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At least 595 records · Page 33Linked to original sources

Modelling non-Euclidean movement and landscape connectivity in highly structured ecological networks

Movement is influenced by landscape structure, configuration and geometry, but measuring distance as perceived by animals poses technical and logistical challenges. Instead, movement is typically measured using Euclidean distance, irrespective of location or landscape structure, or is based on arbitrary cost surfaces. A recently proposed extension of spatial capture-recapture (SCR) models resolves this issue using spatial encounter histories of individuals to calculate least-cost paths (ecological distance: Ecology , 94 , 2013, 287) thereby relaxing the Euclidean assumption. We evaluate the consequences of not accounting for movement heterogeneity when estimating abundance in highly structured landscapes, and demonstrate the value of this approach for estimating biologically realistic space-use patterns and landscape connectivity. We simulated SCR data in a riparian habitat network, using the ecological distance model under a range of scenarios where space-use in and around the landscape was increasingly associated with water (i.e. increasingly less Euclidean). To assess the influence of miscalculating distance on estimates of population size, we compared the results from the ecological and Euclidean distance based models. We then demonstrate that the ecological distance model can be used to estimate home range geometry when space use is not symmetrical. Finally, we provide a method for calculating landscape connectivity based on modelled species-landscape interactions generated from capture-recapture data. Using ecological distance always produced unbiased estimates of abundance. Explicitly modelling the strength of the species-landscape interaction provided a direct measure of landscape connectivity and better characterised true home range geometry. Abundance under the Euclidean distance model was increasingly (negatively) biased as space use was more strongly associated with water and, because home ranges are assumed to be symmetrical, produced poor characterisations of home range geometry and no information about landscape connectivity. The ecological distance SCR model uses spatially indexed capture-recapture data to estimate how activity patterns are influenced by landscape structure. As well as reducing bias in estimates of abundance, this approach provides biologically realistic representations of home range geometry, and direct information about species-landscape interactions. The incorporation of both structural (landscape) and functional (movement) components of connectivity provides a direct measure of species-specific landscape connectivity.

Methods in Ecology and Evolution↗

Hatchling emergence ecology of Ouachita map turtles (Graptemys ouachitensis) on the lower Wisconsin River, Wisconsin, USA

Despite its biological importance in shaping both individual fitness and population structure, much remains to be learned about the hatchling emergence ecology of most freshwater turtles. Here, we provide some of the first details on these early life stages for the Ouachita map turtle ( Graptemys ouachitensis ) obtained during 2015–2017 along the lower Wisconsin River, Iowa County, Wisconsin, and integrate our results into related research within the genus Graptemys . Dedicated trail cameras over in situ turtle nests provided otherwise difficult to obtain observational data relevant to natural hatchling emergence without disturbing nests or hatchlings. In contrast to some earlier reports for Graptemys , hatchling emergence was mostly diurnal and synchronous, primarily in the morning soon after soil temperatures began to rise from overnight low values. Data suggest a temperature change model of cueing hatchling emergence, which may represent a local or regional adaptation to reduce nocturnal predation risks, mostly from raccoons ( Procyon lotor ), or may simply reflect default diurnal hatchling activity patterns when not affected by thermal constraints. Aside from predation, hatchlings on this small study site are affected by vegetative shading, leading to relatively long times to first emergence periods (mean, 82.3 d), low mean nest temperatures (25.9°C), and a likely male-biased sex ratio. These findings highlight the value of hatchling emergence studies in revealing important influences on population viability and in guiding appropriate habitat management in conservation efforts.

