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At least 847 records · Page 47Linked to original sources

Avian movements and wetland connectivity in landscape conservation

The current conservation crisis calls for research and management to be carried out on a long-term, multi-species basis at large spatial scales. Unfortunately, scientists, managers, and agencies often are stymied in their effort to conduct these large-scale studies because of a lack of appropriate technology, methodology, and funding. This issue is of particular concern in wetland conservation, for which the standard landscape approach may include consideration of a large tract of land but fail to incorporate the suite of wetland sites frequently used by highly mobile organisms such as waterbirds (e.g., shorebirds, wading birds, waterfowl). Typically, these species have population dynamics that require use of multiple wetlands, but this aspect of their life history has often been ignored in planning for their conservation. We outline theoretical, empirical, modeling, and planning problems associated with this issue and suggest solutions to some current obstacles. These solutions represent a tradeoff between typical in-depth single-species studies and more generic multi-species studies. They include studying within- and among-season movements of waterbirds on a spatial scale appropriate to both widely dispersing and more stationary species; multi-species censuses at multiple sites; further development and use of technology such as satellite transmitters and population-specific molecular markers; development of spatially explicit population models that consider within-season movements of waterbirds; and recognition from funding agencies that landscape-level issues cannot adequately be addressed without support for these types of studies.

Conservation Biology↗

Mourning dove hunting regulation strategy based on annual harvest statistics and banding data

Although managers should strive to base game bird harvest management strategies on mechanistic population models, monitoring programs required to build and continuously update these models may not be in place. Alternatively, If estimates of total harvest and harvest rates are available, then population estimates derived from these harvest data can serve as the basis for making hunting regulation decisions based on population growth rates derived from these estimates. I present a statistically rigorous approach for regulation decision-making using a hypothesis-testing framework and an assumed framework of 3 hunting regulation alternatives. I illustrate and evaluate the technique with historical data on the mid-continent mallard (Anas platyrhynchos) population. I evaluate the statistical properties of the hypothesis-testing framework using the best available data on mourning doves (Zenaida macroura). I use these results to discuss practical implementation of the technique as an interim harvest strategy for mourning doves until reliable mechanistic population models and associated monitoring programs are developed.

Journal of Wildlife Management↗

Estimating numbers of greater prairie-chickens using mark-resight techniques

Current monitoring efforts for greater prairie-chicken (Tympanuchus cupido pinnatus) populations indicate that populations are declining across their range. Monitoring the population status of greater prairie-chickens is based on traditional lek surveys (TLS) that provide an index without considering detectability. Estimators, such as immigration-emigration joint maximum-likelihood estimator from a hypergeometric distribution (IEJHE), can account for detectability and provide reliable population estimates based on resightings. We evaluated the use of mark-resight methods using radiotelemetry to estimate population size and density of greater prairie-chickens on 2 sites at a tallgrass prairie in the Flint Hills of Kansas, USA. We used average distances traveled from lek of capture to estimate density. Population estimates and confidence intervals at the 2 sites were 54 (CI 50-59) on 52.9 km 2 and 87 (CI 82-94) on 73.6 km2. The TLS performed at the same sites resulted in population ranges of 7-34 and 36-63 and always produced a lower population index than the mark-resight population estimate with a larger range. Mark-resight simulations with varying male:female ratios of marks indicated that this ratio was important in designing a population study on prairie-chickens. Confidence intervals for estimates when no marks were placed on females at the 2 sites (CI 46-50, 76-84) did not overlap confidence intervals when 40% of marks were placed on females (CI 54-64, 91-109). Population estimates derived using this mark-resight technique were apparently more accurate than traditional methods and would be more effective in detecting changes in prairie-chicken populations. Our technique could improve prairie-chicken management by providing wildlife biologists and land managers with a tool to estimate the population size and trends of lekking bird species, such as greater prairie-chickens.

