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Peter S. Coates

Publications and source records attributed to Peter S. Coates.

At least 73 records · Page 4Linked to original sources

Defining fine-scaled population structure among continuously distributed populations

Understanding wildlife population structure and connectivity can help managers identify conservation strategies, as structure can facilitate the study of population changes and habitat connectivity can provide information on dispersal and biodiversity. To facilitate the use of wildlife monitoring data for improved adaptive management, we developed a novel approach to define hierarchical tiers (multiple scales) of population structure. We defined population structure by combining graph theory with biological inference about dispersal capability (based on movement, gene flow, and habitat condition) and functional processes affecting movement (e.g. habitat selection across scales of landscape preferences). First, we developed least-cost paths between high fidelity sites (habitat patches) using a cost surface, informed from functional processes of habitat characteristics to account for resistance of inter-patch movements. Second, we combined the paths into a multi-path graph construct. Third, we used information on potential connectivity (dispersal distances) and functional connectivity (permeability of fragmented landscapes based on selection preferences) to decompose the graph into hierarchical tiers of connected subpopulations, denoting the degree that dispersal affected population structure. As a case study, we applied our approach across the greater sage-grouse ( Centrocercus urophasianus ) range, a species of conservation concern in western United States. We described the relative importance of local populations and where to potentially avoid landscape disturbances that may negatively affect population connectivity using centrality measures supported by graph theory, and we demonstrated close alignment of the resulting population structure with population densities. This method can be adapted for other species with site fidelity and used as a management tool to evaluate population trends and responses to landscape changes across different temporal and spatial scales.

Methods in Ecology and Evolution↗

Behavioral state-dependent habitat selection and implications for animal translocations

Post-release monitoring of translocated animals is often used to inform future translocation protocols. Quantifying habitat selection of translocated individuals may help identify features that characterize good settlement habitat and thus inform the choice of future release sites. However, translocated animals often undergo post-release behavioural modification, and their habitat selection may vary depending on the underlying behavioural state. To investigate this, we analysed behavioural state-dependent habitat selection in female greater sage-grouse Centrocercus urophasianus translocated from Wyoming to North Dakota, USA, using Hidden Markov Models combined with Integrated Step Selection Analysis. We segmented individual trajectories into behavioural phases corresponding to an exploratory state, characterized by broad and directed movements, and a restricted state, characterized by short and tortuous movements. Then, we quantified habitat selection in each state while accounting for seasonality and individual reproductive status. While in the exploratory state, sage-grouse exhibited natal habitat preference induction by selecting for high sagebrush cover, which is typical of their natal area in Wyoming but not of the release area in North Dakota. In the restricted state, sage-grouse selected for gentle topography and also adjusted their habitat selection to constraints imposed by seasonality and reproductive needs by selecting for high herbaceous cover during brood rearing. Synthesis and applications . Habitat selection of translocated sage-grouse differed between the post-release exploration and the settlement phase. Features selected after settling, not during exploration, are likely indicative of suitable settlement habitat. Our results suggest that areas characterized by gentle topography and high herbaceous cover are well-suited as release sites for sage-grouse translocated during the summer, especially brood-rearing females, and that sagebrush cover may not be a critical factor in determining the appropriateness of release sites for sage-grouse in North Dakota. Our findings highlight the need to consider behaviour when using habitat selection estimates to inform the choice of future release sites.

North Dakota, Wyoming↗

Offspring of translocated individuals drive the successful reintroduction of Columbian Sharp-tailed Grouse in Nevada, USA

