Geology ReportsSearch

Geology topics

Brian W. Rolek

Publications and source records attributed to Brian W. Rolek.

11 recordsLinked to original sources

American kestrel population trends and vital rates at the continental scale

The American kestrel ( Falco sparverius , hereafter referred to as kestrel) has declined across much of its North American range since at least the mid-1960s. Kestrel population dynamics have been explored through a multitude of local studies and two broad reviews of available data. Across large geographic extents, however, the demographic cause(s) of kestrel population declines remain(s) largely unknown. As part of a collaborative effort to elucidate the drivers of kestrel population declines, we developed a continental-scale integrated population model using band-recovery data, productivity data, and Breeding Bird Survey indices from 1986 to 2019 to estimate indices of annual population sizes, survival, and productivity rates across the continental United States. We detected a decline in population size of ~1%–2% per year. Overall estimates of population growth from 1986 to 2019 suggest a 29% decline in population size (95% CI = −34% to −23%). There was little evidence of a trend in brood size. However, survival of juvenile birds (mean = −0.015, SD = 0.008 and mean = −0.024, SD = 0.010 for females and males, respectively) and adult males (mean = −0.016, SD = 0.010) in the summer declined, suggesting that these vital rates could be contributing to declines in populations over time. Winter adult survival rates (mean = −0.004, SD = 0.009 and mean = −0.009, SD = 0.010 for females and males, respectively) also declined but to a lesser extent than summer survival. For juvenile birds, winter survival increased (mean = 0.006, SD = 0.008 and mean = 0.002, SD = 0.009 for females and males, respectively); however, this was not enough to offset declines in summer survival and annual survival rates declined over the time series. Annual adult survival was also low relative to previous research on kestrel survival rates. Given the importance of survival to population trends, our findings provide support for several previously proposed broad classes of factors potentially contributing to observed population declines: declines in arthropod prey, second-generation rodenticides, neonicotinoid insecticides, and predation.

Ecosphere

Reanalysis ignores pertinent data, includes inappropriate observations, and disregards realities of applied ecology: Response to Huso and Dalthorp (2023)

1) We recently demonstrated efficacy of automated curtailment of wind turbines in reducing fatalities of eagles at a study site in Wyoming, USA. Huso and Dalthorp criticize our work, asserting that there are several ‘major errors’ that render our previous work as providing ‘no meaningful support’ for automated curtailment. As we show here, our data do indeed provide support for the efficacy of automated curtailment. 2) The purported major errors they identify include: having only 1 year of post-treatment data, having only one control and one treatment site, using the control site for inference, choosing an arbitrary demarcation date between the ‘before’ and ‘after’ periods, analysing the number, rather than the rate, of fatalities, and not including data they consider pertinent. These claims are unsupported because all result from misreading our study, ignoring realities of causal inference in field ecology, or are matters of preference. 3) Most importantly, we did not fail to include pertinent data and we provided sufficient criteria in the manuscript to explain inclusion of carcasses in our study. As stated in our previous study, the eagle carcasses we did not include were found either outside of search areas or incidentally, and thus did not meet criteria for inclusion. Further, Huso and Dalthorp present a standard for spatial and temporal replication that is inconsistent with their own recent work and many other studies in this field. Finally, their reanalysis of our data ignores the control site while including inappropriate data and thus is not suitable for inference. 4) We appreciate the unusually thorough critique of our work provided by Huso and Dalthorp. Despite the major errors in their argument, this discussion provides a platform for further evaluation of our original work. 5) Synthesis and applications . We show that incorporating control site data and using our a priori demarcation of before and after periods into Huso and Dalthorp's reanalysis returns meaningful support for automated curtailment. We also direct the reader to an updated analysis that uses components of the approach Huso and Dalthorp suggest, along with additional data and a number of other analytical improvements, to validate and strengthen our original conclusions.

Journal of Applied Ecology

Variation in flight characteristics associated with entry by eagles into rotor-swept zones of wind turbines

Automated curtailment of wind turbines can reduce fatality rates of wildlife, but the resulting increased number of curtailments can reduce power generation. Tailoring curtailment criteria for each individual turbine could reduce unnecessary curtailment, yet it is unknown whether the risk to wildlife varies among turbines. We demonstrate turbine-specific variation in the speed, altitude, approach angle, and distance metrics associated with entry by eagles into rotor-swept zones. Our results thus illustrate the potential value of turbine-specific curtailment criteria to reduce fatality rates of wildlife at wind energy facilities.