Journal of Wildlife Management↗

Estimation and confidence intervals for empirical mixing distributions

Questions regarding collections of parameter estimates can frequently be expressed in terms of an empirical mixing distribution (EMD). This report discusses empirical Bayes estimation of an EMD, with emphasis on the construction of interval estimates. Estimation of the EMD is accomplished by substitution of estimates of prior parameters in the posterior mean of the EMD. This procedure is examined in a parametric model (the normal-normal mixture) and in a semi-parametric model. In both cases, the empirical Bayes bootstrap of Laird and Louis (1987, Journal of the American Statistical Association 82, 739-757) is used to assess the variability of the estimated EMD arising from the estimation of prior parameters. The proposed methods are applied to a meta-analysis of population trend estimates for groups of birds.

Biometrics↗

Lack of association among duck broodmates during migration and wintering

Male (Lensink, 1964: 19) and female ducks tend to return to the area where they last bred or were raised (Sowles, 1955). Band recovery data show a similar tendency for ducks to return to wintering areas (Stewart et al., 1958; Martinson, 1966). Wintering British Columbia Mallard ( Anas platyrhynchos ) populations may be definite associations of birds that breed in the same general locality, migrate together, and use the same wintering area (Munro, 1943). On the other hand Gollop (1965: 36-37) showed that Mallards reared in Saskatchewan or breeding there re- turned in subsequent years, but "neither migrated nor wintered as definite associations." He based his conclusions on recovery data from groups of Mallards banded on the same slough and from broodmates. His data showed, by date or area of recovery, that the birds migrated independently and sometimes to different wintering localities. This paper presents additional data suggesting that ducks banded as brood- mates may migrate independently.

The Auk↗

Evaluating models of population process in a threatened population of Steller’s eiders: A retrospective approach

The Alaskan breeding population of Steller’s eiders ( Polysticta stelleri ) was listed as threatened under the Endangered Species Act in 1997 in response to perceived declines in abundance throughout their breeding and nesting range. Aerial surveys suggest the breeding population is small and highly variable in number, with zero birds counted in 5 of the last 25 years. Research was conducted to evaluate competing population process models of Alaskan-breeding Steller’s eiders through comparison of model projections to aerial survey data. To evaluate model efficacy and estimate demographic parameters, a Bayesian state-space modeling framework was used and each model was fit to counts from the annual aerial surveys, using sequential importance sampling and resampling. The results strongly support that the Alaskan breeding population experiences population level nonbreeding events and is open to exchange with the larger Russian-Pacific breeding population. Current recovery criteria for the Alaskan breeding population rely heavily on the ability to estimate population viability. The results of this investigation provide an informative model of the population process that can be used to examine future population states and assess the population in terms of the current recovery and reclassification criteria.

Open-File Report↗

Age and colony variation in Adélie penguin metapopulation vital rates: Insights from a 25-year mark–recapture study

Understanding how vital rates vary with age, life-history stage, and among populations is fundamental for predicting the demographic consequences of environmental change, especially in longer-lived species with complex life histories. These species often exhibit delayed maturity and iteroparity, making nuanced demographic insights critical for assessing their long-term viability. This study investigated age- and colony-related variation in Adélie penguin vital rates including survival, recruitment, and breeding propensity. We used mark–recapture data collected over 25 years (1996–2020) from three Adélie penguin breeding colonies that differed in population sizes and trends but comprised a metapopulation located at capes Royds, Bird, and Crozier on Ross Island, Antarctica. We used multi-state models to estimate survival and detection rates relative to reproductive state and breeding colony and estimated transition probabilities reflecting movements between reproductive states and colonies. Apparent survival varied by reproductive state, colony, and age and averaged 0.80 (SD = 0.02) at Bird, and 0.72 (SD = 0.03) and 0.73 (SD = 0.03) at Crozier and Royds, respectively, for pre-breeders age 2–7 years with strong declines in pre-breeder survival after age 8. We observed less age-related variation in survival of breeders and non-breeders, but we observed differences between colonies with lower survival for breeders (0.72 to 0.80) compared to non-breeders (0.75 to 0.82). The average probability of surviving the first 2 years after fledging ranged from 0.43 (SD = 0.14) at Royds and Crozier (0.43, SD = 0.10) to 0.55 (SD = 0.15) at Bird. Movement between colonies was highest for pre-breeders (0.00%–12.00% depending on age and colony) and lowest for breeders (<0.20%). We observed the lowest age-related recruitment rates at Royds, with recruitment at Crozier almost twice as high, and intermediate at Bird. Breeding propensity was highest at Crozier and lowest at Bird. Colony-specific variation in vital rates likely contributed differently to population trajectories, suggesting that care must be taken to extrapolate vital rate estimates across colonies even within a metapopulation. These findings also highlight the importance of considering age, life-history stage, and geographic variation when assessing population vital rates in species with complex life histories.

