Brood size manipulations in Great Horned Owls Bubo virginianus: are predators food limited at the peak of prey cycles?

The reproduction of raptors strongly depends on food resources. It is unclear whether predators experience superabundant food during cyclic peaks of prey populations. In order to test this hypothesis, four pairs of Great Horned Owls Bubo virginianus with two young were subjected to brood size manipulations during high densities of cyclic Snowshoe Hare Lepus americanus populations in southwestern Yukon, Canada. Broods older than 35 days were temporarily enlarged by one, and then by two, young. No effects were observed when one owlet was added, but the addition of two young resulted in significant weight losses in manipulated broods. Females with enlarged broods moved farther from their nest sites at night, presumably reflecting increased hunting effort, and also spent less time near the nest during the day. Food additions to enlarged broods returned the parental behaviour to normal. We conclude that these large predators did not experience superabundant food at this stage of the breeding season during a peak in cyclic prey.     

Hatching asynchrony and growth trade‐offs within domesticated and wild zebra finch,Taeniopygia guttata,broods

The Australian zebra finch, Taeniopygia guttata, is a widely used model organism, yet few studies have compared domesticated and wild birds with the aim of examining its relevance as an evolutionary model species. Domestic and wild broods hatch over approximately 4 and 2 days, respectively, which is important given that nestlings can fledge after as little as 12 days, although 16–18 days is common. We aimed to evaluate the extent to which the greater hatching asynchrony in domestic stock may effect reproductive success through greater variance in size hierarchies, variance in within‐brood growth rates, and partial brood mortality. Therefore, by simultaneously controlling brood sizes and experimentally manipulating hatching intervals in both domesticated and wild birds, we investigated the consequences of hatching intervals for fledging success and nestling growth patterns, as well as trade‐offs. Fledging success was similarly high in domestic and wild broods of either hatching pattern. Nonetheless, between‐brood analyses revealed that domestic nestlings had significantly higher masses, larger skeletal characters, and longer wings than their wild counterparts, although wild nestlings had comparable wing lengths at the pre‐fledging stage. Moreover, within‐brood analyses revealed only negligible differences between domestic and wild nestlings, and larger effects of hatching order and hatching pattern. Therefore, despite significant differences in the hatching intervals, and the ultimate size achieved by nestlings, the domestication process does not appear to have significantly altered nestling growth trade‐offs. The present study provides reassuring evidence that studies involving domesticated zebra finches, or other domesticated model organisms, may provide reasonable adaptive explanations in behavioural and evolutionary ecology. © 2010 The Linnean Society of London, Biological Journal of the Linnean Society, 2010, 100 , 763–773.     

Habitat selection and survival of Common Goldeneye (Bucephala clangula) broods — preliminary results

Factors affecting habitat selection and survival of individual Common Goldeneye (Bucephala clangula) broods were studied. Females were marked with radio transmitters and coloured wing tags, and their movements and that of their broods were followed to investigate the pattern of lake use.Broods frequently left hatching lakes and moved varying distances and made overland travels to reach actual brood rearing lakes. Food was more abundant and pH lower in rearing lakes compared with hatching lakes. Rearing lakes also were smaller and more isolated than hatching lakes but did not differ with respect to the structure of shore vegetation.Mortality rate varied considerably between broods. However, total distance moved and the length of overland travel was not associated with increased duckling mortality. Neither was mortality associated with the size, isolation or vegetation structure of the rearing lakes.     

