REPRODUCTION BY NORTHERN BOBWHITES IN WESTERN OKLAHOMA

Abstract: We studied northern bobwhites (Colinus virginianus) in western Oklahoma, USA, during the nesting seasons of 1992–2001. We obtained latitude-specific information on nesting biology and tested hypotheses on the cause of declines in clutch size with progression of the nesting season and on the phenological relation of first, second, and third nesting attempts. For pooled data on bobwhites alive during 15 April-15 September, 64 ± 6.5% of juvenile females (n = 56), 90 ± 10.0% of adult females (n = 9), 13 ± 4.1% of juveniles males (n = 68), and 41 ± 10.7% of adult males (n = 22) incubated ≥ 1 nest. Bobwhites that entered the reproduction period starting on 15 April (n = 229) accumulated 203 nesting attempts (male and female incubations), which translated to 1.7 attempts/hen for all hens that entered (n = 117) and 3.1 attempts/hen for hens that survived to 15 September (n = 65). Overall success for incubated nests (48 ± 2.8%, n = 331) was independent of sex-age class and nesting attempt (1, 2, 3), but it declined at a rate of 2.37%/year (95% CL = 1.10–3.64%/year) during the study. Clutch size declined by 1 egg for every 14–20 elapsed days in the nesting season and the rate of decline was independent of incubation attempt (1 or 2); this result suggests that lower clutch sizes later in the nest season were not necessarily a function of re-nesting. Ending of nest-incubation attempts (1, 2, 3) occurred within an 8-day period from 26 August-2 September. Our results implied that early-season nesting cover is a management concern and that high nest success is possible in the absence of nest predator suppression where abundant nest sites occur across the landscape.     

Habitat-Suitability Bounds for Nesting Cover of Northern Bobwhites on Semiarid Rangelands

ABSTRACT Northern bobwhite (Colinus virginianus) is a species for which extensive knowledge exists regarding its ecology, life history, and habitat. Although the qualitative aspects of bobwhite habitat have been described and known for many decades, researchers have neglected to characterize bobwhite habitat quantitatively (i.e., habitat selection). Thus, biologists have been capable of identifying components that compose bobwhite habitat but have only been able to speculate on how much of each component was necessary. We documented selection-avoidance behavior of nesting bobwhites in Brooks County, Texas, USA, during May-August, 2004–2005. We measured 5 vegetation features (i.e., nesting-substrate ht and width, suitable nest clump density, herbaceous canopy coverage, and radius of complete visual obstruction) at nest sites (n = 105) and at random points (n = 204). We used continuous selection functions to assess habitat use and identify bounds of suitability. Selection domains for nesting-substrate height and radius of complete visual obstruction were 16.9–31.2 cm and 1.05-4.35 m, respectively. Across all measurements, bobwhites selected for nest sites with a nesting-substrate width ≥22.4 cm, suitable nest-clump density ≥730 nest clumps/ha, and herbaceous canopy coverage ≥36.7%. This knowledge will provide an important foundation for managers to evaluate current nesting conditions on semiarid rangelands and provide a basis for habitat management aimed at creating suitable nesting habitat for bobwhites.     

Demographic Sensitivity of Population Change in Northern Bobwhite

Abstract: The northern bobwhite (Colinus virginianus) is an economically important gamebird that is currently undergoing widespread population declines. Despite considerable research on the population ecology of bobwhites, there have been few attempts to model population dynamics of bobwhites to determine the contributions of different demographic parameters to variance of the finite rate of population change (Λ). We conducted a literature review and compiled 405 estimates of 9 demographic parameters from 49 field studies of bobwhites. To identify demographic parameters that might be important for management, we used life-stage simulation analyses (LSA) to examine sensitivity of Λ to simulated variation in 9 demographic parameters for female bobwhites. In a baseline LSA based on uniform distributions bounded by the range of estimates for each demographic parameter, bobwhite populations were predicted to decline (Λ = 0.56) and winter survival of adults made the greatest contribution to variance of Λ (r² = 0.453), followed by summer survival of adults (r² = 0.163), and survival of chicks (r² = 0.120). Population change was not sensitive to total clutch laid, nest survival, egg hatchability, or 3 parameters associated with the number of nesting attempts (r²<0.06). Our conclusions were robust to alternative simulation scenarios, and parameter rankings changed only if we adjusted the lower bounds of winter survival upwards. Bobwhite populations were not viable with survival rates reported from most field studies. Survival rates may be depressed below sustainable levels by environmental conditions or possibly by impacts of capture and telemetry methods. Overall, our simulation results indicate that management practices that improve seasonal survival rates will have the greatest potential benefit for recovery of declining populations of bobwhites.     