Frontiers in Ecology and Environment↗

Variation in age ratio of midcontinent greater white-fronted geese during fall migration

Annual productivity is an important parameter for the management of waterfowl populations. Fall age ratio (juveniles:total birds) is an index of productivity of the preceding breeding season. However, differences in the timing of migration between family groups and nonbreeding birds may bias age-ratio estimates. We examined temporal variation in age ratios of midcontinent greater white-fronted geese Anser albifrons frontalis from interior and northwestern Alaska at a northern autumn staging area near Delta Junction, Alaska. Photographic sampling conducted near Delta Junction resulted in an annual age ratio of 0.388 ± 0.004 (mean ± SE) in 2010 and 0.390 ± 0.001 in 2011. Our study demonstrated temporal variation in age ratios over the duration of the migration period during August and September. We recommend that sampling be conducted for 3-d periods at the beginning, middle, and end of the migration period to account for temporal variation in migration of family groups.

Journal of Fish and Wildlife Management↗

Grazing intensity effects on the breeding avifauna of North Dakota native grasslands

A breeding bird census and plant survey was conducted on 180 samples of lightly, moderately, and heavily grazed and hayed native grasslands in North Dakota in 1974. The ten most important cover plants on each of eight major physiographic landforms in three of the four regions (the Agassiz Lake Plain excluded) overlapped so extensively that only 19 species were involved: 13 grasses or sedges, four forbs, one shrub, and one clubmoss. Bird densities were generally highest in (i) regions and landforms containing numerous natural basin wetlands, (ii) flatter, glaciated landforms containing more fertile soils, and (iii) landforms of greater relief and high habitat heterogeneity. Avian species richness tended to decrease with increased grazing intensity, but total bird density increased due to higher populations of a few species, and hayland that had been mowed and raked during the previous growing season was highly attractive to some species.

Canadian Field-Naturalist↗

California condors

The California condor ( Gymnogyps californianus ) is a member of the vulture family. With a wingspan of about 3 m (9 ft) and weighing about 9 kg (20 lb), it spends much of its time in soaring flight visually seeking dead animals as food. The California condor has always been rare (Wilbur 1978; Pattee and Wilbur 1989). Although probably numbering in the thousands during the Pleistocene epoch in North America, its numbers likely declined dramatically with the extinction of most of North America's large mammals 10,000 years ago. Condors probably numbered in the hundreds and were nesting residents in British Columbia, Washington, Oregon, California, and Baja California around 1800. In 1939 the condor population was estimated at 60-100 birds, and its home range was reduced to the mountains and foothills of California, south of San Francisco and north of Los Angeles. Conservation to halt the condor's decline included establishing the Sisquoc (1937) and Sespe (1947) condor sanctuaries within the Los Padres National Forest, obtaining fully protected status under California Fish and Game Code (1953), placement on California's first state endangered species list (1971), and, finally, being listed by the federal government under the Endangered Species Act of 1973 (Wilbur 1978). The success of these efforts could not be judged, however, because verifiable status and trends data did not become available until 1982. By using these data, we confirmed the decline in condor numbers over the past 50 years was even greater than thought.