Habitat Use and Survival of Preflight Wild Turkey Broods

Abstract: Wild turkey (Meleagris gallopavo) broods spend the first several days of life on the ground until poult flight capabilities are attained. This is a critical period of wild turkey life history, with poult survival ranging from 12% to 52%. We measured vegetation in plots used by Rio Grande wild turkey (M. g. intermedia) preflight broods at 4 sites in southwest Kansas and the Texas Panhandle, USA, to determine microhabitat selection for ground roosting and to determine if microhabitat was related to poult survival. Hens selected ground-roost locations with more visual obstruction from multiple observation heights than random sites. Plots surrounding ground roosts had 1) greater visual obstruction; 2) increased tree decay; 3) higher percent grass, shrub, litter, and forb cover; and 4) lower percent bare ground cover than random sites. Grass, shrubs, and downed trees appeared to provide desired cover for ground-roosting broods. Poult survival increased with age of poult, size of brood, and density of shrubs 1–2 m tall. Plots used by broods <10 days old with above average survival contained more visual obstruction and shrubs than plots used by broods 10–16 days old with above average survival, signifying a shift in habitat use by successful broods as poults attain flight abilities. Density of shrubs 1–2 m tall in brood-use areas appears to be important for poult survival to 16 days of age on southern Great Plains rangeland habitats. Ground-level vegetative cover appears to be a significant factor in preflight poult survival. Provisions of ground-level vegetative cover should be considered during wild turkey brooding periods where increased poult survival is desired.     

Lesser Scaup Nest Success and Duckling Survival on the Yukon Flats,Alaska

Abstract: Over the last 20 years scaup numbers have declined, and these declines have been greatest in the northern boreal forests of Canada and Alaska where most lesser scaup (Aythya affinis) nest. We studied nest success and duckling survival of lesser scaup over 3 field seasons, 2001–2003, on the Yukon Flats National Wildlife Refuge in northeastern Alaska, USA. Daily survival rate (DSR) of nests on our study area across all 3 years was 0.943 (n = 177 nests, 95% CI: 0.930–0.954), corresponding to a nest success of only 12.3%, considerably lower than published estimates of an average nest success as high as 57% for lesser scaup in the northern boreal forest. With Mayfield logistic regression, we investigated effects on nest survival of year, clutch initiation date, and nesting habitat type (large wetlands >10 ha, small wetlands <10 ha, and wooded creeks). Neither year nor clutch initiation date influenced nest survival; however, the odds of nest success on large wetlands was 49% lower than on wooded creeks (odds ratio = 0.512, 95% CI = 0.286, 0.918). Based on the model that used only habitat type for estimation, DSR on large wetlands was 0.931 (corresponding nest success = 7.6%), DSR on small wetlands was 0.941 (nest success = 11.1%), and DSR on wooded creeks was 0.963 (nest success = 26.2%). To estimate duckling survival, we monitored 10 broods (n = 75 ducklings) over 3 field seasons by radiotagging hens at nest hatch. Most duckling mortality (94%) occurred in the first 10 days after hatch. Average duckling survival during 1–10 days was 0.321 (95% CI: 0.122–0.772), during 11–20 days was 0.996 (95% CI: 0.891–1.040), and during 21–30 days was 0.923 (95% CI: 0.769–1.041). Three of 10 hens moved all or part of their broods overland between nesting and brood-rearing wetlands for distances of 0.3–1.6 km. Our estimates of lesser scaup nest success and duckling survival on the Yukon Flats were among the lowest ever reported for ducks nesting at northern latitudes, even though the study site was in pristine boreal forest. Estimating and comparing scaup demographic rates from different geographic areas can contribute to improved conservation. Given the scarcity of information on scaup nesting in the boreal forest, basic nesting parameters are important to those trying to model scaup population dynamics.     

Ground Roost Resource Selection for Merriam's Wild Turkeys

ABSTRACT Concealment cover is important for ground-roosting wild turkey (Meleagris gallopavo) poults immediately following hatch during the vulnerable, preflight stage. We compared concealment cover resources selected at ground roosts to those of nest sites and available resources for Merriam's turkeys (Meleagris gallopavo merriami) in the Black Hills of South Dakota, USA. Females with preflight poults selected ground roosts that were similar in structure to nest sites. Ground roosts and nests were greater in visual obstruction (unit odds ratios ≥1.19) than random sites. However, ground roosts were closer to meadow-forest edges than either nests or random sites (unit odds ratios ≤0.98). Structure at ground roosts may provide visual protection from predators, and management for shrub vegetation or woody debris along meadow-pine forest ecotones will provide cover for Merriam's turkey broods.     

