Timing,frequency, and duration of incubation recesses in dabbling ducks

Nest attendance is an important determinant of avian reproductive success, and identifying factors that influence the frequency and duration of incubation recesses furthers our understanding of how incubating birds balance their needs with those of their offspring. We characterized the frequency and timing (start time, end time, and duration) of incubation recesses for mallard (Anas platyrhynchos) and gadwall (Mareca strepera) hens breeding in Suisun Marsh, California, USA, and examined the influences of day of year, ambient temperature at the nest, incubation day, and clutch size on recess frequency and timing using linear mixed models. Mallard, on average, took more recesses per day (1.69 ± 0.80, mean ± standard deviation) than did gadwall (1.39 ± 0.69), and 45% of mallard nest‐days were characterized by two recesses, while only 27% of gadwall nest‐days were characterized by two recesses. Mallard morning recesses started at 06:14 ± 02:46 and lasted 106.11 ± 2.01 min, whereas mallard afternoon recesses started at 16:39 ± 02:11 and lasted 155.39 ± 1.99 min. Gadwall morning recesses started at 06:30 ± 02:46 and lasted 91.28 ± 2.32 min, and gadwall afternoon recesses started at 16:31 ± 01:57 and lasted 192.69 ± 1.89 min. Mallard and gadwall started recesses earlier in the day with increasing ambient temperature, but later in the day as the season progressed. Recess duration decreased as the season progressed and as clutch size increased, and increased with ambient temperature at the nest. The impending darkness of sunset appeared to be a strong cue for ending a recess and returning to the nest, because hens returned to their nests earlier than expected when recesses were expected to end after sunset. Within hens, the timing of incubation recesses was repeatable across incubation days and was most repeatable for mallard afternoon recesses and on days in which hens took only one recess. Hens were most likely to be away from nests between 04:00 and 07:00 and between 16:00 and 19:00; therefore, investigators should search for nests between 07:00 and 16:00. Our analyses identified important factors influencing incubation recess timing in dabbling ducks and have important implications for nest monitoring programs.     

Notes on the breeding biology of the Sichuan Treecreeper (Certhia tianquanensis)

The Sichuan Treecreeper, Certhia tianquanensis Li 1995, was recently recognized as an independent species. Apparently, it is an endemic relict occupying an extremely small range in western Sichuan and Shaanxi provinces, China. During April–July 2003, its breeding biology was studied using field observation and data logger records of five nests found on Wawu Shan in Sichuan province, southwest China. Nest materials were mainly mosses; eggs are white with dense red spots concentrated at the large pole. During the incubation period, the male fed the female outside the nest with 6–13 min intervals between the single feeding events; afterwards, the female regularly returned to the nest within 47.8 ± 25.2 s. The female took 22.14 ± 3.24 recesses per day, with the mean recess length of 8.18 min throughout the incubation period. After the nestlings hatched, the female went out more often than during the incubation period: 55 and 56 times during the first 2 days of nestling period (off-nest time of 6.55 ± 3.15 min). Both parents fed the nestlings.     

Effects of down collection on incubation temperature, nesting behaviour and hatching success of common eiders (Somateria mollissima) in west Iceland

Incubating common eiders (Somateria mollissima) insulate their nests with down to maintain desirable heat and humidity for their eggs. Eiderdown has been collected by Icelandic farmers for centuries, and down is replaced by hay during collection. This study determined whether down collecting affected the female eiders or their hatching success. We compared the following variables between down and hay nests: incubation temperature in the nest, incubation constancy, recess frequency, recess duration, egg rotation and hatching success of the clutch. Temperature data loggers recorded nest temperatures from 3 June to 9 July 2006 in nests insulated with down (n = 12) and hay (n = 12). The mean incubation temperatures, 31.5 and 30.7°C, in down and hay nests, or the maximum and minimum temperatures, did not differ between nest types where hatching succeeded. Cooling rates in down, on average 0.34°C/min and hay nests 0.44°C/min, were similar during incubation recesses. Females left their nests 0–4 times every 24 h regardless of nest type, for a mean duration of 45 and 47.5 min in down and hay nests, respectively. The mean frequency of egg rotation, 13.9 and 15.3 times every 24 h, was similar between down and hay nests, respectively. Hatching success adjusted for clutch size was similar, 0.60 and 0.67 in down and hay nests. These findings indicate that nest down is not a critical factor for the incubating eider. Because of high effect sizes for cooling rate and hatching success, we hesitate to conclude that absolutely no effects exist. However, we conclude that delaying down collection until just before eggs hatch will minimize any possible effect of down collection on females.     