Translocations of North American prairie-grouse (genus Tympanuchus ) present a conservation paradox wherein they are performed to augment, restore, or reintroduce populations, but translocated individuals exhibit a diminished ability to contribute to population restoration. For reintroduced populations without immigration, persistence can only be achieved through reproductive contributions by translocated individuals and their progeny. Due to the disruptive nature of translocation (e.g., physiological chronic stress), progeny produced at restoration sites may outperform founder populations in terms of demographics, but this hypothesis has yet to be tested. We reintroduced Columbian Sharp-tailed Grouse ( T. phasianellus columbianus ; CSTG) to north central Nevada from 2013 to 2017 and used integrated population models (IPMs) to evaluate the process of population establishment and estimate latent contributions of progeny hatched at the restoration site to population rate of change ( ⁠ λ ^ "> λ ^ ⁠ ). Specifically, we used annual lek (i.e. communal breeding arenas) counts and demographic data from translocated individuals to build two separate IPMs to estimate λ ^ "> λ ^ ⁠ . While keeping demographic contributions by translocated individuals identical between models, one IPM assumed local progeny performance was demographically similar to translocated individuals (i.e. the baseline-IPM), and the second assumed that local progeny performed demographically similar to non-translocated CSTG (i.e. the informative-IPM). The baseline-IPM predicted strong population declines following the conclusion of translocations and extirpation by 2020, and it failed to predict observed lek counts. Conversely, the informative-IPM predicted population growth rates ( ⁠ λ ^ "> λ ^ = 1.17, 95% credible interval [CI]: 0.74–1.50) that were more similar to field observations. Offspring of translocated individuals likely perform at similar levels to non-translocated populations, and by not accounting for demographic differences between translocated individuals and non-translocated progeny hatched at the restoration site, managers could underestimate population performance and persistence. Thus, translocation practices that maximize the number of offspring immediately recruited into restoration sites are likely to be the most successful.

Nevada↗

Individual variation in temporal dynamics of post-release habitat selection

Translocated animals undergo a phase of behavioral adjustment after being released in a novel environment, initially prioritizing exploration and gradually shifting toward resource exploitation. This transition has been termed post-release behavioral modification. Post-release behavioral modification may also manifest as changes in habitat selection through time, and these temporal dynamics may differ between individuals. We aimed to evaluate how post-release behavioral modification is reflected in temporal dynamics of habitat selection and its variability across individuals using a population of translocated female greater sage-grouse as a case study. Sage-grouse were translocated from Wyoming to North Dakota (USA) during the summers of 2018–2020. We analyzed individual habitat selection as a function of sagebrush cover, herbaceous cover, slope, and distance to roads. Herbaceous cover is a key foraging resource for sage-grouse during summer; thus, we expected a shift from exploration to exploitation to manifest as temporally-varying selection for herbaceous cover. For each individual sage-grouse ( N = 26), we tested two competing models: a null model with no time-dependence and a model with time-dependent selection for herbaceous cover. We performed model selection at the individual level using an information-theoretic approach. Time-dependence was supported for five individuals, unsupported for seven, and the two models were indistinguishable based on AIC c for the remaining fourteen. We found no association between the top-ranked model and individual reproductive status (brood-rearing or not). We showed that temporal dynamics of post-release habitat selection may emerge in some individuals but not in others, and that failing to account for time-dependence may hinder the detection of steady-state habitat selection patterns. These findings demonstrate the need to consider both temporal dynamics and individual variability in habitat selection when conducting post-release monitoring to inform translocation protocols.

Frontiers in Conservation Science↗

Field methods for translocating female greater sage-grouse (Centrocercus urophasianus) with their broods

Greater sage-grouse ( Centrocercus urophasianus ) have experienced considerable range contraction and reduced abundance in response to habitat loss and degradation. Translocation is a conservation action that is often used to reintroduce extirpated populations or augment existing small populations. Translocations have had limited success in restoring viable populations of sage-grouse; a lack of success is attributed to long-distance post-release movements away from release sites, reduced survival, and lack of reproductive success of translocated individuals. Translocating female sage-grouse with their chicks (brood translocation) is a technique aimed at promoting breeding area fidelity and reproduction and may be beneficial to population restoration efforts. Furthermore, the ability to capture, relocate, and release individuals while minimizing translocation-induced loss increases the overall probability of restoration success. Accordingly, we developed a protocol to translocate female sage-grouse and their broods simultaneously, using a delayed-release system that included a custom release box and acclimation pen. We tested our protocol across 2 separate restoration projects in North Dakota and California during 2017–2019 with a total of 38 translocated females and 196 chicks. We successfully released 174/196 chicks (88.8%) from 32/38 (84.2%) broods. Our protocol builds on existing translocation methods used to translocate sage-grouse and will likely prove to be a critical technique in restoring sage-grouse populations.

