The cost of egg production: increased egg production reduces future fitness in gulls

Measurements of costs of reproduction are essential for our understanding of the evolution of reproductive effort. While in birds the effects of increased chick-rearing effort on subsequent survival and fecundity have been relatively well studied experimentally, costs associated with increased egg-production effort have received relatively little attention. We experimentally increased the egg-production effort of individually marked Lesser Black-backed Gulls Larus fuscus and followed their breeding performance in the next year. In the season following increased egg production, females, but not males, were less likely to be resighted in the study plot and those that did return were less likely to produce a clutch compared to control birds. It is unclear whether the observed effect on local return rate represents differential survival, differences in breeding propensity or differences in dispersal between experimental and control females. In any event, all of these would adversely affect the fitness of experimental females. In addition, those experimental females that did breed invested less in egg production the following season, which again is likely to affect breeding performance. Thus, this study provides evidence that there is an inter-brood trade-off between current egg-production effort and future fitness in birds.     

Breeding Propensity of Female Harlequin Ducks

Abstract: Breeding propensity, the proportion of sexually mature females that initiate egg production, can be an important demographic trait when considering reproductive performance and, subsequently, population dynamics in birds. We measured egg production using yolk precursor (vitellogenin and very-low-density lipoprotein) analyses and we measured nesting using radiotelemetry to quantify breeding propensity of adult female harlequin ducks (Histrionicus histrionicus) in British Columbia, Canada, in 2003 and 2004. Using both methods combined, and accounting for error rates of each, we estimated that breeding propensity of adult females that migrated to breeding streams was 92%. These data suggest that, despite speculation that harlequin ducks have low breeding propensity, almost all adult females on our study site were not constrained in their ability to produce eggs and that influences on reproductive performance at later stages likely have much stronger effects on population dynamics.     

FACTORS AFFECTING THE AGE OF FIRST BREEDING OF THE KITTIWAKE RISSA TRIDACTYLA

At a Kittiwake colony in Northumberland, 80% of those birds which returned to their natal colony to breed were males and these supplied 52% of all male recruits. More females breed away from their natal colony than males. There was no differences in the proportions of young fledged from sites in the centre or at the edge of the colony, or by parents of different experience, which returned to breed. Kittiwakes breed for the first time at ages from 3 to 8 years, but most at 4 or S years old. Males arrive back at the colony at an earlier age than females and breed for the first time one year earlier. Males obtaining sites at the centre of the colony first breed at an earlier age than those at the edges. Neither the age nor the area of first breeding appear to be transmitted from parent to offspring. Males breeding first aged 4 years or younger produced more young than those which first bred aged 5 years or older, despite their partners laying smaller clutches. This difference was most marked among those males recruited to sites in the centre of the colony. The advantage of this earlier breeding is counteracted by a lower survival rate among those males which start to breed at the younger ages. In all breeding Kittiwakes, annual reproductive output increases with experience while annual survival rates decrease. Once they had started to breed, many birds failed to breed in one subsequent season. Nearly 60% of these cases of intermittent breeding occurred in the year following first breeding. Intermittent breeding was most frequent among young birds and among females. It is suggested that each breeding involves a cost to the individual in terms of reduced survival, and that deferred and intermittent breeding are means of guarding survival. A model is proposed whereby the age at which a bird starts to breed, the nesting site which it obtains, and its subsequent breeding strategy result in each individual producing an optimal number of reproducing offspring in its lifetime, relative to its quality.     

Covariation among demographic and climate parameters in whiskered auklets Aethia pygmaea