Wisconsin↗

Estimating traffic volume and road age in Wyoming to inform resource management planning: An application with wildlife-vehicle collisions

Road networks and their associated vehicular traffic disturb many terrestrial systems, but inventories of roads used to assess these effects often focus on the ‘where’ (e.g., local road type and density) and neglect the ‘when’ (e.g., temporal disturbance) or ‘how much’ (e.g., traffic volume disturbance). We developed annual estimates of the ‘when’ (road age) and ‘how much’ (vehicular traffic volume) across 148,172 km of highways, arterials, collectors, local, and gravel/graded roads within the state of Wyoming for the years 1986 to 2020 to provide a comprehensive dataset for future ecological investigations. We leveraged a suite of ancillary data on surface disturbances (e.g., oil & gas drilling operations, wind turbines, and open pit mines) with known establishment dates and combined them using graph theory and centrality metrics to estimate the age of each road. We then predicted traffic volume obtained from the Wyoming Department of Transportation for each year across Wyoming using a machine learning method, XGBoost, and a separate set of spatial covariates hypothesized to explain traffic patterns across large regions. We found that 132,476 km of these roads likely existed before 1986, but that 16,693 km (10.7 %) of roads have been built since 1986. Overall, our estimates of road age were 89 % accurate when assessed on a subset of 1,330 roads with high-resolution aerial imagery. Mean absolute error for predicting traffic volume ranged from 35.2 to 77.9 annual average daily traffic (aadt) for trucks and 269.2 to 516.7 aadt for all-vehicles across the 35 years. We found that mean traffic volume across the state increased by 23 % for both truck-only traffic and all vehicular traffic from 1986 to 2020. However, changes in traffic volume have varied substantially across the state (e.g., 100 % increases in volume in some areas, while other areas experienced declines of up to 1,786 %). We also illustrate a novel application of these data by predicting rates of reported wildlife-vehicle collisions (WVCs) along a subset of roads. We found evidence of a non-linear relationship that supported a threshold hypothesis for WVCs, wherein increases in traffic volume equate to increases in WVCs up to a threshold, above which increases in traffic volume result in declines in WVCs. The data provided here will enable better-informed studies of road ecology to address how roads may affect wildlife populations and key ecosystems across Wyoming.

Wyoming↗

Co-mast: Harmonized seed production data for woody plants across US long-term research sites

Plants display a range of temporal patterns of inter-annual reproduction, from relatively constant seed production to “mast seeding,” the synchronized and highly variable interannual seed production of plants within a population. Previous efforts have compiled global records of seed production in long-lived plants to gain insight into seed production, forest and animal population dynamics, and the effects of global change on masting. Existing datasets focus on seed production dynamics at the population scale but are limited in their ability to examine community-level mast seeding dynamics across different plant species at the continental scale. We harmonized decades of plant reproduction data for 141 woody plant species across nine Long-Term Ecological Research (LTER) or long-term ecological monitoring sites from a wide range of habitats across the United States. Plant reproduction data are reported annually between 1957 and 2021 and based on either seed traps or seed and/or cone counts on individual trees. A wide range of woody plant species including trees, shrubs, and lianas are represented within sites allowing for direct community-level comparisons among species. We share code for filtering of data that enables the comparison of plot and individual tree data across sites. For each species, we compiled relevant life history attributes (e.g., seed mass, dispersal syndrome, seed longevity, sexual system) that may serve as important predictors of mast seeding in future analyses. To aid in phylogenetically informed analyses, we also share a phylogeny and phylogenetic distance matrix for all species in the dataset. These data can be used to investigate continent-scale ecological properties of seed production, including individual and population variability, synchrony within and across species, and how these properties of seed production vary in relation to plant species traits and environmental conditions. In addition, these data can be used to assess how annual variability in seed production is associated with climate conditions and how that varies across populations, species, and regions. The dataset is released under a CC0 1.0 Universal public domain license.