California, North Dakota, Wyoming↗

Sage-grouse population dynamics are adversely impacted by overabundant feral horses

In recent decades, feral horse ( Equus caballus ; horse) populations increased in sagebrush ( Artimesia spp.) ecosystems, especially within the Great Basin, to the point of exceeding maximum appropriate management levels (AML max ), which were set by land administrators to balance resource use by feral horses, livestock, and wildlife. Concomitantly, greater sage-grouse ( Centrocercus urophasianus ; sage-grouse) are sagebrush obligates that have experienced population declines within these same arid environments as a result of steady and continued loss of seasonal habitats. Although a strong body of research indicates that overabundant populations of horses degrade sagebrush ecosystems, empirical evidence linking horse abundance to sage-grouse population dynamics is missing. Within a Bayesian framework, we employed state-space models to estimate population rate of change ( λ ) using 15 years (2005–2019) of count surveys of male sage-grouse at traditional breeding grounds (i.e., leks) as a function of horse abundance relative to AML max and other environmental covariates (e.g., wildfire, precipitation, % sagebrush cover). Additionally, we employed a post hoc impact-control design to validate existing AML max values as related to sage-grouse population responses, and to help control for environmental stochasticity and broad-scale oscillations in sage-grouse abundance. On average, for every 50% increase in horse abundance over AML max , our model predicted an annual decline in sage-grouse abundance by 2.6%. Horse abundance at or below AML max coincided with sage-grouse λ estimates that were consistent with trends at non-horse areas elsewhere in the study region. Thus, AML max , as a whole, appeared to be set adequately in preventing adverse effects to sage-grouse populations. Results indicated 76%, 97%, and >99% probability of sage-grouse population decline relative to controls when horse numbers are 2, 2.5, and ≥3 times over AML max , respectively. As of 2019, horse herds exceeded AML max in Nevada, USA, by >4 times on average across all horse management areas. If feral horse populations continue to grow at current rates unabated, model projections indicate sage-grouse populations will be reduced within horse-occupied areas by >70.0% by 2034 (15-year projection), on average compared to 21.2% estimated for control sites. A monitoring framework that improves on estimating horse abundance and identifying responses of sage-grouse and other key indicator species (plant and animal) would be beneficial to guide management decisions that promote co-occurrence of horses with sensitive wildlife and livestock within landscapes subjected to multiple uses. Published 2021. This article is a U.S. Government work and is in the public domain in the USA. The Journal of Wildlife Management published by Wiley Periodicals LLC on behalf of The Wildlife Society.

Nevada↗

Large-scale wildfire reduces population growth in a peripheral population of sage-grouse

Drastic increases in wildfire size and frequency threaten western North American sagebrush ( Artemisia L. spp.) ecosystems. At relatively large spatial scales, wildfire facilitates type conversion of sagebrush-dominated plant communities to monocultures of invasive annual grasses ( e.g., Bromus tectorum L.). Annual grasses provide fine fuels that promote fire spread, contributing to a positive grass–fire feedback cycle that affects most sagebrush ecosystems, with expected habitat loss for resident wildlife populations. Greater sage-grouse ( Centrocercus urophasianus Bonaparte, 1827) are sagebrush obligate species that are indicators of sagebrush ecosystem function because they rely on different components of sagebrush ecosystems to meet seasonal life history needs. Because wildfire cannot be predicted, chronic impacts of wildfire on sage-grouse populations have been largely limited to correlative studies. Thus, evidence from well-designed experiments is needed to understand the specific mechanisms by which wildfire is detrimental to sage-grouse population dynamics.

California, Nevada↗

Health surveillance of a potential bridge host: Pathogen exposure risks posed to avian populations augmented with captive-bred pheasants