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.     

Breeding biology of White‐rumped Tanagers in central Brazil

ABSTRACT White‐rumped Tanagers (Cypsnagra hirundinacea) are widely distributed in northern Brazil, Bolivia, and Paraguay, and are classified as vulnerable in the state of Paraná and as endangered in the state of São Paulo, Brazil. Little is currently known about their breeding biology. We studied the breeding behavior of White‐rumped Tanagers in the Cerrado (Neotropical savanna) in central Brazil from 2002 to 2007. The breeding period extended from mid‐August to mid‐December. Nests were cup‐shaped and located mainly in trees of the genus Kielmeyera at a mean height of 3.7 ± 0.3 m (SE). Clutch sizes varied from one to three eggs and the incubation period lasted an average of 16.0 ± 0.3 d. Incubation was by females only and started with the laying of the first egg. Mean nest attentiveness (percent time on nests by females) was 64 ± 0.08%. Nestlings were fed by males, females, and, when present, helpers. The mean rate of food delivery rate to nests was 5.2 ± 0.4 items/h, with rates similar for males (mean = 2.7 ± 0.3 items/h) and females (mean = 2.4 ± 0.3 items/h). The mean duration of the nestling period was 12.1 ± 0.5 d. Compared to many temperate species of tanagers, White‐rumped Tanagers in our study had relatively small clutches, low nest attentiveness, and long incubation periods. As with other tropical species, such characteristics might be due to food limitation or high rates of nest predation.     

桂西南褐翅鸦鹃的孵卵行为与节律

2016年3~6月,在广西西南部龙州县弄岗村(22°26′35.20′′~22°30′46.90′′N,106°57′46.35′′~107°03′32.99′′E),通过野外观察和自动温度记录仪相结合的方法对褐翅鸦鹃(Centropus sinensis)的孵卵行为与节律进行了研究。结果表明,1)褐翅鸦鹃边筑巢边产卵,每2 d产1枚卵,卵长径和短径分别为(36.11±0.42)mm和(28.46±0.38)mm,卵重(16.35±0.51)g(n=44枚)。窝卵数3~5枚,孵卵期为(16.75±1.65)d(n=4巢),孵化率为45.45%(n=44枚)。孵卵期与窝卵数之间无显著相关性(r=0.865,P0.05);2)白天双亲共同参与孵卵,夜晚则由其中1只负责。夜间亲鸟的在巢时间从19时左右持续至翌日晨6时左右;3)亲鸟采取离巢次数少和离巢时间长的孵卵策略。亲鸟日活动时间在700 min以上(n=45 d),日离巢次数为(8.82±0.34)次(n=45 d),平均每次离巢持续时间为(52.91±2.35)min(n=397次),每次离巢持续时间与环境温度呈显著负相关关系(r=﹣0.113,P0.05);4)巢内平均孵卵温度为(31.7±0.3)℃(n=4巢),随孵卵天数增加而增加,并与环境温度(最高温r=0.566,最低温r=0.537,平均温r=0.706,P0.01)和日活动时间正相关(r=0.506,P0.01);5)有延迟孵卵行为。延迟孵卵期间夜晚巢内最低温是22.1℃。在桂西南北热带气候环境中,高的环境温度是保障褐翅鸦鹃孵卵成功的主要因素之一。     

Communal nesting under climate change: fitness consequences of higher incubation temperatures for a nocturnal lizard