Annual survival rate and other demographic parameters of whiskered auklets Aethia pygmaea , a small planktivorous seabird, were measured at Buldir Island Alaska during 1992–2003 to provide comparative information for auk life history studies and to test for links among climate, age, productivity and survival. Using two 9  m mistnets, we captured and recaptured 384 adult and 193 sub-adult (one year old, a known-age component of our sample) birds as they arrived at the colony after dark during May and June (1,730  capture events). The best fitting model indicated a lower initial survival rate over the first year following marking (0.708±0.036 SE), and subsequent survival (mean 0.835±0.029) covarying with the Aleutian Low Pressure climate Index, with higher auklet survival in years with weak low pressure over the Aleutian Islands. Annual survival rate varied from 0.726±0.127 in 1998–99 to 0.994±0.077 in 1994–95, rates similar to those previously reported for least A. pusilla and crested auklets A. cristatella . A model based only on recaptures of known-age birds indicated a lower local survival estimate over the first year following marking (age one to two years), with no other age-effects on survival. Breeding propensity by age inferred from recaptures of birds with fully-developed brood patches that were originally marked as sub-adults (one year olds) indicated 53% breeding at age two, 94% breeding at age 3, 97% breeding at age 4 and 100% breeding thereafter. The sex ratio of the sampled birds was significantly male biased (60/40), likely due to differences in behaviour between males and females during the incubation stage. Taken together, our data indicate that whiskered auklet survival and productivity covaried with continuous variation in large-scale climatic conditions, the mechanism being either negative effects of stormy North Pacific weather or indirect effects on food supplies.     

Trade-off between current reproductive effort and delay to next reproduction in the leatherback sea turtle

The trade-off between current and future reproduction plays an important role in demographic analyses. This can be revealed by the relationship between the number of years without reproduction and reproductive investment within a reproductive year. However, estimating both the duration between two successive breeding season and reproductive effort is often limited by variable recapture or resighting effort. Moreover, a supplementary difficulty is raised when nonbreeder individuals are not present sampling breeding grounds, and are therefore unobservable. We used capture–recapture (CR) models to investigate intermittent breeding and reproductive effort to test a putative physiological trade-off in a long-lived species with intermittent breeding, the leatherback sea turtle. We used CR data collected on breeding females on Awa:la-Ya:lima:po beach (French Guiana, South America) from 1995 to 2002. By adding specific constraints in multistate (MS) CR models incorporating several nonobservable states, we modelled the breeding cycle in leatherbacks and then estimated the reproductive effort according to the number of years elapsed since the last nesting season. Using this MS CR framework, the mean survival rate was estimated to 0.91 and the average resighting probability to 0.58 (ranged from 0.30 to 0.99). The breeding cycle was found to be limited to 3 years. These results therefore suggested that animals whose observed breeding intervals are greater than 3 years were most likely animals that escaped detection during their previous nesting season(s). CR data collected in 2001 and 2002 allowed us to compare the individual reproductive effort between females that skipped one breeding season and females that skipped two breeding seasons. These inferences led us to conclude that a trade-off between current and future reproduction exists in leatherbacks nesting in French Guiana, likely linked to the resource provisioning required to invest in reproduction.     

Arrival fat and reproductive performance in a long-distance passerine migrant

Long-distance passerine migrants deposit substantial fat stores to fuel their migratory journey. Many of those migratory birds arrive at their northerly breeding grounds with larger fat stores than were necessary to reach their breeding area. Both male and female American Redstarts ( Setophaga ruticilla) arrived to breed in Michigan's Upper Peninsula with fat, and females arrived with more fat than males in 2 out of 3 years. We test the hypothesis that migrants arriving at the breeding grounds with more body fat have higher reproductive success than birds arriving with little or no fat. Females, and to a lesser extent males, that arrive with fat experience gains in reproductive performance as evidenced by increased clutch size, egg volume, and nestling mass. The results have implications for understanding how events occurring during one phase of the annual cycle influence survival and/or reproductive performance in subsequent phases.     

Population dynamics in a long-lived seabird: I. Impact of breeding activity on survival and breeding probability in unbanded king penguins