Augmentation of wild populations with captive-bred individuals presents an inherent risk of co-introducing novel pathogens to naïve species, but it can be an important tool for supplementing small or declining populations. Game species used for human enterprise and recreation such as the ring-necked pheasant ( Phasianus colchicus ) are commonly raised in captivity and released onto public and private wildlands as a method of augmenting naturalized pheasant populations. This study presents findings on pathogen exposure from three sources of serological data collected in California during 2014–2017 including (a) 71 pen-reared pheasants sampled across seven game bird breeding farms, (b) six previously released pen-reared pheasants captured at two study sites where wild pheasants occurred and (c) 79 wild pheasants captured across six study sites. In both pen-reared and wild pheasants, antibodies were detected against haemorrhagic enteritis virus (HEV), infectious laryngotracheitis (ILT), infectious bursal disease virus (IBDV), paramyxovirus type 1 (PMV-1) and Pasteurella multocida (PM). Previously released pen-reared pheasants were seropositive for HEV, ILT, and PM. Generalized linear mixed models accounting for intraclass correlation within groups indicated that pen-reared pheasants were more than twice as likely to test positive for HEV antibodies. Necropsy and ancillary diagnostics were performed in addition to serological testing on 40 pen-reared pheasants sampled from five of the seven farms. Pheasants from three of these farms tested positive by PCR for Siadenovirus, the causative agent of both haemorrhagic enteritis in turkeys and marble spleen disease of pheasants, which are serologically indistinguishable. Following necropsy, owners from the five farms were surveyed regarding husbandry and biosecurity practices. Farms ranged in size from 10,000 to more than 100,000 birds, two farms raised other game bird species on premises, and two farms used some form of vaccination. Biosecurity practices varied by farm, but the largest farm implemented the strictest practices.

California↗

Range-wide greater sage-grouse hierarchical monitoring framework—Implications for defining population boundaries, trend estimation, and a targeted annual warning system

Incorporating spatial and temporal scales into greater sage-grouse ( Centrocercus urophasianus ) population monitoring strategies is challenging and rarely implemented. Sage-grouse populations experience fluctuations in abundance that lead to temporal oscillations, making trend estimation difficult. Accounting for stochasticity is critical to reliably estimate population trends and investigate variation related to deterministic factors on the landscape, which are amenable to management action. Here, we describe a novel, range-wide hierarchical monitoring framework for sage-grouse centered on four objectives: (1) create a standardized database of lek counts, (2) develop spatial population structures by clustering leks, (3) estimate spatial trends at different temporal extents based on abundance nadirs (troughs), and (4) develop a targeted annual warning system to help inform management decisions. Using automated and repeatable methods (software), we compiled a lek database (as of 2019) that contained 262,744 counts and 8,421 unique lek locations from disparate state data. The hierarchical population units (clusters) included 13 nested levels, identifying biologically relevant units and population structure that minimized inter-cluster sage-grouse movements. With these products, we identified spatiotemporal variation in trends in population abundance using Bayesian state-space models. We estimated 37.0, 65.2, and 80.7-percent declines in abundance range-wide during short (17 years), medium (33 years), and long (53 years) temporal scales, respectively. However, some areas exhibited evidence of increasing trends in abundance in recent decades. Models predicted 12.3, 19.2, and 29.6 percent of populations (defined as clusters of neighboring leks) consisted of over 50-percent probability of extirpation at 19, 38, and 56-year projections from 2019, respectively, based on averaged annual rate of change in apparent abundance across two, four, and six oscillations (average period of oscillation is 9.4 years). At the lek level, models predicted 45.7, 60.1, and 78.0 percent of leks with over 50-percent extirpation probabilities over the same time periods, respectively, mostly located on the periphery of the species’ range. The targeted annual warning system automates annual identification of local populations exhibiting asynchronous decline relative to regional population patterns using simulated management actions and an optimization algorithm for evaluating range-wide stabilization of population abundance. In 2019, approximately 3.2 percent of leks and 2.0 percent of populations were identified by the targeted annual warning system for management intervention range-wide.

California, Colorado, Idaho, Montana, Nevada, Nort↗

Nesting, brood rearing, and summer habitat selection by translocated greater sage‐grouse in North Dakota, USA

Human enterprise has led to large‐scale changes in landscapes and altered wildlife population distribution and abundance, necessitating efficient and effective conservation strategies for impacted species. Greater sage‐grouse ( Centrocercus urophasianus ; hereafter sage‐grouse) are a widespread sagebrush ( Artemisia spp.) obligate species that has experienced population declines since the mid‐1900s resulting from habitat loss and expansion of anthropogenic features into sagebrush ecosystems. Habitat loss is especially evident in North Dakota, USA, on the northeastern fringe of sage‐grouse’ distribution, where a remnant population remains despite recent development of energy‐related infrastructure. Resource managers in this region have determined a need to augment sage‐grouse populations using translocation techniques that can be important management tools for countering species decline from range contraction. Although translocations are a common tool for wildlife management, very little research has evaluated habitat following translocation, to track individual behaviors such as habitat selection and fidelity to the release site, which can help inform habitat requirements to guide selection of future release sites. We provide an example where locations from previously released radio‐marked sage‐grouse are used in a resource selection function framework to evaluate habitat selection following translocation and identify areas of seasonal habitat to inform habitat management and potential restoration needs. We also evaluated possible changes in seasonal habitat since the late 1980s using spatial data provided by the Rangeland Analysis Platform coupled with resource selection modeling results. Our results serve as critical baseline information for habitat used by translocated individuals across life stages in this study area, and will inform future evaluations of population performance and potential for long‐term recovery.

