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.     

Senescence and carryover effects of reproductive performance influence migration,condition, and breeding propensity in a small shorebird

Breeding propensity, the probability that an animal will attempt to breed each year, is perhaps the least understood demographic process influencing annual fecundity. Breeding propensity is ecologically complex, as associations among a variety of intrinsic and extrinsic factors may interact to affect an animal's breeding decisions. Individuals that opt not to breed can be more difficult to detect than breeders, which can (1) lead to difficulty in estimation of breeding propensity, and (2) bias other demographic parameters. We studied the effects of sex, age, and population reproductive success on the survival and breeding propensity of a migratory shorebird, the piping plover (Charadrius melodus ), nesting on the Missouri River. We used a robust design Barker model to estimate true survival and breeding propensity and found survival decreased as birds aged and did so more quickly for males than females. Monthly survival during the breeding season was lower than during migration or the nonbreeding season. Males were less likely to skip breeding (range: 1–17%) than females (range: 3–26%; β_sex = ?0.21, 95% CI: ?0.38 to ?0.21), and both sexes were less likely to return to the breeding grounds following a year of high reproductive success. Birds that returned in a year following relatively high population‐wide reproductive output were in poorer condition than following a year with lower reproductive output. Younger adult birds and females were more likely to migrate from the breeding area earlier than older birds and males; however, all birds stayed on the breeding grounds longer when nest survival was low, presumably because of renesting attempts. Piping plovers used a variety of environmental and demographic cues to inform their reproduction, employing strategies that could maximize fitness on average. Our results support the “disposable soma” theory of aging and follow with predictions from life history theory, exhibiting the intimate connections among the core ecological concepts of senescence, carryover effects, and life history.     

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.     

THE WINTERING AND MOULT OF RUFFS PHILOMACHUS PUGNAX IN THE KENYAN RIFT VALLEY

Some 5700 Ruffs were ringed in the southern Kenyan rift valley during 1967–79, mainly at Lakes Nakuru and Magadi. These have produced 15 recoveries outside East Africa, 14 in Siberia between 73° and 154°E and one in India. Adult males returned to Kenya mainly during August, and females during late August and early September. Females greatly outnumbered males at all times. Most wintering males departed late in March and early in April, but females not until about a month later. First-year birds appeared from the end of August, but remained in low numbers until late October or November. Most departed during April and May, but a few females oversummered. First-year birds typically accounted for about 25% of the wintering Nakuru females, but about 50% of those at Magadi. At both sites they accounted for a higher proportion of male birds than females. Most of the birds at Nakuru throughout late August to May appeared to be local winterers, and many individuals remained in the area for many months each year. Retrapping indicated that approximately 60% of each season's birds returned the following season. Adult males and most adult females commenced pre-winter wing moult before arrival, but completed most of it in Kenya. Males moulted 3–4 weeks ahead of females, and most had finished before December. Females typically finished during December and early January. Most second year birds timed their pre-winter moult similarly to older adults. Suspension was recorded in over 15% of all moulting birds examined. Adult pre-summer moult involved most or all of the tertials, some or all of the tail feathers, most of the inner wing coverts and the body and head plumage. It occurred mainly during January to March (males) or February to April (females), although tertial renewal commonly began a month earlier. Males showed no sign in Kenya of the supplementary prenuptial moult. First-year birds moulted from juvenile into first winter body plumage during late September to November. They underwent a pre-summer moult similar in extent and timing to that of adults, and again about a month earlier in males than females. Spring feathers acquired were often as brightly coloured as those of adults. About 15% of first-year birds renewed their outer 2–4 pairs of large primaries during January to April. Adult and first-year birds fattened before spring departure, commonly reaching weights 30–60% above winter mean. Weights of adult males peaked early in April, those of adult females early in May, and those of first-winter females later in May. Weights were relatively high also during August and September. This was due to the arrival of wintering birds carrying ‘spare’ reserves, and also apparently to the presence of a late moulting fattening passage contingent. The wing length of newly moulted adults was about 3 mm longer than that of newly arrived first-year birds, but there was no evidence of an increase in the wing kngth of adults with successive moults. Adult wing length decreased by 4–5 mm between the completion of one moult and the middle stages of the next. The migrations and annual timetable of Kenyan wintering Ruffs are discussed, and their moult strategy is compared with that of other Holarctic waders.     