Ibis

Confirmation that eagle fatalities can be reduced by automated curtailment of wind turbines

Automated curtailment is potentially a powerful technique to reduce collision mortality of wildlife with wind turbines. Previously, we used a before–after–control–impact framework to demonstrate that eagle fatalities declined after automated curtailment was implemented with the IdentiFlight system at a wind power facility in Wyoming, USA. We received substantial interest and feedback regarding our study and, here, we implement several analytical suggestions and include more recent data that strengthen the inference we draw from our results. The five main analytical suggestions we received were to (1) exclude from analysis data that were collected during the period when automated curtailment was only partially implemented; (2) only analyse data from a single make and model of turbine; (3) evaluate changes in the rate of fatality, instead of the yearly numbers of fatalities that result from fluctuations around that rate; (4) calculate a standard measure determining effects of a treatment in a before–after–control–impact study and (5) examine yearly fluctuations of the fatality rate during the before period. After incorporating these suggestions and including additional data collected since the prior paper was published, our results confirm prior work. We demonstrate that eagle fatalities were reduced by 85% (95% highest density interval = 12%, 100%) after implementation of automated curtailment. Rate of fatalities declined by 2.85 eagles per year (−0.67, 5.70) between before and after periods at the treatment site and increased by 2.26 eagles per year (−1.77, 7.37) at the control site. Overall, the fatality rate declined by 4.91 (−0.27, 11.27) more eagles per year at the treatment site than at the control site. The probability that the fatality rate declined at the treatment site relative to the control site was 0.97. Our re-analysis strengthens our inference by using more robust analyses and data to support the conclusions of the prior study suggesting that automated curtailment was effective at reducing eagle fatalities at our treatment site. Because of the site- and species-specific nature of our work, future research should examine the efficacy of automated curtailment at other sites, with other species, and under different curtailment regimes.

Ecological Solutions and Evidence

Flight characteristics forecast entry by eagles into rotor-swept zones of wind turbines

Operators of wind power facilities can mitigate wildlife mortality by slowing or stopping wind turbines (hereafter ‘curtail’) when birds are at an increased risk of collision. Some facility operators curtail when individual birds have flight characteristics (e.g. altitude, distance or relative bearing of a bird's flight path) that exceed some threshold value, but thresholds currently in use have not been empirically evaluated. Overly restrictive thresholds can cause turbine curtailment for birds that never enter rotor-swept zones, thereby resulting in excess power loss. We evaluated the probability that birds, specifically eagles, entered the rotor-swept zone (hereafter ‘entry probability’) in response to their flight characteristics. We used an automated monitoring system to classify individuals as eagles or non-eagles and record flight paths of purported eagles at a wind facility in Wyoming, USA. We used logistic regression with occupancy dynamics and a distance-dependent colonization process to model entry probability. As a result, this model allowed entry probability to decrease with horizontal distance to the nearest turbine. The probability of entry varied with distance to the nearest turbine and approached zero when that distance was more than 202 m. Entry probability peaked when eagles flew 89 m above ground, corresponding to hub heights of turbines (80 m), and decreased to near-zero at altitudes of 189 m or more. Entry probabilities were greatest when flight paths were near the rotor-swept zone and when eagles flew slowly toward the nearest turbine. Compass bearing of a flight path was not associated with entry probability. Our model accurately forecasted entry probability in Wyoming (area under the curve (AUC) = 0.96) and was transferable to another facility in California, USA (AUC = 0.97); therefore, our results may be applicable across a variety of settings. Curtailment criteria can be based on flight path characteristics to forecast entry into rotor-swept zones. The use of distance and altitude thresholds when making curtailment decisions is justified. However, this analysis suggests alteration of the time to collision threshold, with curtailment initiated at greater distances as the speed of the bird decreases. Our novel modelling method and our results can inform curtailment criteria in any situation where curtailment decisions are made in real-time.

Wyoming

Flight altitudes of raptors in southern Africa highlight vulnerability of threatened species to wind turbines

Energy infrastructure, particularly for wind power, is rapidly expanding in Africa, creating the potential for conflict with at-risk wildlife populations. Raptor populations are especially susceptible to negative impacts of fatalities from wind energy because individuals tend to be long-lived and reproduce slowly. A major determinant of risk of collision between flying birds and wind turbines is the altitude above ground at which a bird flies. We examine 18,710 observations of flying raptors recorded in southern Africa and we evaluate, for 49 species, the frequency with which they were observed to fly at the general height of a wind turbine rotor-swept zone (50–150 m). Threatened species, especially vultures, were more likely to be observed at turbine height than were other species, suggesting that these raptors are most likely to be affected by wind power development across southern Africa. Our results highlight that threatened raptor species, particularly vultures, might be especially impacted by expanded wind energy infrastructure across southern Africa.