Communal nesting lizards may be vulnerable to climate warming, particularly if air temperatures regulate nest temperatures. In southeastern Australia, velvet geckos Oedura lesueurii lay eggs communally inside rock crevices. We investigated whether increases in air temperatures could elevate nest temperatures, and if so, how this could influence hatching phenotypes, survival, and population dynamics. In natural nests, maximum daily air temperature influenced mean and maximum daily nest temperatures, implying that nest temperatures will increase under climate warming. To determine whether hotter nests influence hatchling phenotypes, we incubated eggs under two fluctuating temperature regimes to mimic current ‘cold’ nests (mean = 23.2 °C, range 10–33 °C) and future ‘hot’ nests (27.0 °C, 14–37 °C). ‘Hot’ incubation temperatures produced smaller hatchlings than did cold temperature incubation. We released individually marked hatchlings into the wild in 2014 and 2015, and monitored their survival over 10 months. In 2014 and 2015, hot‐incubated hatchlings had higher annual mortality (99%, 97%) than cold‐incubated (11%, 58%) or wild‐born hatchlings (78%, 22%). To determine future trajectories of velvet gecko populations under climate warming, we ran population viability analyses in Vortex and varied annual rates of hatchling mortality within the range 78– 96%. Hatchling mortality strongly influenced the probability of extinction and the mean time to extinction. When hatchling mortality was >86%, populations had a higher probability of extinction (PE: range 0.52– 1.0) with mean times to extinction of 18–44 years. Whether future changes in hatchling survival translate into reduced population viability will depend on the ability of females to modify their nest‐site choices. Over the period 1992–2015, females used the same communal nests annually, suggesting that there may be little plasticity in maternal nest‐site selection. The impacts of climate change may therefore be especially severe on communal nesting species, particularly if such species occupy thermally challenging environments.     

Function of egg punctures by Shiny Cowbirds in parasitized and nonparasitized Creamy‐bellied Thrush nests

ABSTRACT Avian brood parasites usually remove or puncture host eggs. Several hypotheses have been proposed to explain the function of these behaviors. Removing or puncturing host eggs may enhance the efficiency of incubation of cowbird eggs (incubation‐efficiency hypothesis) or reduce competition for food between cowbird and host chicks in parasitized nests (competition‐reduction hypothesis) and, in nonparasitized nests, may force hosts to renest and provide cowbirds with new opportunities for parasitism when nests are too advanced to be parasitized (nest‐predation hypothesis). Puncturing eggs may also allow cowbirds to assess the development of host eggs and use this information to decide whether to parasitize a nest (test‐incubation hypothesis). From 1999 to 2002, we tested these hypotheses using a population of Creamy‐bellied Thrushes (Turdus amaurochalinus) in Argentina that was heavily parasitized by Shiny Cowbirds (Molothrus bonariensis). We found that 56 of 94 Creamy‐bellied Thrush nests (60%) found during nest building or egg laying were parasitized by Shiny Cowbirds, and the mean number of cowbird eggs per parasitized nest was 1.6 ± 0.1 (N= 54 nests). At least one thrush egg was punctured in 71% (40/56) of parasitized nests, and 42% (16/38) of nonparasitized nests. We found that cowbird hatching success did not differ among nests where zero, one, or two thrush eggs were punctured and that the proportion of egg punctures associated with parasitism decreased as incubation progressed. Thus, our results do not support the incubation‐efficiency, nest‐predation, or test‐incubation hypotheses. However, the survival of cowbird chicks in our study was negatively associated with the number of thrush chicks. Thus, our results support the competition‐reduction hypothesis, with Shiny Cowbirds reducing competition between their young and host chicks by puncturing host eggs in parasitized nests.     

Nest attendance by tropical and temperate passerine birds: Same constancy,different strategy

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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.     

Incubation failure and nest abandonment by Leach's Storm‐Petrels detected using PIT tags and temperature loggers