Ecology↗

Integrating growth and survival models for flexible estimation of size-dependent survival in a cryptic, endangered snake

Estimates of demographic rates for animal populations and individuals have many applications for ecological and conservation research. In many animals, survival is size-dependent, but estimating the form of the size–survival relationship presents challenges. For elusive species with low recapture rates, individuals’ size will be unknown at many points in time. Integrating growth and capture–mark–recapture models in a Bayesian framework empowers researchers to impute missing size data, with uncertainty, and include size as a covariate of survival, capture probability, and presence on-site. If there is no theoretical expectation for the shape of the size–survival relationship, spline functions can allow for fitting flexible, data-driven estimates. We use long-term capture–mark–recapture data from the endangered San Francisco gartersnake ( Thamnophis sirtalis tetrataenia ) to fit an integrated growth–survival model. Growth models showed that females reach longer asymptotic lengths than males and that the magnitude of sexual size dimorphism differed among populations. The capture probability and availability of San Francisco gartersnakes for capture increased with snout–vent length. The survival rate of female snakes exhibits a nonlinear relationship with snout–vent length (SVL), with survival flat between 300 mm and 550 mm SVL before decreasing for females between 550 mm and 700 mm SVL. For male snakes, survival decreased for adult males >550 mm SVL. The survival rates of the smallest and largest San Francisco gartersnakes were highly uncertain because recapture rates were very low for these sizes. By integrating growth and survival models and using penalized splines, we found support for size-dependent survival in San Francisco gartersnakes. Our results have applications for devising management activities for this endangered subspecies, and our methods could be applied broadly to the study of size-dependent demography among animals.

California↗

Estimation of density and population size and recommendations for monitoring trends of Bahama parrots on Great Abaco and Great Inagua

Once abundant and widely distributed, the Bahama parrot (Amazona leucocephala bahamensis) currently inhabits only the Great Abaco and Great lnagua Islands of the Bahamas. In January 2003 and May 2002-2004, we conducted point-transect surveys (a type of distance sampling) to estimate density and population size and make recommendations for monitoring trends. Density ranged from 0.061 (SE = 0.013) to 0.085 (SE = 0.018) parrots/ha and population size ranged from 1,600 (SE = 354) to 2,386 (SE = 508) parrots when extrapolated to the 26,154 ha and 28,162 ha covered by surveys on Abaco in May 2002 and 2003, respectively. Density was 0.183 (SE = 0.049) and 0.153 (SE = 0.042) parrots/ha and population size was 5,344 (SE = 1,431) and 4,450 (SE = 1,435) parrots when extrapolated to the 29,174 ha covered by surveys on Inagua in May 2003 and 2004, respectively. Because parrot distribution was clumped, we would need to survey 213-882 points on Abaco and 258-1,659 points on Inagua to obtain a CV of 10-20% for estimated density. Cluster size and its variability and clumping increased in wintertime, making surveys imprecise and cost-ineffective. Surveys were reasonably precise and cost-effective in springtime, and we recommend conducting them when parrots are pairing and selecting nesting sites. Survey data should be collected yearly as part of an integrated monitoring strategy to estimate density and other key demographic parameters and improve our understanding of the ecological dynamics of these geographically isolated parrot populations at risk of extinction.

Wildlife Society Bulletin↗

Evaluating the status of individuals and populations: Advantages of multiple approaches and time scales

The assessment of population status is a central goal of applied wildlife research and essential to the field of wildlife conservation. “Population status” has a number of definitions, the most widely used having to do with the current trajectory of the population (i.e., growing, stable, or declining), or the probability of persistence (i.e., extinction risk), perhaps without any specific knowledge as to the factors driving a population’s dynamics. In contrast, a population’s status relative to the carrying capacity of the environment ( K ) is an ecologically-based definition that explicitly provides information about a major mechanism of population control. That is, it relates to the relative per capita availability of resources to individuals in a population, which can also be used to infer the state of the environment itself. Sea otters in the North Pacific provide an excellent system with which to examine various approaches to assessing population status relative to K . This is because sea otters were nearly extirpated by historic commercial overexploitation in the eighteenth and nineteenth centuries, followed by natural and translocation-aided population recovery during the twentieth century, and this decline and recovery has been relatively well documented. This provided a unique opportunity to study populations at the extremes of the population status spectrum. Here we describe and review the approaches that have been utilized in sea otter research to understand the status of populations relative to resource abundance. Specifically, we will illustrate the utility of various indices of population status for understanding population dynamics using the case study of a second precipitous sea otter decline in the Western Aleutians. The indices or “tools” described here fit into several broad categories including (1) energetic, (2) morphological, and (3) demographic as well as a fourth category of emerging tools that have not yet been employed in many other situations including dietary diversity, community structure, spatial distribution, and gene expression. Overall, a variety of indices used to measure population status throughout the sea otter’s range have provided insights for understanding the mechanisms driving the trajectory of various sea otter populations, which a single index could not, and we suggest using multiple methods to measure a population’s status at multiple spatial and temporal scales. The work described here also illustrates the usefulness of long-term data sets and/or approaches that can be used to assess population status retrospectively, providing information otherwise not available. While not all systems will be as amenable to using all the approaches presented here, we expect innovative researchers could adapt analogous multi-scale methods to a broad range of habitats and species including apex predators occupying the top trophic levels, which are often of conservation concern.