Book chapter↗

Changing land use: Problems and opportunities

Under the pressure of increasing human populations and expanding demands for food and fiber, native tropical and temperate habitats are becoming more restricted, and populations of many resident and migratory birds are declining. Mist net surveys of 111 forest and agricultural sites in Mexico, Belize, and Guatemala show that some migratory species use a wide variety of habitats during the non-breeding season; other migrants, especially ground-feeding insectivores that nest in temperate forests, are largely restricted to forest habitats during the northern winter. Most tropical residents are also scarce or absent in agricultural habitats; this is especially true of the suboscine families, which are an important component of tropical forests: Furnariidae, Dendrocolaptidae, Formicariidae, Tyrannidae, and Pipridae: Of the various agricultural habitats studied, arboreal crops, especially mature citrus and cacao, were used by a wide variety and relatively large number of migrants; at the other extreme, few birds were captured or observed in commercially grown allspice and platanos (bananas). Although habitat constraints on many species are increasing, the impact of these constraints can be reduced through research, management, legislation, and especially education. Long-range habitat management objectives that reduce forest fragmentation and promote retention of critical habitats for species can be realized if an informed and concerned public can be created

Book chapter↗

Invasive herbivory: resident Canada geese and the decline of wild rice along the tidal Patuxent River

While concern grows over the increasing numbers of exotic mute swans ( Cygnus olor ) on the Chesapeake Bay, less attention seems to be given to the highly familiar and native Canada goose ( Branta canadensis ) which has over time developed unprecedented nonmigratory, or resident, populations. Although nuisance flocks of Canada geese have been well advertised at city parks, athletic fields, and golf courses over the past three decades, recent expansion of populations to an estimated one million birds in the Atlantic Flyway, and to over 100,000 in Maryland, carries a threat of broader ecological consequences.

Maryland↗

Eastern Imperial Eagle Aquila heliaca

Eastern imperial eagles are a short-, medium-distance, partially-migratory, or even non-migratory, raptor that breeds at the forest-steppe interface in Eurasia and winters in Northern Africa, the Middle East or South Asia. Migratory strategies of imperial eagles are diverse. Eagles breeding in Central and Southeast Europe and south of the Black Sea usually are year-round residents or partial- or short- distance migrants that winter in the Balkan Peninsula, Northern Africa, or western parts of the Middle East. Eagles that summer to the east of the Black Sea are usually medium-distance migrants that winter in the Middle East or south Asia. Migration tends to follow topographic features, avoids water-crossings and, especially for young birds, may be intermittent and indirect. Populations of imperial eagles are small, in decline in some parts of the distribution, and the species faces a large number of threats including electrocution, persecution, and capture for sale in markets.

Book chapter↗

Framework for assessing and mitigating the impacts of offshore wind energy development on marine birds

Offshore wind energy development (OWED) is rapidly expanding globally and has the potential to contribute significantly to renewable energy portfolios. However, development of infrastructure in the marine environment presents risks to wildlife. Marine birds in particular have life history traits that amplify population impacts from displacement and collision with offshore wind infrastructure. Here, we present a broadly applicable framework to assess and mitigate the impacts of OWED on marine birds. We outline existing techniques to quantify impact via monitoring and modeling (e.g., collision risk models, population viability analysis), and present a robust mitigation framework to avoid, minimize, or compensate for OWED impacts. Our framework addresses impacts within the context of multiple stressors across multiple wind energy developments. We also present technological and methodological approaches that can improve impact estimation and mitigation. We highlight compensatory mitigation as a tool that can be incorporated into regulatory frameworks to mitigate impacts that cannot be avoided or minimized via siting decisions or alterations to OWED infrastructure or operation. Our framework is intended as a globally-relevant approach for assessing and mitigating OWED impacts on marine birds that may be adapted to existing regulatory frameworks in regions with existing or planned OWED.