Impacts of introduced grasses on breeding season habitat use by northern bobwhite in the South Texas plains

Introduced grasses may affect diversity of native fauna and flora adversely, and disrupt ecosystem processes. Many rangelands in South Texas have been seeded to or have been colonized by buffelgrass (Pennisetum ciliare) and Lehmann lovegrass (Eragrostis lehmanniana), perennial bunchgrasses native to Africa. The objective of this research was to quantify impacts that these 2 species of introduced grasses may have on northern bobwhite (Colinus virginianus) habitat use on South Texas rangelands during the breeding period (Apr–Aug). We evaluated the effects of buffelgrass and Lehmann lovegrass on northern bobwhite nest habitat (n = 35 nests) and general habitat use sites (n = 86 radiomarked quail) with logistic regression and habitat selection functions based on simple saddlepoint approximations. Buffelgrass was used as a nesting substrate at 11% of nests; however, vegetation height and visual obstruction between 1 cm and 30 cm were the best predictors of nest site use. Areas of introduced grass coverage ≥15–20% were avoided by northern bobwhites at general habitat use organism-centered points, but not at nest site use points. Introduced grass coverage and forb coverage were the best predictors of general habitat use, and bobwhites avoided areas with ≥18% introduced grass cover. These results suggest that avoidance of areas with extensive introduced grass cover may indicate a reduction in usable habitat space for northern bobwhite in the western South Texas plains. Maintaining native grass stands while implementing localized control of introduced grasses could be used as a strategy to promote habitat for northern bobwhites. © 2011 The Wildlife Society.     

Nest success of northern bobwhite on managed and unmanaged landscapes in southeast Iowa

Range-wide declines in northern bobwhite populations (Colinus virginianus) have been attributed to concomitant loss of breeding habitat. Bobwhite management efforts to restore this habitat resource can be informed by empirical studies of associations between breeding success and multi-scale habitat attributes. We compared bobwhite nest success in 2 southern Iowa landscapes as a function of microhabitat and landscape composition. Lake Sugema Fish and Wildlife Area (LSWA) was managed to promote bobwhite recruitment, and Harrisburg Township (HT) was an adjacent landscape dominated by private agricultural production. Survival rate modeling based on telemetry data provided evidence for age-specific daily nest survival rate. Daily survival rates decreased as nest age increased, but the decline was more severe at HT. Nest survival at LSWA (S = 0.495, SE = 0.103) was nearly twice that on HT (S = 0.277, SE = 0.072). We found no evidence that habitat composition or spatial attributes within 210 m of a nest site significantly influenced nest success. Forb canopy at the nest site had a positive influence on nest success at HT but not at LSWA. We suggest nesting habitat with greater forb canopy cover will increase the opportunity for nesting success in landscapes with limited nesting habitat. © 2010 The Wildlife Society.     

Identifying Predators and Nest Fates of Bobwhites in Southern Texas

Abstract: Predation is the primary cause of nest failure for northern bobwhites (Colinus virginianus). There are few reliable data documenting the species diversity and relative importance of bobwhite nest predators in southern Texas, USA. We used infrared video-monitoring systems to document nest fates of 127 bobwhite nests over 4 nesting seasons from 2002 to 2005 in southern Texas. A majority of depredation events (83%) were caused by 4 species: coyote (Canis latrans), striped skunk (Mephitis mephitis), southern fire ant (Solenopsis xyloni), and badger (Taxidea taxus). Observed bobwhite nest fates for the study period were 0.50 successful, 0.34 depredated, and 0.16 abandoned or undetermined. A universal approach to mitigating nest predation is not likely to be applicable in regions similar to southern Texas, with high nest-predator diversity (e.g., fire ants, rodents, and mammalian carnivores). We believe that infrared video surveillance is a valuable tool for documenting baseline information on predator context and nest fate for many avian species, considering the limitations of past methods (e.g., postfate evidence).     