The cost of incubation in relation to clutch-size in the Collared Flycatcher Ficedula albicollis

This study examines the importance of avian incubation costs as determinants of clutch-size variation by performing clutch-size and brood-size manipulations in the same population of Collared Flycatchers Ficedula albicollis during the same breeding season. In 2 5 cases when three or more clutches of the same size were completed on the same day, we moved two eggs on the day after the last egg had been laid from one randomly selected clutch (C) to another (C) and moved two other eggs from this to a third clutch (C⁺). In 20 other cases of simultaneously completed clutches of the same size, we moved two randomly selected young from one brood to a second and from that moved two other young to a third (B, B and B⁺groups). Most females were weighed the day after completion of the clutch and 1–4 days before hatching of the young, and some of them also 10–14 days after hatching of the young. We measured the daily energy expenditure of females incubating manipulated clutches of 4, 6 and 8 eggs by means of the doubly-labelled water (D₂¹⁸O) technique and also recorded their nest attendance. Hatching success of fertilized eggs was reduced in the enlarged clutches compared with control and reduced clutches. Females expired on average 3142.6 ml CO₂ and expended 78.6 kJ per day while incubating, which corresponds to a metabolic intensity of 3.3 times BMR. Daily energy expenditure increased with clutch-size due to higher costs while incubating, and not because of changed activity patterns. There were no significant differences in length of incubation, female mass or mass changes between phases for the C, C and C⁺groups. In both the C and B groups, enlarged broods produced significantly more fledged young than control broods, and those significantly more than reduced broods. Fledgling tarsus-length and mass did not differ significantly between treatments in either the C or B groups. There was no significant difference in breeding success between clutch and brood manipulations. In this season, incubation costs did not entail significant fitness losses, expressed either as fledgling production or female condition. Also, control females could have raised more young to fledging age than they did with no apparent costs.     

Sitting ducklings: Timing of hatch,nest departure,and predation risk for dabbling duck broods

For ground‐nesting waterfowl, the timing of egg hatch and duckling departure from the nest may be influenced by the risk of predation at the nest and en route to wetlands and constrained by the time required for ducklings to imprint on the hen and be physically able to leave the nest. We determined the timing of hatch, nest departure, and predation on dabbling duck broods using small video cameras placed at the nests of mallard (Anas platyrhynchos; n = 26), gadwall (Mareca strepera; n = 24), and cinnamon teal (Anas cyanoptera; n = 5). Mallard eggs began to hatch throughout the day and night, whereas gadwall eggs generally started to hatch during daylight hours (mean 7.5 hr after dawn). Among all species, duckling departure from the nest occurred during daylight (98%), and 53% of hens typically left the nest with their broods 1–4 hr after dawn. For mallard and gadwall, we identified three strategies for the timing of nest departure: (a) 9% of broods left the nest the same day that eggs began to hatch (6–12 hr later), (b) 81% of broods left the nest the day after eggs began to hatch, and (c) 10% of broods waited 2 days to depart the nest after eggs began to hatch, leaving the nest just after the second dawn (27–42 hr later). Overall, eggs were depredated at 10% of nests with cameras in the 2 days prior to hatch and ducklings were depredated at 15% of nests with cameras before leaving the nest. Our results suggest that broods prefer to depart the nest early in the morning, which may best balance developmental constraints with predation risk both at the nest and en route to wetlands.     

Mid-contract management of Conservation Reserve Program grasslands provides benefits for ring-necked pheasant nest and brood survival