Understanding the trade-off between current reproductive effort, future survival and future breeding attempts is crucial for demographic analyses and life history studies. We investigated this trade-off in a population of king penguins (Aptenodytes patagonicus) marked individually with transponders using multistate capture-recapture models. This colonial seabird species has a low annual proportion of non-breeders (13%), despite a breeding cycle which lasts over 1 year. To draw inferences about the consequences of non-breeding, we tested for an effect of reproductive activity on survival and on the probability of subsequent breeding. We found that birds non-breeding in year t show the same survival rate as breeders (two-states analysis: breeding and non-breeding). However, breeders had a lower probability of breeding again the following year. This negative phenotypic correlation suggests the existence of reproductive costs affecting future breeding probability, but it might also be strengthened by late arrival for courtship in year t. A three-state analysis including breeding success revealed that failed breeders in year t have a lower probability to reproduce successfully in year t + 1 than non-breeders in year t, providing some evidence for the existence of reproductive costs. Moreover, successful breeders showed higher survival probability. This positive phenotypic correlation between current reproduction and subsequent survival supports the hypothesis of an heterogeneity in individual quality. Males breeding in year t had a lower probability to breed again in year t + 1 than females, suggesting higher reproductive costs for this sex. Such additional costs might be due to higher male parental investment in the final phase of chick-rearing, which also delays the arrival of males in year t + 1, and decreases their breeding probability. Our study is the first to explore the breeding biology and the demography of penguins without the disturbance of flipper-bands.     

Increased survival and breeding performance of double breeders in little penguins Eudyptula minor,New Zealand: evidence for individual bird quality?

The little penguin Eudyptula minor is unique among penguin species in being able to fledge chicks from two clutches in one breeding season. Pairs laying two clutches in a given season make a higher reproductive investment, and may be rewarded by a higher reproductive success as they may raise twice as many chicks as pairs laying one clutch. The higher effort made by pairs laying two clutches could correlate negatively with survival, future reproductive performance or offspring survival, indicating a cost of reproduction. Conversely, a positive relationship between the number of clutches produced in a given breeding season and survival, future reproductive performance or offspring survival would indicate that birds laying two clutches belonged to a category of birds with higher fitness, compared to birds laying only one clutch in the season. In this study we used a long‐term data set taken from an increasing population of little penguins in Otago, SE New Zealand. We modelled the relationship between the number of clutches laid in a breeding season and survival probability, reproductive performance in the next breeding season and first year survival of offspring using capture‐recapture modelling.
Birds laying two clutches produced 1.7 times more fledglings during a breeding season than pairs laying one clutch. We found that birds laying two clutches had a higher probability of breeding in the following breeding season, a higher probability of laying two clutches in the following breeding season and a higher survival probability. There was no overall difference in post‐fledging survival between the young of birds producing one clutch and the young of birds producing two clutches. However, the survival of young of single clutch breeders declined with laying date, whereas the young of double clutch breeders had the same survival rate irrespective of laying date. For a subset of data with birds of known age, we found evidence that the probability of laying two clutches increased with age. However, there were also indications for differences among birds in the tendency to lay two clutches that could not be attributed to age. We tentatively interpret our results as evidence of quality difference among little penguin breeders.     

Breeding limits foraging time: evidence of interrupted foraging response from body mass variation in a tropical environment

Birds should store body reserves if starvation risk is anticipated; this is known as an ‘interrupted foraging response’. If foraging remains unrestricted, however, body mass should remain low to limit the predation risk that gaining and carrying body reserves entails. In temperate environments mass gain in female birds during breeding is often attributed to egg formation and mass loss after incubation to flight adaptation or the effect of reproductive workload, rather than as a result of an adaptive interrupted foraging response to the limited foraging time or unpredictable foraging conditions that breeding demands. In tropical environments, foraging conditions vary more within the breeding season than in temperate environments, and so studies in tropical environments are more suited to decouple the potentially confounded effects of increase in body reserves versus egg formation on the body mass of breeding birds. In this study, we test whether breeding results in an interrupted foraging response in a tropical savannah system using body mass data collected over a 15‐year period from female common bulbuls Pycnonotus barbatus. This species breeds both in the wet and dry season, despite fewer resources being available in the dry season. Breeding stage predicted female body mass: body mass peaked abruptly during incubation, but was not closely associated with the egg‐laying stage, and declined during brood rearing. Breeding females were heavier in the dry season than in the wet season. In the dry season, heavier birds were more likely to incubate eggs or brood chicks. These observations suggest that increased body reserves are required to buffer the consequence of limited foraging time or impoverished foraging conditions, which may be most pronounced during incubation and in the dry season, respectively. Such mass increases are consistent with an interrupted foraging response, which may apply to temperate zone birds experiencing foraging restrictions during breeding.     