IDENTIFYING PREDATORS AT NORTHERN BOBWHITE NESTS

Abstract: We identified nest predators of northern bobwhites (Colinus virginianus) on private lands in northern Florida and southern Georgia, USA, using continuous infrared micro-video cameras, 1999–2001, and compared these results to predictions based on diagnostic sign at nests. Mammals (59%), snakes (29%), and ants (12%) accounted for known bobwhite nest depredations. Mammalian predators, in order of importance, were the raccoon (Procyon lotor), nine-banded armadillo (Dasypus novemcinctus), Virginia opossum (Didelphis virginiana), bobcat (Lynx rufus), hispid cotton rat (Sigmodon hispidus), and coyote (Canis latrans). Using diagnostic sign, technicians correctly classified 30% of mammalian depredations to species and overestimated nest depredations by snakes. A classification tree model correctly classified 75% of the test sample (n = 33) into “mammal” or “snake” categories, but still overestimated depredations by snakes. We documented a broader predator community upon bobwhite eggs than previously known for northern Florida and southern Georgia and confirmed that snakes were significant nest predators in some years. We conclude that diagnostic sign at depredated nests was unreliable for identifying nest predators of northern bobwhites.     

Simulating northern bobwhite population responses to nest predation,nesting habitat,and weather in south Texas

Nest predation is thought to be one of the major factors limiting northern bobwhite (Colinus virginianus) populations. We examined the relative impact of altering nest-predation rate, nesting habitat, and weather (i.e., temp and precipitation) on northern bobwhite population dynamics in a hypothetical 15,000-ha subtropical-rangeland ecosystem in south Texas using a simulation model. The systems model consisted of a 3-stage (i.e., eggs, juv, and ad) bobwhite population with dynamics influenced by variables affecting production, recruitment, nest predation, and mortality. We based model parameters on data collected from a 3-yr nest-predator study employing infrared-camera technology, from ongoing field research using a radio-marked population of wild bobwhites, and from the literature. The baseline simulated bobwhite population dynamics corresponded closely to empirical data, with no difference between medians of simulated (n = 30 yr) and observed bobwhite age ratios over a 28-yr period. Similarly, a time-series comparison of simulated and observed age ratios showed most (89%) observed values fell within the 5th and 95th percentiles of the simulated data over the 28-yr period. We created simulated population scenarios representing 1) baseline historical conditions, 2) predator control, 3) low precipitation, 4) low precipitation with predator control, 5) high temperature, 6) high temperature with predator control, 7) reduced nest-clump availability, and 8) reduced nest-clump availability with predator control that resulted in considerably different median bobwhite densities over 10 yr. For example, under simulated predator control, populations increased by about 55% from the baseline scenario, whereas under simulated reduced nest-clump availability, populations decreased by about 75% from the baseline scenario. Comparisons of time-series for each scenario showed that reduced nest-clump availability, low precipitation, and high temperature reduced bobwhite densities to a larger degree compared to a natural nest predation rate. Reduced nest-clump availability resulted in the most substantial decline of simulated bobwhite densities. Simulations suggested that management efforts should focus on maintaining adequate nest-clump availability and then possibly consider nest predator control as a secondary priority. © 2010 The Wildlife Society     

Nesting ecology of a naturalized population of Mallards Anas platyrhynchos in New Zealand