Conservation Reserve Program (CRP) fields may provide good habitat for nesting and brood-rearing ring-necked pheasants (Phasianus colchicus) during early stages of succession. But, the success of hens in early successional CRP, relative to late successional CRP and other grassland habitats, has yet to be evaluated. The reproductive period is especially critical for populations of pheasants, and CRP's benefits to hens and chicks may decrease as fields age because of loss of vegetative diversity, decrease in vegetation density, and accumulation of residual litter. During 2005–2006, we evaluated spatial and temporal variation in nest and brood survival for radio-marked hen pheasants in areas of northeastern Nebraska where portions of CRP fields had been recently disced and interseeded (DICRP) with legumes. Nests in DICRP tended to have a higher daily survival rate (0.984; 95% CI: 0.957–0.994) than nests in grasslands (including CRP) that were unmanaged (0.951; 95% CI: 0.941–0.972). The probability of 23-day nest success was 0.696 (95% CI: 0.631–0.762) for DICRP and 0.314 (95% CI: 0.240–0.389) for unmanaged grasslands. Daily brood survival rates varied by habitat type, brood age, and date of hatch. The probability of a brood surviving to day 21 was 0.710 (95% CI: 0.610–0.856). Brood survival rates increased with time spent in DICRP and as the brood aged. Survival decreased as broods spent more time in cropland and peaked seasonally with broods that hatched on 15 June. Brood survival probability, to 21 days, would be reduced to 0.36 (95% CI: 0.100–0.701) if broods in our sample had not used DICRP. We combined nest and brood survival in a productivity model that suggested 2,000 hens, in a landscape with no DICRP, would produce 1,826 chicks, whereas the same hens in a landscape of 100% DICRP would produce 5,398 chicks. Production of first-year roosters more than doubled when hens nested in DICRP. Without DICRP, population growth rates of pheasant populations usually declined; with DICRP, populations stabilized with at annual survival rates of 0.3 or greater. The positive response of nest and brood survival to discing and interseeding CRP provides further evidence that CRP fields must be managed to optimize wildlife benefits. © 2012 The Wildlife Society.     

Survival of Dusky Canada Goose Goslings in Relation to Weather and Annual Nest Success

Abstract The dusky Canada goose (Branta canadensis occidentalis) population has been in long-term decline, likely due to reduced breeding productivity, but gosling survival of this population had not been examined. We studied gosling survival in broods of radiomarked adult females on the western Copper River Delta, Alaska, USA, during 1997–1999 and 2001–2003. Survival estimates for dusky Canada goose goslings to 45 days (x̄ = 0.32) were below estimates from most previous studies of geese. Daily survival of goslings increased with age and decreased with date of hatch. Precipitation during the first 3 days post-hatch was negatively related to gosling survival and this effect increased with date. Annual estimates of gosling survival were positively correlated with annual estimates of nest success, suggesting overlap in factors affecting nest and gosling survival. Nest success probably also directly affected gosling survival, because survival decreased with hatch date and more broods hatched from renests during years with low nest success. Gosling survival appears to play an important role in limiting current productivity of this population. Management directed at increasing nest success would likely also improve gosling survival. We recommend additional research directed at examining sources of gosling mortality and the link between nest success and gosling survival.     

An experimental approach to the brood reduction hypothesis in Magellanic penguins

In many bird species, eggs in a brood hatch within days of each other, leading to a size asymmetry detrimental to younger siblings. Hatching asynchrony is often thought of as an adaptive strategy, and the most widely studied hypothesis in relation to this is the ‘brood reduction hypothesis’. This hypothesis states that when food resources are unpredictable, hatching asynchrony will allow the adjustment of the brood size maximizing fledging success and benefitting parents. The Magellanic penguin Spheniscus magellanicus is an appropriate species to test this hypothesis because it has a 2‐egg clutch that hatches over a 2‐d interval with a broad range of variation (–1 to 4 d), it shows facultative brood reduction, and food abundance between breeding seasons is variable. We performed a manipulative study at Isla Quiroga, Argentina, during three breeding seasons (2010–2012) by forcing broods to hatch synchronously (0 d) or asynchronously (2 or 4 d). Years were categorized based on estimated food abundance. Our study provided mixed results because in the low estimated food abundance year asynchronous broods did not have higher nestling survival than synchronous broods, and the second‐hatchling in asynchronous broods did not die more often than those in synchronous broods. On the other hand, younger siblings of 4‐d asynchronous broods starved earlier than those of synchronous broods, and 2‐d asynchronous broods fledged heavier young than synchronous broods. Asynchronous hatching would seem to benefit reproduction in this species, not with respect to survival, but in terms of the advantages it can accord to nestlings and, in terms of lower costs, for parents raising nestlings.     