BREEDING NUMBERS AND REPRODUCTIVE RATE OF EIDERS AT THE SANDS OF FORVIE NATIONAL NATURE RESERVE, SCOTLAND

The total population of Eiders at the Sands of Forvie National Nature Reserve, Aberdeenshire, increased from about 3000 birds during 1961–63 to about 4800 birds in 1964–70. At the same time the estimated number of breeding pairs increased from about 1200 in 1961–63, to about 1800 in 1965–68 and to 2000 in 1970. The mean size of completed clutches was 4.4; the number of eggs in a clutch showed a significant decline during the season from an average of 4.7 to 3.4 in most years. The overall hatching success was 63%, but there was a decline with season as a result of increased losses to predators. In 1964 and 1969 laying was retarded, mean clutch-size reduced, and the number of birds attempting to lay dropped by half, due to inclement weather just at the onset of laying. In 1969 the eggs produced were smaller than in other years, and hatching success was lower. The female incubates without feeding, and is required to store sufficient energy, in the form of fat, to last her through the 26 days in addition to producing her clutch of eggs. An hypothesis is advanced which relates the feeding efficiency of the paired female immediately prior to laying to her egg production and incubating pattern, and which offers an explanation of the decline in clutch-size and hatching success evident during the season. In most years less than 5% of hatchlings survived to fledge; high survival was recorded in 1963, 1968 and 1970. Following the high production in 1963 the population increased in 1964 and the breeding stock in 1965 (females start to breed at two years old). The corresponding changes, following good breeding in 1968, were not so clearly detected because of unusually high adult mortality from oil pollution at the winter grounds in 1968 and the ‘late’ breeding year in 1969. The breeding stock in 1970, however, was higher than in any other year. This population continues to grow apparently as a result of its own reproductive output checked only by low productivity in most years and occasional high adult mortality.     

Selection for synchronous breeding in the European starling

Colonial birds often demonstrate considerable breeding synchrony. In southern Sweden the semi-colonial European starling initiated the vast majority of clutches within one week. Laying dates were positively skewed so that many birds initiated clutches at similar dates early in the season. Breeding was further synchronised by a particularly strong clutch-size reduction equivalent to one third of an egg per day during the first part of the breeding season. The decline in clutch size with season also held true for separate age-classes of females, for individual females laying at different times at different years and for individual females laying at different times the same year. Trends in breeding success during nestling rearing were unlikely to explain the high degree of breeding synchrony or the seasonal decline in clutch size; nestling survival and growth were weakly related or unrelated to reproductive timing. In contrast recruitment success of fledged offspring declined sharply with season. Even within the synchronous laying period, defined as clutches initiated during the first week each year, local recruitment success declined. It is suggested that the early seasonal decline is caused by selection for synchronous fledging permitting the immediate formation of flocks after fledging, whereas the late seasonal trends may be caused by either population differences in female quality or deteriorating conditions for raising young.     

Age-specific variation in reproduction is largely explained by the timing of territory establishment in the New Zealand stitchbird Notiomystis cincta

1. Using data from 327 nests over a consecutive 8-year period we examined age-specific variation in reproduction in a population of stitchbirds (or hihi) Notiomystis cincta and related how differences in reproductive performance were linked to the timing of territory establishment and breeding. 2. Across the population all reproductive parameters showed a quadratic relationship with an increase mainly between the first and second breeding season and a decline after the fourth year. A longitudinal analysis showed evidence of senescence by the sixth year in the numbers of chicks fledged and recruited. 3. Reproductive increases between years 1 and 2 were the result of poor-quality females dying after their first breeding season (differential selection hypothesis) in combination with surviving females showing improvements in reproduction in their second year (individual improvement/constraint hypothesis). 4. There was no effect of mate experience or territory quality on improvements in breeding between years. 5. The key variable influencing reproductive output was the timing of breeding. Birds that started laying earlier were more likely to lay multiple clutches in any given season. This was the main difference between first-year and older birds; generally first-year birds initiated egg laying later and consequently laid fewer clutches. 6. Approximately half of all first-year birds did not establish their territory until after the breeding season had begun. This delay in territory establishment resulted in these birds delaying breeding, which resulted in them having a lower reproductive output relative to all other birds. First-year birds that managed to establish their territory before breeding commenced, had similar rates of reproduction as older birds. 7. There was a positive relationship between the timing of territory establishment during a female's first year and her hatching date in the previous breeding season. We hypothesize that this was because late-hatched females were less able to effectively compete for territories against earlier-hatched members of their cohort, and this delayed their establishment and breeding in their first year. Thus, this social constraint is likely to be a major factor driving age-specific reproductive variation in this population.     