Montana, North Dakota, South Dakota, Wyoming↗

Synthesizing and analyzing long-term monitoring data: A greater sage-grouse case study

Long-term monitoring of natural resources is imperative for increasing the understanding of ecosystem processes, services, and how to manage those ecosystems to maintain or improve function. Challenges with using these data may occur because methods of monitoring changed over time, multiple organizations collect and manage data differently, and monetary resources fluctuate, affecting many aspects of data. Because many species respond to changes in habitat conditions and predator-prey relationships across different spatial scales that span management boundaries, greater efforts for collaborating are essential. We demonstrate the challenges and methods for standardizing greater sage-grouse ( Centrocercus urophasianus ) long-term monitoring data across the species range in the western United States to inform population modeling needs identified by the Western Association of Fish and Wildlife Agencies. We used automated and repeatable methods of standardizing data via custom open-source software ( grsg_lekdb ) to improve the scientific integrity of future sage-grouse population assessments within and among states. Data standardization included reconciling uses of different terminology and expunging unusable data, resulting in the removal of 26% of data records due to database insertion errors and modifications to >1 million values to correct formatting and typing errors. Our approaches maximized the inclusion of usable data and identified data that could inform detection probabilities, population trends, and monitoring guidelines. Using sage-grouse databases as an example, we identified the importance of data management and how quality assurance and quality control measures can improve the usefulness of these data for future research needs. Our methods of using informatics and concluding recommendations can support similar endeavors of flora and fauna monitoring programs, whether those efforts are to use existing data or support new monitoring programs.

Ecological Informatics↗

Free-roaming horses disrupt greater sage-grouse lekking activity in the Great Basin

Greater Sage-Grouse ( Centrocercus urophasianus; hereafter, sage-grouse) and free-roaming horses ( Equus caballus ) co-occur within large portions of sagebrush ecosystems within the Great Basin of western North America. In recent decades, sage-grouse populations have declined substantially while concomitant free-roaming horse populations have increased drastically. Although multiple studies have reported free-roaming horses adversely impacting native ungulate species, direct interactions between free-roaming horses and sage-grouse have not been documented previously. We compiled sage-grouse lek count data and associated ungulate observations during spring of 2010 and 2013–2018. We used Bayesian multinomial logistic models to examine the response of breeding male sage-grouse to the presence of native (i.e. mule deer, pronghorn) and non-native (i.e. cattle, free-roaming horses) ungulates on active sage-grouse leks (traditional breeding grounds). We found sage-grouse were approximately five times more likely to be present on active leks concurrent with native ungulates compared to non-native ungulates. Of the four different ungulate species, sage-grouse were least likely to be at active leks when free-roaming horses were present. Our results indicate that free-roaming horse presence at lek sites negatively influences sage-grouse lekking activity. Because sage-grouse population growth is sensitive to breeding success, disruption of leks by free-roaming horses could reduce breeding opportunities and limit breeding areas within sage-grouse habitat.