Frontiers in Ecology and Evolution

Eagles enter rotor-swept zones of wind turbines at rates that vary per turbine

There is increasing pressure on wind energy facilities to manage or mitigate for wildlife collisions. However, little information exists regarding spatial and temporal variation in collision rates, meaning that mitigation is most often a blanket prescription. To address this knowledge gap, we evaluated variation among turbines and months in an aspect of collision risk—probability of entry by an eagle into a rotor-swept zone (hereafter, “probability of entry”). We examined 10,222 eagle flight paths identified and recorded by an automated bird monitoring system at a wind energy facility in Wyoming, USA. Probabilities of entry per turbine–month combination were 4.03 times greater in some months than others, ranging 0.15 to 0.62. The overall probability of entry for the riskiest turbine (i.e., the one with the greatest probability of entry) was 2.39 times greater than the least-risky turbine. Our methodology describes large variation across turbines and months in the probability of entry. If subsequently combined with information on other sources of variation (i.e., weather, topography), this approach can identify risky versus safe situations for eagles under which cost of management, curtailment prescriptions, and collision risk can be simultaneously minimized.

Wyoming

Habitat associations of breeding conifer-associated birds in managed and regenerating forested stands

Forests are often affected by management that could influence demographics of breeding and post-breeding birds that reside within. Numerous studies have focused on immediate effects from management on wildlife soon after forestry treatment (e.g., 0–5 years), however, fewer studies have examined changes in focal species abundance over longer durations as a forest regenerates after disturbance. We examined how forest management influenced 18 conifer-associated birds during breeding and post-breeding over the forest regeneration period in a landscape dominated by forestry. To achieve this, we paired avian detection data from point count surveys in lowland conifer and mixed-wood forests with Bayesian distance-removal models and an information-theoretic framework. We estimated abundance and associations with seven common forestry treatment categories applied at the stand scale, years-since-harvest (YSH; 5–120+), and seven vegetation variables measured within stands. Forestry treatment categories and YSH were poor predictors of abundance, and none of the 14 species with good-fitting models had associations with these covariates. Twelve of 13 species with good-fitting models had important associations between abundance and vegetation variables. All vegetation variables were associated with abundance of some species, irrespective of the forestry treatment in which the site occurred, including spruce-fir tree composition (seven species), tree basal area (six species), midstory cover (five species), live crown ratio (three species), shrub cover (three species), tree diameter at breast height (two species), and shrub composition (one species). In a companion study, several species assemblages were associated with vegetation variables (i.e., spruce-fir tree composition, tree basal area, and tree diameter at breast height) that varied with YSH and forestry treatments, suggesting that some forestry treatments may indirectly influence avian abundance when certain vegetation outcomes are achieved. Our results suggest that managers should target species-specific vegetation outcomes rather than more broadly categorized forestry treatment types when managing for individual focal species because of large variations in vegetative outcomes across stands within a forest treatment category. Our study informs management and conservation of biodiversity in regions such as the Atlantic Northern Forest where commercial forestry is the dominant human land use.

Maine, New Hampshire, Vermont

Yearly temperature fluctuations and survey speed influence road counts of wintering raptors

Globally, evaluation of population trends is the most pressing research need for many species of conservation concern. Road counts for birds of prey are useful for monitoring long‐term population trends and examining year‐to‐year variations in abundance. We examined data from 2155 road surveys conducted from 2001 to 2018 by community scientists who recorded > 85 000 individuals of 14 species of raptors while participating in the Pennsylvania Winter Raptor Survey, in Pennsylvania, USA. We estimated abundance and population growth rates while accounting for observation error by using dynamic Bayesian state‐space models. Model estimates indicated that counts of wintering Bald Eagles Haliaeetus leucocephalus, Red‐shouldered Hawks Buteo lineatus and Black Vulture Coragyps atratus increased over the course of the study. Counts of Rough‐legged Buzzard Buteo lagopus , Red‐tailed Hawk Buteo jamaicensis , Northern Harrier Circus hudsonius , Turkey Vulture Cathartes aura and American Kestrel Falco sparverius varied more (CV > 5.0) over the duration of the study than other species did. Higher winter temperatures were associated with increases in counts of species whose local populations are partially migratory (American Kestrel and Red‐tailed Hawk), and with lower counts of a long‐distance arctic migrant – Rough‐legged Buzzard. Counts of these species were therefore correlated such that more American Kestrels and Red‐tailed Hawks were counted during years when Rough‐legged Buzzards were less frequently seen. Generally, the number of individuals counted declined as survey speed increased. A general rule for road counts therefore seems to be ‘slower is better’, consistent with past recommendations that observers travel at a speed < 40 km/h during road counts. Our study highlights the utility of road surveys and advances analytical approaches to monitor raptors.