THE EVOLUTION OF FEMALE BODY SIZE IN RED-WINGED BLACKBIRDS: THE EFFECTS OF TIMING OF BREEDING,SOCIAL COMPETITION,AND REPRODUCTIVE ENERGETICS

We examined opposing selective forces on female body size in the sexually dimorphic red-winged blackbird: social competition favoring larger females, and energetic advantages favoring smaller females. Downhower proposed that selection might drive female birds to be smaller than the optimum for survival, if smaller females were able to exceed their energetic requirements for self-maintenance earlier in the season and therefore breed earlier. Since in most birds the earliest breeders fledge the most young, this could favor the evolution of smaller female size, and therefore contribute to the magnitude of sexual size dimorphism in these birds. We tested this hypothesis in 1987 and 1988 by comparing the size and breeding date of female red-winged blackbirds. Consistent with our preditions, early-nesting females had much higher nesting success, but contrary to prediction, larger females bred earlier. We then examined the effects of female size on competition. If large females have an advantage in social competition, and if competition influences breeding date and reproductive success, then larger females might breed earlier. Primary females, the first females to arrive and nest on a territory, were more aggressive than lower ranked females; more aggressive females settled on better territories and laid earlier than less aggressive females; and larger females were more aggressive. Social competition between females may therefore favor large females. Finally, we tested the prediction that selection favoring large females might be limited by energetic constraints on large females. We found that large females had less fat than small females during breeding, and that the levels of fat that females of a given size carried affected breeding date and egg size. Therefore, social competition may favor large females, but reproductive energetics favoring smaller females may constrain selection for large female body size.     

Testing the reproductive and somatic trade‐off in female Columbian ground squirrels

Energetic trade‐offs in resource allocation form the basis of life‐history theory, which predicts that reproductive allocation in a given season should negatively affect future reproduction or individual survival. We examined how allocation of resources differed between successful and unsuccessful breeding female Columbian ground squirrels to discern any effects of resource allocation on reproductive and somatic efforts. We compared the survival rates, subsequent reprodction, and mass gain of successful breeders (females that successfully weaned young) and unsuccessful breeders (females that failed to give birth or wean young) and investigated “carryover” effects to the next year. Starting capital was an important factor influencing whether successful reproduction was initiated or not, as females with the lowest spring emergence masses did not give birth to a litter in that year. Females that were successful and unsuccessful at breeding in one year, however, were equally likely to be successful breeders in the next year and at very similar litter sizes. Although successful and unsuccessful breeding females showed no difference in over winter survival, females that failed to wean a litter gained additional mass during the season when they failed. The next year, those females had increased energy “capital” in the spring, leading to larger litter sizes. Columbian ground squirrels appear to act as income breeders that also rely on stored capital to increase their propensity for future reproduction. Failed breeders in one year “prepare” for future reproduction by accumulating additional mass, which is “carried over” to the subsequent reproductive season.     