Book chapter↗

Robustness of closed capture-recapture methods to violations of the closure assumption

Closed-population capture–recapture methods have been used extensively in animal ecology, both by themselves and within the context of Pollock’s robust design and multistate models, to estimate various parameters of population and community dynamics. The defining assumption of geographic and demographic closure (i.e., no births, deaths, immigration, or emigration) for the duration of sampling is restrictive and is likely to be violated in many field situations. I evaluated several types of violations of the closure assumption and found that completely random movement in and out of a study area does not introduce bias to estimators from closed-population methods, although it decreases precision. In addition, if capture probabilities vary only with time, the closed-population Lincoln-Petersen estimator is unbiased for the size of the superpopulation when there are only births/immigration or only deaths/emigration. However, for other cases of nonrandom movement, closed-population estimators were biased when movement was Markovian (dependent on the presence/absence of the animal in the previous time period), when an animal was allowed one entry to and one exit from the study area, or when there was trap response or heterogeneity among animals in capture probability. In addition, the probability that an animal is present and available for capture (e.g., breeding propensity) can be estimated using Pollock’s robust design only when movement occurs at a broader temporal scale than that of sampling.

Ecology↗

Comparative demography of new world populations of thrushes (Turdus spp.): Comment

Survival and fecundity are fundamental to the study of evolutionary ecology, as they are two of the key variables influencing the constrained optimization process we call natural selection. Likewise, population managers require accurate estimates of these parameters; along with dispersal, they govern population dynamics ( Lack 1954 ) and thus are essential for predicting population change and the effects of management actions. It can be frustrating, then, when survival is difficult to estimate for certain populations, as in some avian species that exhibit a substantial degree of dispersal.

Ecology↗

Pinyon and juniper encroachment into sagebrush ecosystems impacts distribution and survival of greater sage-grouse

In sagebrush ( Artemisia spp.) ecosystems, encroachment of pinyon ( Pinus spp.) and juniper ( Juniperus spp.; hereafter, “pinyon-juniper”) trees has increased dramatically since European settlement. Understanding the impacts of this encroachment on behavioral decisions, distributions, and population dynamics of greater sage-grouse (Centrocercus urophasianus) and other sagebrush obligate species could help benefit sagebrush ecosystem management actions. We employed a novel two-stage Bayesian model that linked avoidance across different levels of pinyon-juniper cover to sage-grouse survival. Our analysis relied on extensive telemetry data collected across 6 yr and seven subpopulations within the Bi-State Distinct Population Segment (DPS), on the border of Nevada and California. The first model stage indicated avoidance behavior for all canopy cover classes on average, but individual grouse exhibited a high degree of heterogeneity in avoidance behavior of the lowest cover class (e.g., scattered isolated trees). The second stage modeled survival as a function of estimated avoidance parameters and indicated increased survival rates for individuals that exhibited avoidance of the lowest cover class. A post hoc frailty analysis revealed the greatest increase in hazard (i.e., mortality risk) occurred in areas with scattered isolated trees consisting of relatively high primary plant productivity. Collectively, these results provide clear evidence that local sage-grouse distributions and demographic rates are influenced by pinyon-juniper, especially in habitats with higher primary productivity but relatively low and seemingly benign tree cover. Such areas may function as ecological traps that convey attractive resources but adversely affect population vital rates. To increase sage-grouse survival, our model predictions support reducing actual pinyon-juniper cover as low as 1.5%, which is lower than the published target of 4.0%. These results may represent effects of pinyon-juniper cover in areas with similar ecological conditions to those of the Bi-State DPS, where populations occur at relatively high elevations and pinyon-juniper is abundant and widespread.