Investigating the reproductive ecology of naturalized species provides insights into the role of the source population's characteristics vs. post‐release adaptation that influence the success of introduction programmes. Introduced and naturalized Mallards Anas platyrhynchos are widely established in New Zealand (NZ), but little is known regarding their reproductive ecology. We evaluated the nesting ecology of female Mallards at two study sites in NZ (Southland and Waikato) in 2014–15. We radiotagged 241 pre‐breeding females with abdominal‐implant transmitters and measured breeding incidence, nesting chronology and re‐nesting propensity. We monitored 271 nests to evaluate nest survival, clutch and egg size, egg hatchability and partial clutch depredation. Breeding incidence averaged (mean ± se) 0.91 ± 0.03, clutch size averaged 9.9 ± 0.1 eggs, 94 ± 2% of eggs hatched in successful nests, partial depredation affected 6 ± 1% of eggs in clutches that were not fully destroyed by predators, and re‐nesting propensity following failure of nests or broods was 0.50 ± 0.003. Nesting season (first nest initiated to last nest hatched) lasted 4.5 months and mean initiation date of first detected nest attempts was 28 August ± 3.3 days. Smaller females were less likely to nest, but older, larger or better condition females nested earlier, re‐nested more often and laid larger clutches than did younger, smaller or poorer condition females. Younger females in Southland had higher nest survival; cumulative nest survival ranged from 0.25 ± 0.007 for adult females in Waikato to 0.50 ± 0.007 for yearling females in Southland. Compared with Mallards in their native range, the nesting season in NZ was longer, clutches and eggs were larger, and nest survival was generally greater. Different predators and climate, introgression with native heterospecifics and/or the sedentary nature of Mallards in NZ may have contributed to these differences.     

吉林白城地区草原栗斑腹(巫鸟)窝卵数、营巢成功率和繁殖成功率的研究

对分布于吉林白城地区草原生境中栗斑腹巫鸟的窝卵数、营巢成功率和繁殖成功率的初步研究结果表明 ,繁殖期栗斑腹巫鸟种群的平均窝卵数为 5 .0 9± 0 .5 8枚 /巢 ;窝卵数与产卵期、出巢数与产卵期、窝卵数与卵大小之间呈负相关 ,产卵期与孵化率之间存在极显著的负相关关系 ,巢外径与窝卵数之间存在显著的正相关关系 ,巢的其余指标均与窝卵数呈正相关 ;平均孵化期为 12± 0 .4 9d ,孵化率为 36 .3% ,繁殖成功率为 11.11% ;7日龄以上的雏鸟群体大小为 2 .5 6± 1.5 3只 ,栗斑腹巫鸟的雏鸟存活率为 2 7.6 9% .     

Distribution and breeding ecology of the Ferruginous Duck Aythya nyroca in Algeria

We conducted a survey of the distribution of Ferruginous Duck Aythya nyroca across Algeria and analysed the influence of nest-site characteristics on nesting success at a Ramsar site, Lake Tonga. The species was found to occupy different wetlands (freshwater lakes, brackish marshes and salt lakes) across three major climatic belts (subhumid coastal strip, semi-arid Hauts Plateaux and arid Sahara). Mean clutch size of successful nests was 13.3 ± 6.0 eggs (N = 26) with a hatching rate of 74% for successful clutches. Nesting success was recorded for 44% of nests with clutch desertion (72.7%) accounting for the majority of failed clutches. Egg size of the study population, which breeds at the southern limit of the species’ range, was significantly smaller than that of its northerly counterparts. Clutch size was negatively related to egg size and positively associated with depth of water below the nest, suggesting that older, more experienced or high-quality birds monopolised the safest sites. Successful clutches were significantly associated with tall vegetation, suggesting that when nesting is carried out mainly on offshore floating islets, protection against aerial predators and heat stress determine nesting outcome. Conspecific brood parasitism was significantly and positively associated with deferred egg-laying and smaller egg size, suggesting an age-dependent mechanism.     

Effects of clutch sizes and incubation stage on nest desertion in the female Common Eider Somateria mollissima nesting in the high Arctic

In bird species, one of the trade-offs between reproduction and survival appears in the parental decision to desert the nest. Nest desertion is modulated by several factors including clutch size. However, the incubation stage at which predation occurs is also an important factor. In this study, we examined whether nest desertion was linked to initial clutch size, partial clutch predation (final clutch size) and the incubation stage at which it happened in a capital breeder: the female common eider (Somateria mollissima) nesting in the high Arctic. The study was performed in Kongsfjorden in 2002 on the western coast of the Svalbard Archipelago (78°55′N, 20°07′E). We observed that nest desertion was higher when the initial clutch size was small. Also, females deserted their nests more during the first third of incubation than later. Thus, as incubation proceeded, nest desertion was less likely to occur even after egg reduction. Our results pointed out that this parental decision in female eiders seemed to depend on initial clutch size and on the date into incubation of clutch reduction. Sophie Bourgeon and Francois Criscuolo contributed equally to the work     