Reproductive performance of little penguins Eudyptula minor in relation to year, age, pair-bond duration, breeding date and individual quality

We measured breeding performance of little penguins Eudyptula minor at Phillip Island, Victoria, Australia, during a 21-year period. All birds considered in this paper (n=307) were of known age (2–22 y) and sex, and most were of known, or closely-estimated, pair-bond status (1–8 mates per bird; pair-bond durations 1–13 y). Breeding dates and breeding performance varied markedly from year to year; measures of annual performance were not associated with early breeding. Measures of individual breeding performance (clutch-size, hatching success, chick masses and productivity) were related to early laying, parental age, and duration of pair-bond. Dependence of breeding performance on parental age was curvilinear, levelling off at about 8 y of age. Productivity declined significantly among birds older than 8 y; this decline was not due to events in the last year of breeding ("terminal illness"). Breeding performance increased with duration of pair-bond at least through y 5. Early breeding was significantly related to age and duration of pair-bond. Most of these relationships were stronger among males than among females, and many of them were not significant when females were considered alone. After controlling for other factors, breeding performance varied significantly among birds, but autocorrelations were low and limited to intervals of one year. Parental quality (defined for birds studied in six or more years as the individual bird term in a GLM for productivity controlling for other factors) was not correlated with lifespan or other demographic parameters, but high-quality birds were less prone to change mates and burrows than low-quality birds. We know of no previous study in which simultaneous effects of laying date, age and pair-bond duration on breeding performance were measured, while controlling for year, individual quality and terminal illness.     

Climate and demography of the planktivorous Cassin's auklet Ptychoramphus aleuticus off northern California: implications for population change

1. We performed demographic analyses on Cassin's auklet Ptychoramphus aleuticus, a zooplanktivorous seabird inhabiting the variable California Current System, to understand how temporal environmental variability influences population dynamics. 2. We used capture-recapture data from 1986 to 2002 to rank models of interannual variation in survival, breeding propensity, breeding success, and recruitment. 3. All demographic parameters exhibited temporal variability. Interannual variation in survival was best modelled as a nonlinear function of the winter Southern Oscillation Index (SOI). Breeding propensity was best modelled as a threshold function of local sea surface temperature. Breeding success and recruitment were best modelled with year-dependent annual variation. 4. Changes in the SOI force El Ni?o/La Ni?a events, which in turn alter prey availability to seabirds in this system. Demographic responses varied during El Ni?os/La Ni?as. Survival diminished substantially during the 1997-98 El Ni?o event, while breeding propensity was affected during both the 1992 and 1998 El Ni?os. Breeding success was reduced during the 1992, 1993, and 1998 El Ni?os, but was unusually high in 2002. Recruitment was higher at the beginning and end of this time-series. 5. While demographic responses varied interannually, parameter values covaried in a positive fashion, a situation conducive to rapid population change. During the 11 years study period, the Farallon auklet breeding population declined at 6.05 +/- 0.80% (SE) per year, a cumulative decline of 49.7%. This study demonstrates how climate variability has influenced key demographic processes for this diminished marine bird population.     

Influence of helping and breeding experience on reproductive performance in the Seychelles warbler: a translocation experiment

Reproductive success of the cooperative breeding Seychelleswarbler (Acrocephalus sechellensis) increases with age. Thisage effect is not due to differential survival or increasedreproductive effort, but to accumulated helping and breedingexperience. In their first year of breeding, reproductive performanceof inexperienced warblers with neither helping nor breedingexperience was significandy lower than that of warblers of thesame age with either previous helping or breeding experience.Reproductive performance was the same for primiparae with helpingexperience and for birds with breeding experience. Female primiparaewith helping experience or breeding experience built betternests and spent more time incubating than inexperienced females,which led to increased hatching success. Male primiparae withhelping experience or males with breeding experience guardedthe clutch better than inexperienced males, which led to reducedegg predation. Even-aged warblers with different previous experienceswere transferred to unoccupied islands, where birds startedbreeding immediately in high-quality territories. The experimentshowed that birds with helping experience produced their firstfledgling as fast as experienced breeders, and significandyfaster than inexperienced birds. Breeding performance did notimprove further with experience after the first successful breedingattempt. Only birds with previous breeding experience who pairedwith inexperienced birds, were likely to change mate. The otherpair combinations remained stable. Thus, primiparous birds withhelping experience have greater lifetime reproductive successthan inexperienced primiparae of the same age. This experimentshows that helping behavior has not only been selected for inthe context of promoting an individual's indirect fitness, butalso in the context of gaining helping experience which translatesinto improved reproductive success when a helper becomes a breeder.[Behav Ecol 7: 326-333 (1996)]     