ABSTRACT The nocturnal activity of burrow‐nesting seabirds, such as storm‐petrels and shearwaters, makes it difficult to study their incubation behavior. In particular, little is known about possible differences in the incubation behavior of adults at successful and unsuccessful nests. We combined the use of passive integrated transponder (PIT) technology and nest‐temperature data loggers to monitor the incubation behavior of 10 pairs of Leach's Storm‐Petrels (Oceanodroma leucorhoa). The mean incubation bout length was 3.31 ± 0.59 (SD) days for individual adults at successful nests (N= 4) and 1.84 ± 1.16 d for individuals at unsuccessful nests (N= 6). Mean bout length for pairs in successful burrows (3.51 ± 0.56 d) did not differ significantly (P= 0.07) from that for pairs in unsuccessful burrows (1.80 ± 1.20 d), perhaps due to one failed nest with a high mean bout length (4.15 d). The total number of incubation bouts per parent (4.3 ± 1.9 bouts) did not differ with hatching success. Adults whose nests failed repeatedly exhibited truncated incubation bouts (< 12 h) prior to complete nest failure and were more likely than successful parents to make brief visits to nearby, occupied nesting burrows. Our results suggest that the decision by Leach's Storm‐Petrels to abandon a nest is not an abrupt one. Rather, failed nesting attempts may be characterized by truncated incubation bouts where individuals pay the energetic cost of travel to and from the burrow, but do not remain long enough to successfully incubate the egg.     

Movements of female Sage Grouse Centrocercus urophasianus during incubation recess

We combined GPS data‐loggers, VHF transmitters and DVR video‐monitoring to measure fine‐scale movement patterns during daily incubation recesses by female Sage Grouse Centrocercus urophasianus, a species with uniparental incubation that has experienced widespread population decline and distributional contraction. Most (69.6%) Sage Grouse recess activity was highly localized within a core recess area averaging 2.58 ± 0.64 ha, and females remained within 242.3 ± 30.0 m from the nest during recesses (total recess areas were 11.06 ± 2.27 ha). Visually conspicuous Sage Grouse movements near nests at the start and end of recesses and consistent occupation of core recess areas point to a mechanism for newly abundant predators such as the Northern Raven Corvus corax to detect and depredate Sage Grouse nests. Our methods apply to other avian species of scientific interest and conservation concern.     

Intraspecific nest parasitism in the grey starling (Sturnus cineraceus)

We studied intraspecific nest parasitism in the grey starling (Sturnus cineraceus) in 1992 and 1993. We used three criteria to detect nest parasitism: (i) the appearance of more than one egg per day while the host was laying; (ii) the appearance of extra eggs after the host completed its clutch; and (iii) the appearance of eggs which were of a different shape, size and color to other eggs in the clutch. There were 290 nests (157 nests in 1992; 133 nests in 1993) in which the clutch was completed early (clutches initiated before May 10). Twenty-nine (1992) and 32 (1993) nests contained at least one parasitic egg. Parasitic eggs hatched if they were laid during the laying period and early in the incubation period of their host, and a few of them fledged. Fledging success of parasitic eggs was not different from that of eggs in non-parasitized nests if parasitic eggs were laid during the host's laying period. However, fledging success of all parasitic eggs was fewer than that of eggs in non-parasitized nests. By comparison, fledging success of parasitized nests was not a great as that of non-parasitized nests.     

Environmentally induced variation in body size of turtles hatching in natural nests

Eggs from three snapping turtles (Chelydra serpentina) were divided between two natural nests in a factorial experiment assessing the role of the nest environment as a cause for variation in body size and energy reserves of hatchlings at our study site in northcentral Nebraska. Nest # 1 was located in an unshaded area on the south side of a high sandhill, whereas nest #2 was located in an unshaded area on level ground. Eggs in nest #1 increased in mass over the course of incubation, with eggs at the bottom of the nest gaining more mass than eggs nearer to the surface. In constrast, eggs in nest #2 lost mass during incubation, with eggs at the bottom declining less in mass than eggs at the top of the cavity. Hatchlings from nest #1 were much larger (but contained smaller masses of unused yolk) than hatchlings from nest #2. Additionally, eggs from the lower layers in both nests tended to produce larger hatchings (but with smaller masses of unused yolk) than eggs from the upper layers. Thus, ecologically important variation in body size and nutrient reserves of hatchling snapping turtles results from variation in the environment among and within nests.     