Factors influencing reproductive performance of northern bobwhite in South Florida

Reproductive success is a critical component of individual fitness, and also an important determinant of growth rates of populations characterized by early maturity and high fecundity. We used radiotelemetry data collected during 2003–2008 to estimate reproductive parameters in a declining northern bobwhite (Colinus virginianus) population in South Florida, and to test hypotheses regarding factors influencing these parameters. The overall clutch size was 12.10 ± 0.22, but females laid more eggs in their first clutch (12.43 ± 0.24) than in subsequent clutches (10.19 ± 0.53) within a nesting season. Daily nest survival was higher for first (0.966 ± 0.003) than subsequent nests (0.936 ± 0.011). Hatchability (proportion of laid eggs that hatched conditional upon nest survival to hatching) was 0.853 ± 0.008, but was higher for nests incubated by females (0.873 ± 0.009) than those incubated by males (0.798 ± 0.018). The proportion of individuals attempting a second nest was 0.112 ± 0.024 and 0.281 ± 0.040 when the first nest was successful and failed, respectively. Hatchability was lower when the nesting habitat was burned the previous winter. We found no evidence that food strip density (a management practice to provide supplemental food) influenced any of the reproductive parameters. Mean summer temperature affected hatchability, nest survival, and proportion of nests incubated by males. Overall, the reproductive output in our study population was lower than that reported for most other bobwhite populations, indicating that low reproductive performance may have contributed to bobwhite population declines in our study site. These results suggest that current management practices, particularly those related to habitat and harvest management, need careful evaluation.     

Interactive effects of time and vegetation on reproduction of redshanks (Tringa totanus) breeding in Wadden Sea salt marshes

As shown for various species, nesting waders are non-randomly distributed on wetlands and preferentially select riparian nest-sites adjacent to limnic or marine waterbodies. Studying the redshank Tringa totanus, we tested the hypotheses that, in a coastal wader species which conceals its clutch in vegetation, predation and hatching success are affected by vegetation zonation, and that breeding in lower salt marsh areas has negative consequences for reproduction. We further predicted effects of timing of breeding and breeding experience/age of adults potentially reflected by egg biometrics both on nest-site selection and reproduction. Effects of vegetation, space, time and individual quality on hatching success of redshanks were studied in the German part of the Wadden Sea. Dominant plant species, vertical vegetation structure and nest concealment varied significantly between nests. Variation in nest concealment was relatively low: about 90% of clutches were classified as being well concealed. This variation was explainable by vegetation structure but not by vegetation composition at the nest-site, distance to shoreline, and time of clutch initiation. Vertical vegetation structure varied by dominant plant species but not by distance to shoreline and time of clutch initiation. Hatching success of clutches was low (10.6%) due to high predation (daily predation rate: 7.4%). Hatching success and duration of clutch survival were negatively and predation positively related to the date of clutch initiation. Furthermore, negative relationships were found between egg size and predation and duration of survival, respectively. We assume that concealed nests, early breeding and breeding experience diminish predation in salt marsh breeding redshanks. Thus, redshank reproduction appears to be affected by interactive effects of timing of breeding and vegetation facilitating early breeding. In contrast to open-nesting species, breeding in riparian habitats next to waterbodies may be disadvantageous for species breeding concealed in vegetation if these are covered by less structured vegetation.     

Breeding success and chronology of Wood Storks Mycteria americana in northern and central Florida, U.S.A.