Breeding site fidelity and natal philopatry in the Redshank Tringa totanus

This paper presents the results of a study carried out on breeding Redshank in the Ribble Marshes, Lancashire, England.
Redshank tend to return to the same breeding area year after year. There was no detectable sex bias in return rates. Experienced birds were more site faithful than inexperienced birds, with previously successful birds exhibiting the highest degree of breeding site fidelity. Older, more experienced birds were more successful at hatching eggs than inexperienced birds.
Breeding dispersal was the same both within and between years. Faithful pairs and males nesting with a new mate dispersed significantly shorter distances than females nesting with a new partner. Dispersal distances in female Redshank were affected by breeding success: unsuccessful females, nesting with a new mate, dispersed significantly farther than successful females. A pair's breeding success influenced the following year's mate fidelity. However, other factors such as overwintering survival and date of return may also have influenced mate fidelity.
Redshank were highly faithful to their natal area; a high proportion of birds that survived post-fledging mortality returned to breed in their area of birth. No sex bias in natal dispersal was detected. Approximately 50% of Redshank breed in their first year of life.     

Habitat selection by dispersing yellow-headed blackbirds: evidence of prospecting and the use of public information

In migratory birds individuals may prospect for potential breeding sites months before they attempt to breed and should use the cues most predictive of future reproductive success when selecting a breeding site. However, what cues individuals use when prospecting and which cues are used in selecting a breeding site are unknown for most species. I investigated whether yellow-headed blackbirds (Xanthocephalus xanthocephalus) prospect for future breeding sites and whether they select breeding habitats based on food availability, male or female density, or the average number of young produced per female in the previous year. Although it is often assumed that migratory birds prospect for potential breeding sites at the end of the breeding season, I investigated this by recording all visits to sites early and late in the breeding season. I found that males and females who visited sites other than the site at which they bred were more likely to disperse than individuals only observed at the site where they bred, and that males and females were more likely to prospect late in the breeding season. Both food availability and density in year ^x were not predictive of the number of young per female in year ^x+1; however, the number of young produced per female at a site in year ^x was predictive of the number of young per female in year ^x+1. As expected, dispersers used the most informative cue, the number of young per female and moved to sites with a relatively high number of young per female. This study suggests that individuals prospect for potential breeding sites late in the breeding season when they can use information gathered from the reproductive success of other individuals (i.e., public information) to select a breeding site.     

Identification and breeding of yearling Piping Plovers

ABSTRACT Age of first breeding is an important life history trait. Many Piping Plovers (Charadrius melodus) do not breed as yearlings, but little information is available concerning the age of first breeding. From 2000 to 2006, we marked 991 chicks in three areas in Saskatchewan, Canada, and subsequently determined when 102 (49 females and 53 males) first bred. Females bred significantly earlier, on average, than males. More females (68%) bred as yearlings than did males (41%; P= 0.04), with most others first nesting when 2‐yr old (29% of females and 50% of males). As expected from differences between the sexes in age of first breeding, younger females were more likely to pair with older males than were younger males with older females. Chicks that hatched early in the breeding season did not breed at an earlier age than those that hatched late in the year. Unlike older birds, juvenile Piping Plovers do not replace flight feathers during their first winter. As a result, 18 of 27 yearlings (67%) had worn outer primaries, whereas only one of 123 (1%) older birds had worn primaries. In addition, whereas 20 of 24 yearlings (83%) retained a few buff‐tipped median coverts, none of 119 known older birds had such coverts. As a result, we were able to identify all yearlings by their worn primaries, buff‐tipped median wing coverts, or both. Wing lengths of yearling Piping Plovers were 3% shorter than those of older birds, presumably due to wear. Because there is no evidence of differences in adult survival rates between the sexes and breeding habitat is available, we speculate that fewer yearling males than females breed because primary wear may reduce the ability of yearling males to perform aerial breeding displays.