Survival of Greater Sage‐Grouse broods: survey method affects disturbance and age‐specific detection probability

Investigators rely on brood surveys to estimate annual fecundity of game birds. However, investigators often do not account for factors that influence brood detection probability nor rarely document how much females and their broods are disturbed (flush rates) during surveys, which could lead to biased survival estimates. We used 45 radio‐tagged female Greater Sage‐Grouse (Centrocercus urophasianus) with broods to compare detection probabilities and document disturbance among four survey methods to allow future investigators to select the method that best meets their objectives. These methods included daytime flush, daytime visual, nocturnal spotlight, and fecal surveys at nocturnal roost sites, with the latter being a novel method. We used Cormack–Jolly–Seber (CJS) models to compare detection probability and daily survival estimates for visual and fecal surveys of broods 0–47 d post‐hatch and a double‐survey approach to compare detection probabilities among flush, fecal, and spotlight surveys ~42 d post‐hatch when investigators often determine brood fate. From CJS models, detection probability for visual surveys increased with brood age (0.618–0.881), whereas detection probability for fecal surveys did not (0.748). Daily survival probability estimates increased with brood age and differed annually based on fecal surveys (2016: 0.978–1.000 and 2017: 0.839–0.998). We detected age‐specific daily survival probability with visual surveys (0.956–0.997), but not annual differences. Based on the double‐survey approach, detection probability was high (0.857–1.000) for all methods. We flushed ~310–750% fewer females and broods during fecal and spotlight surveys than during both types of daytime surveys. Our results highlight the need to account for detection probabilities among methods and document disturbance to hens and broods that can help investigators design surveys to minimize impacts to birds. Furthermore, our result suggest that actions to improve brood survival during the first week post‐hatch may improve local recruitment.     

A novel PCR‐based genetic marker shows that sex of offspring does not account for hatch‐order effects on growth,survival and dominance in Pūkeko Porphyrio melanotus melanotus

Intra‐brood competition can influence a variety of fitness‐related traits in birds. Previous research on the joint‐nesting Pūkeko Porphyrio melanotus melanotus, a New Zealand subspecies of Australasian Swamphen, showed that chicks that hatched earlier in a brood tended to grow faster, were more likely to survive and had higher dominance status as adults than later hatched nest‐mates. However, this finding could be due to changes in offspring sex ratio across hatch order (e.g. if males tend to hatch earlier), which was not previously examined because of methodological challenges associated with sexing nestling Pūkeko. Here, we report a useful PCR‐based genetic marker to determine the sex of Pūkeko. We then used new sex‐specific data to re‐examine patterns of offspring growth, survival and dominance. We found that the sex of offspring does not account for the hatching‐order patterns related to social dominance, growth or survival. Furthermore, changes in offspring sex ratio across hatching‐order were negligible and offspring sex ratios did not differ significantly between the primary female and secondary female broods (in joint‐clutch nests), or when comparing primary female and single female broods. We found no clear evidence for sex ratio bias according to hatching‐order and conclude that hatching‐order and not offspring sex explain patterns of growth, survivorship and adult dominance in Pūkeko.     

Growth and survival of neotropic cormorant (Phalacrocorax brasilianus) chicks in relation to hatching order and brood size

We investigated chick development and feeding rate in the neotropic cormorant, Phalacrocorax brasilianus, in a colony in Central Chile. The year of our study was characterized by relatively good foraging conditions. Brood sizes varied from two to five chicks, and hatching was asynchronous, with gaps of 0 to 6 days between the youngest and the oldest chick. Egg size declined over laying order in three-egg clutches, but not in four-egg clutches. Hatch weight did not vary with hatching position, irrespective of brood size. Chicks increased mass on average by 60 g/day between 8 and 20 days of age. Growth rates and survival to fledging depended on hatching position only in broods of four, where D-chicks grew slower and showed a higher pre-fledging mortality. There was a non-significant tendency that also A-, B-, and C-chicks in broods of four grew slower than in smaller broods. Average number of fledglings was 2.76. Feeding frequency decreased with chick age between the ages of 10–40 days. Four-chick broods received more feeds per day than smaller broods, leading to a similar per-chick feeding frequency across all brood sizes. D-chicks were clearly disadvantaged in growth and survival, and facultative brood reduction occurred.     