California, Idaho, Nevada, Oregon, Utah↗

A customized framework for regional classification of conifers using automated feature extraction

Pinyon and juniper expansion into sagebrush ecosystems is one of the major challenges facing land managers in the Great Basin. Effective pinyon and juniper treatment requires maps that accurately and precisely depict tree location and degree of woodland development so managers can target restoration efforts for early stages of pinyon and juniper expansion. However, available remotely sensed layers that cover a regional spatial extent lack the spatial resolution or accuracy to meet this need. Accuracy can be improved using object-based image analysis methods such as automated feature extraction, which has proven successful in accurately classifying land cover at the site-level but to date has yet to be applied to regional extents due to time and computational limitations. Using Feature Analyst™, we implement our framework with 1-m 2 reference imagery provided by National Agricultural Imagery Program to classify conifers across Nevada and northeastern California. Our resulting binary conifer map has an overall accuracy of 86%. We discuss the advantages to accuracy and precision our framework provides compared to other classification methods

Oregon, California, Nevada, Utah↗

Ecological correlates of fecal corticosterone metabolites in female Greater Sage-Grouse (Centrococercus urophasianus)

Measurement of physiological responses can reveal effects of ecological conditions on an animal and correlate with demographic parameters. Ecological conditions for many animal species have deteriorated as a function of invasive plants and habitat fragmentation. Expansion of juniper (Juniperus spp.) trees and invasion of annual grasses into sagebrush (Artemisia spp.) ecosystems have contributed to habitat degradation for Greater Sage-Grouse (Centrococercus urophasianus (Bonaparte, 1827); hereafter, “Sage-Grouse”), a species of conservation concern throughout its range. We evaluated relationships between habitat use in a landscape modified by juniper expansion and annual grasses and corticosterone metabolite levels (stress responses) in feces (FCORTm) of female Sage-Grouse. We used remotely sensed data to estimate vegetation cover within hens’ home ranges and accounted for factors that influence FCORTm in other vertebrates, such as age and weather. We collected 36 fecal samples from 22 radio-collared hens during the brood-rearing season (24 May–26 July) in southwestern Idaho 2017–18. Concentrations of corticosterone increased with home range size but decreased with reproductive effort and temperature. The importance of home range size suggests that maintaining or improving habitats that promote smaller home ranges would likely facilitate a lower stress response by hens, which should benefit Sage-Grouse survival and reproduction.

Idaho↗

A rapid assessment function to estimate common raven population densities: Implications for targeted management

Common raven ( Corvus corax ; raven) populations have increased over the past 5 decades within the western United States. Raven population increases have been largely attributed to growing resource subsidies from expansion of human enterprise. Concomitantly, managers are becoming increasingly concerned about elevated adverse effects on multiple sensitive prey species, damage to livestock and agriculture, and human safety. Managers could benefit from a rapid but reliable method to estimate raven densities across spatiotemporal scales to monitor raven populations more efficiently and inform targeted and adaptive management frameworks. However, obtaining estimates of raven density is data- and resource-intensive, which renders monitoring within an adaptive framework unrealistic. To address this need, we developed a rapid survey protocol for resource managers to estimate site-level density based on the average number of ravens per survey. Specifically, we first estimated raven densities at numerous field sites with robust distance sampling procedures and then used regression to investigate the relationship between those density estimates and the number of ravens per survey, which revealed a strong correlation ( R 2 = 0.86). For management application, we provide access to R function software through a web-based interface to estimate density using number of ravens per survey, which we refer to as a Rapid Assessment Function (RAF). Then, using a simulation analysis of data from sites with abundant surveys and the RAF, we estimated raven density based on different numbers of surveys to help inform how many surveys are needed to achieve reliable estimates within this rapid assessment. While more robust procedures of distance sampling are the preferred methods for estimating raven densities from count surveys, the RAF tool presented herein provides a reliable approximation for informing management decisions when managers are faced with resource and small sample size constraints.

California, Idaho, Nevada, Oregon↗

Occurrence, resource use, and demography of the common raven in North America: A research synthesis

We reviewed the scientific literature to inventory existing studies of common raven ( Corvus corax ; raven) ecology in western North America. We conducted an intial literature review between June 2015 and March 2018. Prior to completing our review, we revisited the published literature for any additional relevant studies in July 2021. Our goal was to identify knowledge gaps and to synthesize the current understanding of environmental features that may support raven populations that pose general threats to biodiversity and sensitive species in particular. We focused our review on studies with direct conservation applications related to 3 processes of raven ecology: occurrence, resource use, and demography. We identified covariates that researchers associated with these processes of raven ecology, and we also quantified the geographic distribution of studies. Our review identified 54 studies, with an increasing number of studies published per decade and a geographic bias characterized by more studies conducted in the Mojave and Columbia Plateau ecoregions than elsewhere. Most studies (44) reported on a single ecological process, but 10 studies reported on multiple ecological processes. Results related to raven occurrence appeared 31 times; demographic results appeared 21 times; and resource use was reported 17 times. We also identified 13 explanatory covariates regularly invoked to explain variation in raven ecological processes. Greater attention was given to covariates including vegetation land cover, human settlement, recreation, and linear rights-of-ways than were used to explain variation in ecological processes. Most demographic studies investigated raven reproduction exclusively, but a small number of studies considered raven survival exclusively or in combination with reproduction. Along with a detailed summary of individual studies provided as an appendix, we intend for our findings to serve as a reference and to help identify future research priorities.