Rangeland Ecology and Management↗

Monitoring trends in bat populations of the United States and territories: Problems and prospects

Bats are ecologically and economically important mammals. The life histories of bats (particularly their low reproductive rates and the need for some species to gather in large aggregations at limited numbers of roosting sites) make their populations vulnerable to declines. Many of the species of bats in the United States (U.S.) and territories are categorized as endangered or threatened, have been candidates for such categories, or are considered species of concern. The importance and vulnerability of bat populations makes monitoring trends in their populations a goal for their future management. However, scientifically rigorous monitoring of bat populations requires well-planned, statistically defensible efforts. This volume reports findings of an expert workshop held to examine the topic of monitoring populations of bats. The workshop participants included leading experts in sampling and analysis of wildlife populations, as well as experts in the biology and conservation of bats. Findings are reported in this volume under two sections. Part I of the report presents contributed papers that provide overviews of past and current efforts at monitoring trends in populations of bats in the U.S. and territories. These papers consider current techniques and problems, and summarize what is known about the status and trends in populations of selected groups of bats. The contributed papers in Part I also include a description of the monitoring program developed for bat populations in the United Kingdom, a critique of monitoring programs in wildlife in general with recommendations for survey and sampling strategies, and a compilation and analysis of existing data on trends in bats of the U.S. and territories. Efforts directed at monitoring bat populations are piecemeal and have shortcomings. In Part II of the report, the workshop participants provide critical analyses of these problems and develop recommendations for improving methods, defining objectives and priorities, gaining mandates, and enhancing information exchange to facilitate future efforts for monitoring trends in U.S. bat populations.

Information and Technology Report↗

Large-scale variation in wave attenuation of oyster reef living shorelines and the influence of inundation duration

One of the paramount goals of oyster reef living shorelines is to achieve sustained and adaptive coastal protection, which requires meeting ecological (i.e., develop a self-sustaining oyster population) and engineering (i.e., provide coastal defense) targets. In a large-scale comparison along the Atlantic and Gulf coasts of the United States, the efficacy of various designs of oyster reef living shorelines at providing wave attenuation was evaluated accounting for the ecological limitations of oysters with regard to inundation duration. A critical threshold for intertidal oyster reef establishment is 50% inundation duration. Living shorelines that spent less than one-half of the time (<50%) inundated were not considered suitable habitat for oysters, however, were effective at wave attenuation (68% reduction in wave height). Reefs that experienced >50% inundation were considered suitable habitat for oysters, but wave attenuation was similar to controls (no reef; ~5% reduction in wave height). Many of the oyster reef living shoreline approaches therefore failed to optimize the ecological and engineering goals. In both inundation regimes, wave transmission decreased with an increasing freeboard (difference between reef crest elevation and water level), supporting its importance in the wave attenuation capacity of oyster reef living shorelines. However, given that the reef crest elevation (and thus freeboard) should be determined by the inundation duration requirements of oysters, research needs to be refocused on understanding the implications of other reef parameters (e.g., width) for optimizing wave attenuation. A broader understanding of the reef characteristics and seascape contexts that result in effective coastal defense by oyster reefs is needed to inform appropriate design and implementation of oyster-based living shorelines globally.