Biological Conservation↗

A review of the ecology and conservation biology of Sali (Micronesian Starling, Aplonis opaca guami) on Guam

The accidental introduction of the Brown Treesnake (BTS, Boiga irregularis ) to Guam following World War II led to the extinction, extirpation, or severe decline of most of Guam’s native avifauna. One forest bird species that managed to persist is the cavity-nesting Såli (Micronesian Starling, Aplonis opaca guami ), a once-ubiquitous native omnivore whose current Guam distribution is restricted primarily to urbanized areas in the northern half of the island, with a second much smaller population on Cocos Island off southern Guam. Såli on Guam breed year-round and are habitat generalists with large home ranges. Besides arthropods and small vertebrates, they consume fruit from a wide range of native and introduced plant species and are key seed dispersers within the local ecosystem. Såli on Guam suffer extremely high post-fledging mortality due to predation by BTS and cats, leading to a population age structure strongly skewed towards adult birds. Other threats include habitat loss and degradation, extreme weather events, and sea level rise. Key management activities aimed at restoring this species include predator control, while non-native ungulate removal and vegetation management may be undertaken to support broader ecological recovery. This species account on Såli provides a review of the literature on this species, synthesizing information on habitat use, life history, and demographics to provide a biological foundation for future recovery efforts.

Micronesica↗

An assessment of arthropod prey resources at Nakula Natural Area Reserve, a potential site of reintroduction for Kiwikiu (Pseudonestor xanthophrys) and Maui `Alauahio (Parareomyza montana)

Hawaiian forest birds have declined dramatically since humans arrived in the archipelago. Birds from all foraging guilds have been affected but insectivorous species are currently at greatest risk of extinction. On the island of Maui, populations and ranges of the insectivorous kiwikiu (Maui parrotbill; Pseudonestor xanthophrys) and Maui &lsquo;alauahio (Maui creeper; Paroreomyza montana) have declined significantly from historic levels primarily due to habitat loss, predation,disease, and food web disruption, leading to federal listings of endangered species and species of concern, respectively. Recovery plans for these birds include reestablishment of populations in parts of their former range. Nakula Natural Area Reserve on the leeward side of HaleakalāVolcano has been targeted for release of wild-caught or captive-bred individuals. The mesic, montane koa-&lsquo;ōhi&lsquo;a (Acacia koa-Metrosideros polymorpha) forest at Nakula has been heavily impacted through grazing by feral ungulates, but recent management actions to exclude these animals are promoting forest recovery. The objective of this study was to assess the arthropod prey base at Nakula in preparation for reintroductions of kiwikiu and Maui &lsquo;alauahio. To accomplish that goal, we compared arthropod abundances at Nakula to those at Hanawi Natural Area Reserve and Waikamoi Preserve, areas where kiwikiu and Maui &lsquo;alauahio are currently found. We also identified diets of kiwikiu and Maui &lsquo;alauahio from fecal samples to better understand and evaluate the prey base at Nakula. Assessment methods included clipping branch tips to sample arthropods within the foliage of koa and &lsquo;ōhi&lsquo;a, using traps to quantify arthropods on koa and &lsquo;ōhi&lsquo;a bark surfaces, counting exit holes to quantify abundances of beetles (Coleoptera) within dead branches of koa, and measuring the density of arthropods within the stems of &lsquo;ākala (Rubus hawaiiensis). The diet of kiwikiu was dominated by caterpillars (Lepidoptera larvae), which comprised 90% of all prey items for 50 adult birds and 98% of all prey for two nestlings. Caterpillars were also the most important prey for Maui &lsquo;alauahio (43% for 104 adult birds) although spiders (Araneae, 16%), beetles (12%) and true bugs, planthoppers and psyllids (Hemiptera; 12%) were also important. Caterpillars were generally the most abundant type of arthropod in the foliage of koa and &lsquo;ōhi&lsquo;a, although spiders, beetles and hemipterans were also common. Total arthropod biomass and caterpillar biomass at Nakula was as great, or greater, than that observed at Hanawi and Waikamoi per unit of foliage of both koa and &lsquo;ōhi&lsquo;a. Spiders generally dominated the bark fauna on both koa and &lsquo;ōhi&lsquo;a at all sites although isopods (Isopoda), millipedes (Myriapoda: Millipeda) and lacewings (Neuroptera) were also abundant at Waikamoi and Hanawi. Total arthropod biomass on bark, as well as the biomass of several individual taxa, was significantly lower at Nakula than the other sites. Our measurement of the density of beetle exit holes in dead koa branches found no difference between Nakula and Waikamoi. Finally, no difference existed in the abundance of arthropods (primarily caterpillars and moth pupae) within &lsquo;ākala stems among sites. With the exception of bark surfaces, our results suggest that the arthropod prey base for birds on primary foraging substrates at Nakula is similar to that found at two sites within the current range of kiwikiu and Maui &lsquo;alauahio. However, our results should be viewed with caution because they are limited to the scale of individual branch, tree, or &lsquo;ākala stem. To complete the assessment, our results should be scaled up to the landscape level by determining the density of each substrate within each site. Key arthropod prey of kiwikiu and Maui &lsquo;alauahio are available at Nakula and, as habitat restoration continues, food abundance should increase to the point at which populations of these birds can be supported.