The breeding success and chronology of Wood Storks Mycteria americana were studied at eight colonies in northern and central Florida during 1981–1985. Mean ± s.d. clutch size for all colony-years was 3.07 ± 0.56 (n = 2694 nests), with three-egg clutches (72%) most frequent. Mean clutch size among all colonies and years ranged from 2.73 ± 0.55 to 3.41 ± 0.61. Many colonies exhibited significant negative trends in clutch size with, hatching date because of a proportional decrease in four-egg clutches later in the season. Mean colony clutch size was not correlated with nest numbers, nesting density or mean hatching date within most years. Mean ± s.d. number of fledglings for all colonies and years was 1.29 ± 1.16 fledglings per nest (n = 2812 nests). Mean annual fledging rates in colonies ranged from 0 (colony failed) to 2.66 fledglings per nest. Most breeding failure occurred prior to egg hatching, and the second highest mortality occurred between hatching and 2 weeks of age. Four-egg clutches fledged more storks than three-egg clutches, which in turn were more successful than two-egg clutches. However, all clutch sizes showed similar fledgling per egg rates. The seasonal decline in productivity was associated proportionally with smaller clutch sizes later in the breeding season. An increase in mean hatching date was correlated with an increase in latitude. There was greater within-year breeding synchrony among colonies than interyear breeding synchrony within each colony. Breeding synchrony was not correlated with mean hatching date, latitude, longitude, nest numbers or nesting density.     

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.     

Age and clutch size variation in Dusky Flycatcher nest survival

Examination of spatial and temporal factors that influence nest survival can provide insight into habitat selection, reproductive decisions (e.g., clutch size), population dynamics, and conservation requirements for species. We used nest survival data for the Dusky Flycatcher Empidonax oberholseri to examine several factors that may influence nesting success. Our prediction was that the number of nest initiations would be positively associated with period nest survival. We used a model selection framework and found that nesting success was a function of clutch size and a cubic effect of age. Clutches with one, two, three, and four eggs had period survival rates of 0, 0.05, 0.33, and 0.49, respectively. Daily survival rates decreased from the onset of egg-laying and increased during the later stages of incubation before remaining relatively constant through the later portions of the nestling stage. Model-selection criterion provided support for a date effect on daily survival (i.e., daily nest survival declined across the nesting season) although the 95% confidence interval for the estimate included zero. We found that the majority of nest initiations occurred early in the nest season and declined across the season as period nest survival declined. Our prediction concerning nest survival was partially supported. In addition, we found substantial positive associations between clutch size and nest survival. While low daily survival rates for clutches with one or two eggs suggested that individuals may have reduced reproductive effort in response to nest predation risk, we did not find strong evidence that individuals reduced their clutch sizes in subsequent nest attempts. Alternative predictions, including the preferential settlement of higher quality individuals (e.g., those with the ability to lay full clutches to replace depredated nests) into high-quality habitat and differences in behavior patterns (e.g., number of visits to provision nestlings), may provide more consistent explanations for these patterns.     

Quail and rain in semiarid rangelands: Does management matter?

Rainfall is a strong driver of quail populations on southwestern rangelands and can account for a large portion (~70–95%) of the variability in regional quail production and abundance. Landowners have attempted to moderate these boom-and-bust fluctuations via management; however, presently it is unknown whether management can increase or stabilize quail populations in semiarid environments or whether rainfall remains as influential at small spatial extents. Our objectives were to evaluate the efficacy of management at mitigating the effects of rainfall on northern bobwhite (Colinus virginianus) populations on semiarid rangelands and to quantify the influence of rainfall on bobwhite density at smaller spatial extents. We conducted a study to evaluate these objectives during 2014–2020 in the Rio Grande Plains (n = 11 sites; 1,100‒6,500 ha) and Rolling Plains (n = 4 sites; 1,900‒4,000 ha) of Texas, USA. We estimated bobwhite density during late autumn (Dec‒Jan) on all sites using helicopter surveys within a distance-sampling framework. We also obtained site-level seasonal rainfall (Apr‒Aug) and quantified management intensity via landowner surveys and a scoring rubric to categorize sites into 3 classes (low, medium, and high management intensity). Bobwhite populations during this study experienced a boom-bust cycle in both the Rio Grande Plains and Rolling Plains, with mean bobwhite density fluctuating considerably (0.57‒2.96 bobwhites/ha and 0.02‒2.88 bobwhites/ha, respectively). In the Rio Grande Plains, mean bobwhite density significantly increased from low to high management intensity in 2015 (1.12 ± 0.17 bobwhites/ha vs. 2.87 ± 0.39 bobwhites/ha, respectively), 2016 (1.06 ± 0.20 bobwhites/ha vs. 2.96 ± 0.36 bobwhites/ha, respectively), 2017 (0.73 ± 0.16 bobwhites/ha vs. 1.91 ± 0.32 bobwhites/ha, respectively), and 2019 (0.42 ± 0.14 bobwhites/ha vs. 1.01 ± 0.26 bobwhites/ha, respectively; P < 0.05). In addition, rainfall at the site level accounted for a low amount of the variation in bobwhite density (r² = 0.09; P < 0.01). Similarly, in the Rolling Plains, mean bobwhite density significantly increased from low to high management intensity in 2015 (1.30 ± 0.27 bobwhites/ha vs. 2.20 ± 0.29 bobwhites/ha, respectively) and 2016 (1.26 ± 0.26 bobwhites/ha vs. 2.88 ± 0.34 bobwhites/ha, respectively; P < 0.05). Rainfall at the site level also accounted for a low amount of the variation in bobwhite density (r² < 0.02; P = 0.82). Our findings suggest that management can increase bobwhite density beyond that of less-managed properties but does not completely eliminate inter-annual fluctuations in semiarid environments. In addition, rainfall appears to exert less of an influence on bobwhite density at a site level (e.g., 2,000 ha) than has been documented at a regional level (e.g., ≥8 million ha).     