Alabama, Florida, Louisiana, New Jersey, Virginia↗

Abundance of introduced species at home predicts abundance away in herbaceous communities

Many ecosystems worldwide are dominated by introduced plant species, leading to loss of biodiversity and ecosystem function. A common but rarely tested assumption is that these plants are more abundant in introduced vs. native communities, because ecological or evolutionary-based shifts in populations underlie invasion success. Here, data for 26 herbaceous species at 39 sites, within eight countries, revealed that species abundances were similar at native (home) and introduced (away) sites - grass species were generally abundant home and away, while forbs were low in abundance, but more abundant at home. Sites with six or more of these species had similar community abundance hierarchies, suggesting that suites of introduced species are assembling similarly on different continents. Overall, we found that substantial changes to populations are not necessarily a pre-condition for invasion success and that increases in species abundance are unusual. Instead, abundance at home predicts abundance away, a potentially useful additional criterion for biosecurity programmes.

Ecology Letters↗

Range-wide population trend analysis for greater sage-grouse (Centrocercus urophasianus)—Updated 1960–2021

Greater sage-grouse ( Centrocercus urophasianus ) are at the center of state and national land use policies largely because of their unique life-history traits as an ecological indicator for health of sagebrush ecosystems. This updated population trend analysis provides state and federal land and wildlife managers with best-available science to help guide current management and conservation plans aimed at benefitting sage-grouse populations. This analysis relied on previously published population trend modeling methodology from Coates and others (2021) and includes the addition of three analytical updates: (1) identification of population nadirs (lowest points within cycles) at the lek (breeding ground) and neighborhood cluster (group of leks) spatial scales, (2) truncation of prior distributions on rate of change in apparent abundance values to more realistic boundaries for leks with missing data, and (3) addition of 2 years of population lek count data (2020 and 2021) to the current dataset (1953–2021). Bayesian state-space models estimated 2.9 percent average annual decline in sage-grouse populations across their geographical range, which varied among subpopulations at the largest scale of analysis, termed climate clusters (2.2–4.6). Cumulative declines were 42.5, 65.6, and 80.1 percent range-wide across short (19 years), medium (35 years), and long (55 years) temporal periods, respectively. These results indicate that range-wide populations continued to decline during 2020 and 2021, although two climate clusters (eastern area and Bi-State area) have shown growth in population abundance in recent years, indicating they have surpassed a recent population abundance nadir.

Data Report↗

Using stable isotopes to investigate individual diet specialization in California sea otters (Enhydra lutris nereis)

Differences in diet composition among conspecifics (dietary specialization) have been documented across a broad range of taxonomic groups and habitats, and such variation at the individual level is increasingly recognized as an important component of diversity in trophic interactions. Accurate identification of individual dietary specialization, however, requires longitudinal dietary records that are labor-intensive and cost-prohibitive to obtain for many species. Here we explore the use of stable isotopes (δ 13 C and δ 15 N) as a promising technique for detecting and quantifying patterns of individual dietary specialization. Southern sea otters ( Enhydra lutris nereis ) offer a unique opportunity for testing this approach because (1) they consume a wide variety of prey that span multiple trophic levels, habitats, and ecologically defined functional groups; and (2) individual diet specialization can be validated with existing observational data. We analyzed the isotopic composition of sea otter vibrissae ( n = 31) in order to characterize inter- and intra-individual variation in sea otter diets at Monterey Bay, California, USA. At the population level, sea otters showed substantial variation in both δ 13 C and δ 15 N values, occupying nearly all of the “isotopic space” created by the diversity of isotopic signatures of potential prey taxa. Most of the variation in sea otter vibrissae was accounted for by differences between individuals, with much less contributed by within-individual variation. A majority of sea otters (∼80%) showed relatively little temporal variability in isotopic composition, suggesting that the proportional composition of most individuals' diets is relatively constant over time; a few individuals (∼20%) exhibited a high degree of intra-vibrissa isotopic variability, suggesting seasonal shifts in diet composition. These results and our interpretation of them were supported by long-term observational data on the diets of radio-tagged sea otters from the same population ( n = 23). Our results demonstrate that stable isotopes can provide an efficient tool for measuring individual- and population-level dietary breadth and may be useful for studying populations where longitudinal data on individuals would otherwise be impossible to acquire. This will be critical for examining the causes and consequences of dietary variation within and among consumer populations, thereby improving our understanding of these important ecological and evolutionary processes at the community level.