Ibis

Regenerating clearcuts combined with postharvest forestry treatments promote habitat for breeding and post-breeding spruce-fir avian assemblages in the Atlantic Northern Forest

The quantity of spruce-fir forest and some conifer-associated breeding bird abundances in the Atlantic Northern Forest have declined in recent decades emphasizing the need to better understand avian responses to forest management and to identify options that proactively conserve habitat for birds during the breeding and post-breeding period. We conducted avian point counts and vegetation surveys on publicly and privately-owned lands with known management histories to assess relationships between avian assemblages in harvest and postharvest treatments that could provide habitat for passerine birds associated with the spruce-fir forest type. We sampled regenerating conifer-dominated stands 5–41 years-since-harvest (YSH) in three harvest treatments (selection, irregular first-stage shelterwood, and clearcuts) and three postharvest treatments including regenerating clearcuts treated with aerially applied herbicide (e.g., glyphosate), precommercial thinning (PCT), both herbicide and PCT, and mature stands (≥48 YSH). Spruce-fir obligate and associate birds were more abundant in stands with greater spruce-fir tree composition (≥70% and ≥60%, respectively). Avian richness of spruce-fir obligates, associates, and species of concern was greater in clearcuts and clearcuts with postharvest treatments. Vegetative features associated with greater richness and abundance of spruce-fir birds, such as greater spruce-fir composition and smaller tree diameter at breast height, were prominent in regenerating clearcuts and postharvest treatments and suggested that these management practices promote local abundances and richness of spruce-fir birds. Richness and abundances of spruce-fir birds were least in selection, shelterwood, and mature stands, and vegetative features associated with greater richness and abundance of spruce-fir birds were diminished in these stands. Forestry trends in Maine indicate that the extent of the clearcut suite of treatments has decreased on the landscape while selection and shelterwood harvests have increased. Thus, changes in incentives for managers to apply even-aged management coupled with post-harvest applications of herbicides or precommercial thinning might mitigate further declines in habitat for spruce-fir passerines assemblages. A greater ratio of clearcuts with postharvest treatments 11–40 YSH compared to other treatments (mature forest ≥48 YSH, selection and shelterwood 5–41 YSH) would maintain diverse spruce-fir bird communities on the landscape. Use of clearcuts with postharvest treatments in the hemiboreal forests of northern New England, southern Quebec, and Maritime Provinces of eastern Canada may enhance habitat for breeding and post-breeding spruce-fir birds, especially where the quantity of conifer forests are declining and residual patches of conifers are increasingly fragmented.

Atlantic Northern Forest

Landscape capability models as a tool to predict fine-scale forest bird occupancy and abundance

Context Species-specific models of landscape capability (LC) can inform landscape conservation design. Landscape capability is “the ability of the landscape to provide the environment […] and the local resources […] needed for survival and reproduction […] in sufficient quantity, quality and accessibility to meet the life history requirements of individuals and local populations.” Landscape capability incorporates species’ life histories, ecologies, and distributions to model habitat for current and future landscapes and climates as a proactive strategy for conservation planning. Objectives We tested the ability of a set of LC models to explain variation in point occupancy and abundance for seven bird species representative of spruce-fir, mixed conifer-hardwood, and riparian and wooded wetland macrohabitats. Methods We compiled point count data sets used for biological inventory, species monitoring, and field studies across the northeastern United States to create an independent validation data set. Our validation explicitly accounted for underestimation in validation data using joint distance and time removal sampling. Results Blackpoll warbler ( Setophaga striata ), wood thrush ( Hylocichla mustelina ), and Louisiana ( Parkesia motacilla ) and northern waterthrush ( P. noveboracensis ) models were validated as predicting variation in abundance, although this varied from not biologically meaningful (1%) to strongly meaningful (59%). We verified all seven species models [including ovenbird ( Seiurus aurocapilla ), blackburnian ( Setophaga fusca ) and cerulean warbler ( Setophaga cerulea )], as all were positively related to occupancy data. Conclusions LC models represent a useful tool for conservation planning owing to their predictive ability over a regional extent. As improved remote-sensed data become available, LC layers are updated, which will improve predictions.

Landscape Ecology