Nest construction by a ground-nesting bird represents a potential trade-off between egg crypticity and thermoregulation

Predation selects against conspicuous colors in bird eggs and nests, while thermoregulatory constraints select for nest-building behavior that regulates incubation temperatures. We present results that suggest a trade-off between nest crypticity and thermoregulation of eggs based on selection of nest materials by piping plovers (Charadrius melodus), a ground-nesting bird that constructs simple, pebble-lined nests highly vulnerable to predators and exposed to temperature extremes. Piping plovers selected pebbles that were whiter and appeared closer in color to eggs than randomly available pebbles, suggesting a crypsis function. However, nests that were more contrasting in color to surrounding substrates were at greater risk of predation, suggesting an alternate strategy driving selection of white rocks. Near-infrared reflectance of nest pebbles was higher than randomly available pebbles, indicating a direct physical mechanism for heat control through pebble selection. Artificial nests constructed of randomly available pebbles heated more quickly and conferred heat to model eggs, causing eggs to heat more rapidly than in nests constructed from piping plover nest pebbles. Thermal models and field data indicated that temperatures inside nests may remain up to 2–6°C cooler than surrounding substrates. Thermal models indicated that nests heat especially rapidly if not incubated, suggesting that nest construction behavior may serve to keep eggs cooler during the unattended laying period. Thus, pebble selection suggests a potential trade-off between maximizing heat reflectance to improve egg microclimate and minimizing conspicuous contrast of nests with the surrounding substrate to conceal eggs from predators. Nest construction behavior that employs light-colored, thermally reflective materials may represent an evolutionary response by birds and other egg-laying organisms to egg predation and heat stress. An erratum to this article can be found at     

Sooty Falcon Falco concolor reproduction and population dynamics on the islands in the Sea of Oman

Knowledge of demographic parameters affecting population dynamics is critical to the formulation of effective conservation strategies. Sooty Falcon Falco concolor is a little‐studied, Near‐threatened species; estimates of global population size and trend for this species are uncertain. They lay eggs during mid‐summer and sometimes nest in colonies. This unusual breeding ecology suggests that demographic parameters driving their population growth rate may differ from those of most other falcons. We studied Sooty Falcon reproduction at breeding aggregations on Fahal Island and the Daymaniyat islands in the Sea of Oman during 2007–2014, modelled population growth and identified important life history parameters using elasticity analysis. The mean (± se) clutch and brood size was 2.83 ± 0.06 and 2.11 ± 0.07, respectively. Overall, 11.7% of nests failed between the egg and nestling stages, and the failure rate differed significantly between Fahal and the Daymaniyats, and across years. The mean proportion of eggs that hatched annually was 0.66 ± 0.02, and broods were significantly smaller on the Daymaniyats than on Fahal. Falcons on Fahal Island had a higher rate of hatching, a higher rate of nests that produced at least one chick, and produced more chicks per nest than on the Daymaniyats. We suggest that Fahal's proximity to the mainland gives breeding Sooty Falcons access to a more plentiful and stable source of food, especially during the period between arrival from the wintering grounds and the onset of the autumn migration of prey birds, resulting in the better reproductive rates for falcons on Fahal Island, relative to those on the Daymaniyat Islands. The annual asymptotic population growth rate (λ) was 0.87 (95% confidence interval (CI) 0.75–0.99), suggesting a declining population, although Sooty Falcons enjoyed a slightly higher population growth rate on Fahal than on the Daymaniyats. Because our study population is on the edge of the breeding range and is isolated from other breeding areas, measures to improve reproductive success of Sooty Falcons breeding on the islands in the Sea of Oman could be important for conservation of Sooty Falcons in Oman.     

Nest position,breeding success and diet of the Black-crowned Night Heron,Nycticorax nycticorax in the Anzali Wetland,Northern Iran (Aves: Ardeidae)

Breeding ecology of the Black-crowned Night Heron (Nycticorax nycticorax) was studied in a mono-specific colony in the Anzali wetland, Northern Iran during the breeding season of 2016. The breeding period lasted from mid-May to late July. The average clutch size was 3.1±0.6 eggs and the breeding success 77.6%. No significant differences were found between nests built on trunks and those built on branches of trees. The clutch size and breeding success appeared to be independent of the structural variables of the nesting site (diameter of trees, height from the ground, height of nests from the canopy, nest number per tree, location of nests on trunks and branches). No significant difference was found between the timing of the start of incubation and the height of nests above the ground. The average vertical and horizontal distances between nests was one metre. Fish, particularly Carassius gibelio, dominated the diet of the nestlings.     