Ecology↗

Using spatial capture–recapture to elucidate population processes and space-use in herpetological studies

The cryptic behavior and ecology of herpetofauna make estimating the impacts of environmental change on demography difficult; yet, the ability to measure demographic relationships is essential for elucidating mechanisms leading to the population declines reported for herpetofauna worldwide. Recently developed spatial capture–recapture (SCR) methods are well suited to standard herpetofauna monitoring approaches. Individually identifying animals and their locations allows accurate estimates of population densities and survival. Spatial capture–recapture methods also allow estimation of parameters describing space-use and movement, which generally are expensive or difficult to obtain using other methods. In this paper, we discuss the basic components of SCR models, the available software for conducting analyses, and the experimental designs based on common herpetological survey methods. We then apply SCR models to Red-backed Salamander ( Plethodon cinereus ), to determine differences in density, survival, dispersal, and space-use between adult male and female salamanders. By highlighting the capabilities of SCR, and its advantages compared to traditional methods, we hope to give herpetologists the resource they need to apply SCR in their own systems.

Journal of Herpetology↗

Range-wide population trend analysis for greater sage-grouse (Centrocercus urophasianus)—Updated 1960–2022

Greater sage-grouse ( Centrocercus urophasianus ) are at the center of state and national land-use policies largely because of their unique life-history traits as an ecological indicator for health of sagebrush ecosystems. This updated population trend analysis provides state and federal land and wildlife managers with best-available science to help guide current management and conservation plans aimed at benefitting sage-grouse populations. This analysis relied on previously published population trend modeling methodology from Coates and others (2021, 2022a) and incorporated population lek count data through 2022. Bayesian state-space models estimated 2.9 percent average annual decline in sage-grouse populations across their geographical range, which varied among subpopulations at the largest scale of analysis, termed climate clusters (2.2–4.7). Cumulative declines were 40.9, 65.0, and 79.6 percent range-wide across short (19 years), medium (35 years), and long (55 years) temporal periods, respectively. These results indicate that the most recent nadir for range-wide populations occurred during 2021. However, growth during 2022 was modest, making 2021 a tentative final nadir at this point.

Data Report↗

Range-wide population trend analysis for greater sage-grouse (Centrocercus urophasianus)—Updated 1960–2023

Greater sage-grouse ( Centrocercus urophasianus ) are at the center of state and national land-use policies largely because of their unique life-history traits as an ecological indicator for health of sagebrush ecosystems. This updated population trend analysis provides state and federal land and wildlife managers with best-available science to help guide management and conservation plans aimed at benefitting sage-grouse populations. This analysis relied on previously published population trend modeling methodology from Coates and others (2021, 2022a) and incorporates population lek count data for 1960–2023. Included in this update are changes in terminology. Specifically, we now use the terms Period 1 (previously Long), Period 2 (previously Medium/Long), Period 3 (previously Medium), Period 4 (previously Short/Medium), Period 5 (previously Short), and Period 6 (previously Recent) to identify specific trends. State-space models estimated 2.8-percent average annual decline in sage-grouse populations between 1966 and 2021 (Period 1, six population oscillations) across their geographical range. Average annual decline among climate clusters for the same number of oscillations ranged between 2.1 and 3.1 percent. Cumulative declines were 41.1, 64.5, and 78.4 percent range-wide during Period 5 (19 years), Period 3 (35 years), and Period 1 (55 years), respectively. Population growth during 2022 and 2023 continue to point to 2021 as the most recent range-wide nadir.

Data Report↗