Does spring ice cover influence nest initiation date and clutch size in common eiders?

Understanding how environmental factors affect ecological parameters is important to understanding and predicting impacts of environmental change. Given evidence and anticipated impacts of climate variability, this is especially true with respect to sea ice and its role in animal life history in northern regions. We examined relationships between the extent of consolidated spring ice cover (pack and landfast), nest initiation and clutch size in common eiders (Somateria mollissima) in northern Labrador, a sub-Arctic region on the east coast of Canada. Our initial prediction was that eiders would delay nesting and have smaller clutches in years with more extensive spring ice cover. Between 1998 and 2003, we surveyed coastal islands for breeding eiders and collected information on nest age and clutch size. For those years, we estimated ice cover based on Radarsat-1 images supplied by the Canadian Ice Service during the spring period (approximately June 7–12). We found that spring ice cover was a significant positive predictor of nest initiation date, and the regression equation indicated that if the average extent of ice cover around nesting islands increased by 18 ha, average nesting date was delayed by approximately 1 day. Nest initiation date was a significant negative predictor of clutch size, and the regression equation indicated that a 20 day delay in nesting reduced average clutch size by approximately 1 egg. However, ice cover itself was not a significant predictor of clutch size. Our findings suggest that eiders breed when ice is present, but ice extent may negatively influence aspects of their breeding ecology.     

Age-specific nest-site preference and success in eiders

Variation in nest concealment is puzzling given the expected strong selection for safe nest sites. Selecting a concealed nest may decrease the risk of clutch predation but hinder parents from escaping predators, providing a possible solution to this paradox. Because the relative value of current versus future reproduction may vary with breeder age or state, nest concealment may also vary as a function of these attributes. We tested four predictions of the female and clutch safety trade-off hypothesis in eiders (Somateria mollissima): (1) nest concealment is negatively related to escape possibilities, (2) our capture rate of females is higher in covered nests, (3) egg predation is higher in open nests, and (4) overall nest success is unrelated to nest habitat. We also analysed nest microhabitat preferences and nest success relative to breeder age and body condition, controlling for nest spatial centrality. As expected, nest concealment and potential escape angle were negatively related, and capture by us, indicating female predation vulnerability, increased with nest cover. Clutch size was smaller in open nests, suggesting higher partial clutch predation, while it was larger among experienced and good-condition breeders. The probability of successful hatching was unrelated to nest habitat, positively associated with breeder experience, and negatively associated with hatching date. Experienced females selected more concealed and centrally located nests without sacrificing potential escape angles. The age-specific spatial distribution of nests on islands was unrelated to nest initiation dates, indicating no apparent competition. The age-specific preference of eiders for concealed nests may reflect declining reproductive value with age or confidence in surviving despite selecting a concealed nest. The apparently positive relationship between female age and survival and fecundity in eiders refutes the former alternative. Individual improvement in choosing safe nest sites, coupled with differential survival of individuals performing well, most likely explains age-specific nest-site preference and success.