Hawaii↗

Adaptive harvest management for the Svalbard population of pink-footed geese: 2018 progress summary

This report describes progress on development and implementation of an adaptive harvest management program for maintaining the Svalbard population of Pink-footed Geese (Anser brachyrhynchus) near their target level (60,000) by providing sustainable harvests in Norway and Denmark. Specifically, this report provides an assessment of recent monitoring information and its implications for hunting seasons in 2018. An Adaptive Harvest Management (AHM) program requires specification of four elements: (a) A set of alternative population models, which bound the uncertainty about population dynamics; (b) A set of weights describing the relative credibility of the alternative models, which are updated each year based on a comparison of model predictions and monitoring information; (c) A set of alternative harvest quotas from which to choose; and (d) An objective function, by which alternative harvest strategies are evaluated and an optimal strategy chosen. The most current set of monitoring information was used to update model weights for the 1991-2017 period. Current model weights suggest little evidence for density-dependent survival and reproduction. These results suggest that the Pink-footed Goose population may have experienced a release from density-dependent mechanisms, corresponding to the period of rapid growth in population size. There is equivocal evidence for the effect of the number of days above freezing in May in Svalbard on survival, but the evidence for an effect on reproduction has been increasing in recent years. Since the 2016 hunting season, harvest quotas are prescribed on an annual basis rather than every three years because of the potential to better meet management objectives. Based on updated model probabilities, the November 2017 population size (72,000), the proportion of the population comprised of one-year-old birds (0.076), and days above freezing in Svalbard in May 2018 (27), the optimal harvest quota for the 2018 hunting season is approximately 27,000. With the agreed upon harvest allocation of 30% Norway and 70% Denmark, the national quotas are 8,100 and 18,900, respectively, which are higher than the harvests realized in previous years. In 2017 the quota for the two countries combined was 36,000, but only a harvest of about 11,400 was realized. The decrease in harvest quota for 2018 is largely attributable to the apparent decline in population size. We also describe the ongoing development of an Integrated Population Model (IPM), which uses all available demographic data for Pink-footed Geese in a single, unified analysis. IPM estimates of harvest rates of adult geese were variable and relatively low prior to the implementation of AHM (2013), and have been relatively high since. The increase in harvest rates has been accompanied by a decline in annual survival. The ratio of young-of-the-year to older birds just prior to the hunting season has been variable over time, and since about 2005 has been highly correlated with the number of days above freezing in May in Svalbard. IPM estimates of population size suggest that abundance of Pink-footed Geese has been relatively stable, or declining slightly, in recent years. Based on the IPM estimate of population size in November 2017 of 68,800 (95% credible interval: 58,200 – 79,400), the optimal harvest quota for the 2018 hunting season is 15,000. This is lower than that derived from the set of nine discrete models because the IPM estimate of November population size is lower than the November count, and because the IPM model does not consider May temperatures in Svalbard, but rather assumes reproductive success varies randomly about the mean.

Report↗