Human–Wildlife Interactions↗

Synthesis of nest predation impacts of common ravens on sensitive avian species

Decades of mounting scientific evidence have revealed that common raven ( Corvus corax ; raven) population numbers have been increasing across nearly all regions of their geographic range in North America. Concomitantly, numerous native wildlife species have experienced elevated predation rates from ravens as populations have increased and expanded their range. Managers are concerned that increased raven predation of many threatened and endangered avian species in the U.S. and Canada during nesting periods may be hampering species recovery. We explored the literature to aggregate existing knowledge and evaluate the impacts of raven predation on nests and young of sensitive avian species. We used this information to develop a simple relative index for each species, the “Raven Impact Index” (RII). The RII incorporated the species demographic rates, abundance of ravens in relation to each sensitive species’ breeding range, and the degree of overlap between raven and sensitive prey distributions. We also developed a second relative descriptor describing our confidence in each RII, termed a “Impact Credibility Index (ICI).” The species ICI was based on the number of published studies and the type of evidence presented (e.g., circumstantial vs. direct). We found evidence of nest predation on 8 sensitive avian species and suspected nest predation on 1 additional species. All species shared aspects of nesting biology that suggested they would likely be susceptible to raven nest predation. The RII varied among prey species, with greater sage-grouse ( Centrocercus urophasianus ) having the highest relative impact values, followed by snowy plover ( Charadrius nivosus nivosus ), marbled murrelet ( Brachyramphus marmoratus ), and Gunnison sage-grouse ( Centrocercus minimus ). Our species RII is intended to inform management decisions regarding actions that mitigate the negative effects of raven predation of sensitive avian species. Although elevated nest predation may be of high conservation concern, it is important to recognize that all of the sensitive native prey species we established an RII for also face multiple conservation threats.

Human–Wildlife Interactions↗

SMaRT: A science-based tiered framework for common ravens

Large-scale increases and expansion of common raven ( Corvus corax ; raven) populations are occurring across much of North America, leading to increased negative consequences for livestock and agriculture, human health and safety, and sensitive species conservation. We describe a science-based adaptive management framework that incorporates recent quantitative analyses and mapping products for addressing areas with elevated raven numbers and minimizing potential adverse impacts to sensitive species, agricultural damage, and human safety. The framework comprises 5 steps: (1) desktop analysis; (2) field assessments; (3) comparison of raven density estimates to an ecological threshold (in terms of either density or density plus distance to nearest active or previous nest); (4) prescribing management options using a 3-tiered process (i.e., habitat improvements, subsidy reductions, and direct actions using StallPOPd.V4 software); and (5) post-management monitoring. The framework is integrated within the Science-based Management of Ravens Tool (SMaRT), a web-based application outfitted with a user-friendly interface that guides managers through each step to develop a fully customized adaptive plan for raven management. In the SMaRT interface, users can: (1) interact with pre-loaded maps of raven occurrence and density and define their own areas of interest within the Great Basin to delineate proposed survey or treatment sites; (2) enter site-level density estimates from distance sampling methods or perform estimation of raven densities using the rapid assessment protocol that we provide; (3) compare site-level density estimates to an identified ecological threshold; and (4) produce a list of potential management options for their consideration. The SMaRT supports decision-making by operationalizing scientific products for raven management and facilitates realization of diverse management goals including sensitive species conservation, protection of livestock and agriculture, safeguarding human health, and addressing raven overabundance and expansion. We illustrate the use of the framework through SMaRT using an example of greater sage-grouse ( Centrocercus urophasianus ) conservation efforts within the Great Basin, USA.

California, Idaho, Nevada, Oregon, Utah↗