Wild Turkey Nest Success in Pine-Dominated Forests of the Southeastern United States

Nest success is a primary component of productivity for wild turkeys (Meleagris gallopavo; turkeys) and there is concern that turkey productivity is declining across the southeastern United States. We evaluated the influence of nest site and landscape characteristics on risk of nest failure for turkeys in pine (Pinus spp.)-dominated forests across the southeastern United States. We used Cox proportional hazard models to evaluate daily hazard of nest failure associated with nest site and landscape metrics within 500-m and 1-km buffers centered on nests. Of 451 nests monitored (n = 320 females) between 2014 and 2018, 76% failed, with predation as the primary cause. Daily hazard of nest failure increased by 1.2% for each day that females delayed nest incubation following the mean nesting date (29 Apr; β_day = 0.010 ± 0.002 [SE]; hazard ratio [HR] = 1.01, 95% CI = 1.006–1.015). Environmental covariates associated with risk of nest failure included the maximum enhanced vegetation index (EVI) and distance to the nearest ecotone. Daily hazard increased with increasing distance away from an ecotone (β_ecotone = 0.16 ± 0.06; HR = 1.17, CI = 1.03–1.32) and with lower EVI around the nest (β_EVI = −0.30 ± 0.06; HR = 0.74, CI = 0.65–0.83). Additional nest site or landscape covariates were included in competitive models but did not influence risk of nest failure significantly. Our study highlights the importance of considering landscape context when designing and implementing land management actions intended to enhance wild turkey reproduction. Our findings suggest that landscape metrics thought to be important to turkeys in northern agro-forested landscapes may not be relevant to turkeys in pine ecosystems of the southeastern United States. © 2021 The Wildlife Society.     

The survival of gamebird (Galliformes) chicks in relation to pesticide use on cereals

Field experiments were carried out to test the effects of cereal pesticides (herbicides, fungicides and insecticides) on chick survival of Grey Partridge Perdix perdix , Red-legged Partridge Alectoris rufa and Pheasant Phasianus colchicus. On fields in experimental plots the outer 6 m of cereal (the headland) were not sprayed with pesticides from 1 January 1984, whereas control plots were fully sprayed. Gamebird brood counts were carried out after the cereal harvest. In addition, nine Grey Partridge broods were radio-tracked for 21 days after hatching (four in sprayed plots and five in unsprayed plots) to determine their movements, home range size and survival in relation to pesticide spraying.
The mean brood size of Grey Partridge and Pheasant was significantly higher on plots where field edges were unsprayed than on fully sprayed control plots. Data for Red-legged Partridge were inconclusive. The survival of individually marked Grey Partridge broods was negatively related to the distance moved between successive nocturnal roost sites. Survival was significantly higher, the distance moved between roost sites significantly shorter and the proportion of home range including headland significantly greater for broods feeding in spring barley fields with unsprayed field edges compared with broods feeding in fully sprayed fields.     

Sex ratio and fledging success of supplementary-fed Tengmalm's owl broods

A nest box population of Tengmalm's owls (Aegolius funereus) in northern Sweden was studied to investigate the effects of extra food on the sex ratio between hatching and fledging in this sexually size-dimorphic species. The brood size and brood sex ratio of supplementary-fed and control broods were compared. Newly hatched nestlings were blood sampled and sexed by polymerase chain reaction (PCR) amplification of the sex-linked CHD1Z and CHD1W genes. The brood sex ratio at hatching was strongly male biased (65%); this was also the case in broods where all eggs hatched (72%). There was no relationship between hatch order and sex ratio, and hatching sex ratio did not vary significantly with laying date. Brood size decreased between hatching and fledging, but did not differ between fed and control broods at either stage. Brood sex ratio did not differ between hatching and fledging, and fledging sex ratio did not differ between fed and control broods. It was concluded that, at least during the year in which the study was carried out, feeding had no effect on brood reduction, and that male and female nestlings did not show any differential mortality. The mechanisms behind the male-biased sex ratio at hatching, and any possible adaptive reasons for it, are not known.     

