Along the boundary the soap film model predicted relatively high densities where ‘Ākepa occur in the adjacent forest and near zero elsewhere. The design-based and soap film abundance estimates were nearly identical. The width of the soap film confidence interval was 16.5% and 0.8% wider than the width of the TPRS smooth and design-based confidence intervals, respectively. The peaks in predicted densities along the boundary indicates leakage by the TPRS smooth. We provide a discussion of the statistical methods, biological findings and management implications of applying soap film smoothers to estimate forest bird population status.

Hawaii

Using density surface models to estimate spatio-temporal changes in population densities and trend

Precise measures of population abundance and trend are needed for species conservation; these are most difficult to obtain for rare and rapidly changing populations. We compare uncertainty in densities estimated from spatio–temporal models with that from standard design‐based methods. Spatio–temporal models allow us to target priority areas where, and at times when, a population may most benefit. Generalised additive models were fitted to a 31‐year time series of point‐transect surveys of an endangered Hawaiian forest bird, the Hawai‘i ‘ākepa Loxops coccineus . This allowed us to estimate bird densities over space and time. We used two methods to quantify uncertainty in density estimates from the spatio–temporal model: the delta method (which assumes independence between detection and distribution parameters) and a variance propagation method. With the delta method we observed a 52% decrease in the width of the design‐based 95% confidence interval (CI), while we observed a 37% decrease in CI width when propagating the variance. We mapped bird densities as they changed across space and time, allowing managers to evaluate management actions. Integrating detection function modelling with spatio–temporal modelling exploits survey data more efficiently by producing finer‐grained abundance estimates than are possible with design‐based methods as well as producing more precise abundance estimates. Model‐based approaches require switching from making assumptions about the survey design to assumptions about bird distribution. Such a switch warrants consideration. In this case the model‐based approach benefits conservation planning through improved management efficiency and reduced costs by taking into account both spatial shifts and temporal changes in population abundance and distribution.

Hawaii

Model-based approaches to deal with detectability: a comment on Hutto (2016)

In a recent paper, Hutto (2016a) challenges the need to account for detectability when interpreting data from point counts. A number of issues with model-based approaches to deal with detectability are presented, and an alternative suggested: surveying an area around each point over which detectability is assumed certain. The article contains a number of false claims and errors of logic, and we address these here. We provide suggestions about appropriate uses of distance sampling and occupancy modeling, arising from an intersection of design- and model-based inference.

Ecological Applications