Nesting biology and food habits of the endangered Sakalava Rail Amaurornis olivieri in the Mandrozo Protected Area,western Madagascar§

We studied the nesting biology and food habits of the endangered and endemic Sakalava Rail Amaurornis olivieri from July to November 2015 in the Mandrozo Protected Area, western Madagascar. Three nesting pairs were observed and their nests were constructed in a dense mat of reeds Phragmites mauritianus and averaged 56.7 ± 15.3 cm above the water (n = 3 nests). Nests were built by both adults and it took 3 d on average to complete a nest (n = 2 nests). Thirteen matings were observed and lasted 4.1 s on average (n = 2 pairs). Average clutch size was three eggs (n = 2 nests). Both sexes incubated; the incubation period was 15–17 d (n = 2 nests). Both male and female participated in brooding and feeding the young, which remained for 3 d in the nest and became independent of their parents at 45 d of age. Based on 194 identified food items, the Sakalava Rail’s diet was composed of invertebrates: spiders (53.1%), insects (32%), crustaceans (10.8%) and molluscs (4.1%). The home ranges of two radio-tagged individuals were 0.95 and 1.98 ha.     

Breeding ecology of Red‐faced Cormorants in the Pribilof Islands,Alaska

ABSTRACT Red‐faced Cormorants (Phalacrocorax urile) are North Pacific endemics recognized as a vulnerable species, but little is known about their breeding ecology. We studied Red‐faced Cormorants on St. Paul Island, Alaska, from 1975 to 2009, with more detailed data collected in 2004 and 2005. Mean clutch sizes in 2004 (3.2 ± 0.8 [SD] eggs) and 2005 (3.1 ± 0.8 eggs) were similar to the long‐term average (2.9 ± 0.3 eggs from 1976 to 2009). The mean laying interval in 2004 and 2005 was 2.15 ± 0.80 d (N= 407), and the mean egg period (number of days between laying of an egg and hatching) was 31.1 ± 1.4 d (N= 158). Approximately 64 ± 17% of eggs hatched during the period from 1975 to 2009. The mean number of chicks per nest in 2004 and 2005 was 2.8 ± 0.8 (N= 232), and the mean number of fledglings per initiated nest in all years was 1.22 ± 0.52. Chicks fledged 46 to 66 d posthatching. In 2004 and 2005, the primary causes of egg loss were predation by Arctic foxes (Vulpes lagopus) and destruction of eggs and abandonment of nests due to storms. Starvation was the primary cause of nestling mortality in both years. Because chicks are dependent on parents to provide food for over 45 d, consistent near‐shore foraging opportunities must be available. From 1975 to 2009, Red‐faced Cormorants experienced only 1 yr of complete reproductive failure (1984). The consistent reproductive success of Red‐faced Cormorants suggests that conditions may be relatively stable for this species on St. Paul Island, or that the variability in their breeding ecology (e.g., phenology, clutch sizes, and incubation strategies) provides the flexibility needed to successfully fledge some chicks nearly every year.     

Costs and response to conspecific brood parasitism by colonial red-breasted mergansers

Costs of conspecific brood parasitism (CBP) are expected to be influenced by a species’ life history traits. Precocial birds lay large clutches, and clutches that have been enlarged by CBP can affect host fitness through a longer incubation period, displaced eggs, and lower hatching success. We examined costs and response to CBP by hosts in a population of colonial red-breasted mergansers (Mergus serrator; n?=?400 nests over 8 years) within which 29% of parasitized clutches were enlarged considerably (≥?15 eggs). Length of the incubation period did not increase with clutch size. The mean number of eggs displaced from a parasitized nest during incubation (2.8) was 2×?greater than at an unparasitized nest (1.4). Hatching success declined by 2% for each additional egg in the nest. Thus, for a nest with?≥?15 eggs, one or more fewer host eggs hatch relative to an unparasitized nest with the same number of host eggs, assuming equal probability of success for all eggs. Hosts were 40% more likely to desert nests receiving 2 or 6 experimental eggs relative to unparasitized control nests, although it is unknown whether hens deserting a nest renested elsewhere. Our study indicates that costs of CBP to hosts during nesting may be limited to those red-breasted mergansers incubating the largest clutches (≥?15 eggs), and it raises questions about the adaptive significance of deserting a parasitized clutch.