Robust assessment of associations between weather and eastern wild turkey nest success

Temperature and precipitation have been identified as factors that potentially influence eastern wild turkey (Meleagris gallopavo silvestris) reproduction, but robust analyses testing the relationship between weather parameters and turkey nest success are lacking. Therefore, we assessed how weather influenced turkey daily nest survival using 8 years of data collected from 715 nests across the southeastern United States. We also conducted exploratory analyses investigating if weather conditions during or prior to nesting best predicted nest success. We then assessed the possible implications of climate change through 2041–2060 for future eastern wild turkey daily nest survival and nest success for variables determined significant in analyses. During incubation, positive anomalies of minimum daily temperature were associated with greater daily nest survival. Precipitation during nesting was not a good predictor of daily nest survival. Exploratory analyses unexpectedly indicated that weather conditions in January prior to incubation were more important to nest success than weather conditions during incubation. In January, negative anomalies of minimum temperature and greater average daily precipitation were associated with greater nest success. Projections of future nest success or daily nest survival based on these relationships with the predictive covariates, and informed by climate models, suggest that nest success may increase as January precipitation increases and that daily nest survival may increase as temperature during incubation increases. These positive associations could be offset by a negative association between nest success and the expected increases in January minimum average temperature. Additional research is needed to investigate causes of these relationships and assess the implications of climate change for eastern wild turkey poult survival.     

Greater Sage-Grouse Response to the Physical Footprint of Energy Development

Energy infrastructure and associated habitat loss can lead to reduced reproductive rates for a variety of species including the greater sage-grouse (Centrocercus urophasianus). Our goal was to refine our understanding of how the physical footprint of energy development relates to sage-grouse nest and brood survival. Our survival analyses were conditional upon the amount of surface disturbance female sage-grouse were exposed to during reproductive stages. We quantified levels of exposure and compared them to the surface disturbance levels of the surrounding area. From 2008–2014, we collected data in 6 study areas in Wyoming, USA, containing 4 primary types of renewable and nonrenewable energy development. Our research focused on press disturbance (i.e., disturbance sustained after initial disturbance and associated with existing energy infrastructure and human activity). Our results suggest exposure to press disturbance during nesting and brood-rearing was related to lower nest and brood survival, which manifested at different spatial scales. Our analysis of nest survival suggested that the likelihood of a successful nest was negatively associated with the amount of press disturbance within an 8-km² area. Broods exposed to any press disturbance within a 1-km² area were less likely to survive compared to broods not exposed to press disturbance. Female sage-grouse consistently used habitat with lower disturbance levels during reproductive periods. Greater than 90% of nest and brood-rearing locations were in habitat with <3% press disturbance within a 2.7-km² area. Our research links surface disturbance associated with press disturbance to reproductive costs incurred by sage-grouse exposed to diverse energy development. Our results demonstrate a pattern of female avoidance of areas where press disturbance was high during nesting and brood-rearing and survival of nests and broods were highest in areas that had the least amount of disturbance. Our findings underscore the importance of minimizing disturbance to maintain viable sage-grouse populations. © 2020 The Wildlife Society.     

Within-season sequential density dependence regulates breeding success in mallards Anas platyrhynchos

Density dependence in vital rates is a key issue in population ecology but remains largely unexplored experimentally. We studied breeding success, lake use, and prey availability in wild mallards Anas platyrhynchos on small nemoral lakes in a replicated, two-year cross-over experiment in which pair density was increased. The number of wild mallards that settled on lakes prior to introductions of extra pairs did not differ between control and introduction years. Introductions led to a lake-level reduction in the number of broods observed. However, the number of stage 2+ (almost fledged) ducklings did not differ between treatments, nor did lake utilization by nonbreeding adults, broods and ducklings. Prey resource availability differed greatly among lakes, but it did not correlate with breeding success. Partialling out the possible effect of food competition from wild adult nonbreeding mallards did not change this conclusion. Our study demonstrates sequential density dependence in breeding success; introductions caused a decrease in brood number, but despite fewer broods a similar number of nearly fledged ducklings were produced. We suggest that predation and/or lake change of broods soon after hatching created these patterns. We conclude that using a single and late measure of breeding success such as fledged birds can mask regulatory processes. Implications of density dependence and its relation to individual reproductive success are understood better if breeding success is decomposed into nest success, duckling survival and fledgling survival.