Population structure,biometrics and moult of migrant Purple Sandpipers Calidris maritima in southwest Iceland in spring

Capsule Iceland is a stop‐over site for a population of Purple Sandpipers that winter in Britain. Here, they accumulate fuel loads for onward migration along with birds that have wintered in Iceland.

Aims To establish whether Purple Sandpipers from Britain stop‐over in Iceland during spring migration and, if so, to describe their population structure, changes in mass and moult.

Methods Purple Sandpipers were cannon‐netted on the coast of the Reykjanes Peninsula in southwest Iceland during May 2003 and 2005. Birds were aged, sexed (some by DNA) and standard biometric measurements made. Active body moult was scored.

Results Bill and wing lengths showed that the Purple Sandpipers we caught were similar to one of the populations that winter in Britain rather than Icelandic breeding birds. There were more males than females throughout the migration period (63% males for first‐year‐birds and 67% for adult birds). Accounting for a bias due to a higher percentage of males in a less usual habitat (muddy/sandy bays), the values for rocky sites were 52% males for first‐year birds and 62% for adults. The percentage of first‐year birds was 19% in 2003 and 32% in 2005, though the latter figure was biased by catches in muddy/sandy bays where there was a higher percentage of young birds. The percentage of first‐year birds was 25% on just the rocky shores in 2005. Many birds were in latter stages of body moult, and males were slightly in advance of females. Increasing mass showed that they were preparing for onward migration. The average increase of 0.58 g per day was similar to the rate measured in Orkney at an earlier point on the migration route. However, a high turnover of birds could be the reason for these low values. By late May, and close to the assumed departure date, the Purple Sandpipers of the different age/sex classes had fuel indices of 24–29% (33–42% of the lean mass). This was lower than that for the high Arctic sandpipers (Knots and Sanderlings) leaving southwest Iceland for Greenland and Canada.

Conclusions Our study confirmed that Purple Sandpipers do stop‐over in Iceland, and the possible lower rate of fuel accumulation and smaller amount stored, compared with Knots and Sanderlings, suggests a different migration pattern.     

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.     

Male colour variation in Spanish Pied Flycatchers Ficedula hypoleuca

Male variation in dorsal plumage colour was studied in a montane Spanish population of Pied Flycatchers Ficedula hypoleuca. Adult and yearling males did not differ in colour as measured by Drost's colour types. However, adult males differed from yearlings in being more likely to die if they were light-coloured the year before. Following the same individual males across years yielded a trend towards adult males becoming browner the following year, while no significant differences were found in first-year males. For surviving individual males, becoming browner between successive breeding seasons was associated with relative delays in breeding phenology. Significant but not very high repeatability of male colour is found, and this trait may be subjected to moderate environmental variation, perhaps while moulting in the winter quarters. Overall, being browner may be a sign of ageing and/or poor condition in Spanish Pied Flycatchers.     

Adult survival and numbers in a coastal breeding population of Redshank Tringa totanus in northwest England

The results of a long-term capture-mark-recapture ringing programme carried out on a coastal population of breeding Redshanks Tringa totanus between 1974 and 1988 are presented.
Both sexes were equally likely to be recaptured in subsequent years, as were birds captured for the first time compared with those that had been captured previously. Older birds were more frequently recaptured than were young birds. There was no significant difference in male and female adult survival rates, with a mean of 72% of females and 75% of males surviving each year.
The breeding population fluctuated annually with estimated breeding densities of 122–285 pairs per km². Variation in breeding numbers (males), but not survival, was partially attributable to winter air temperature.     

DISPERSION, POPULATION ECOLOGY AND MIGRATION OF EASTERN GREAT REED WARBLERS ACROCEPHALUS ORIENTALIS WINTERING IN MALAYSIA

A population of 400–600 Acrocephalus orientalis wintering in a Phragmites habitat at 3°N in West Malaysia was studied during four northern hemisphere winters, by means of systematic mist-netting. Data from other study-areas, other habitats and other winters are also used. Intensive mist-netting appears to have made birds move over longer distances than they did in the absence of disturbance, and to have led to the emigration of marked birds from the study-area. Trapping also affected feeding behaviour, resulting in weight-loss; repeated trapping may have increased mortality. Males and females could be separated by means of wing-length in fresh plumage. Females were largely confined to Phragmites; males were more numerous on the edge of reed-beds and in scrub vegetation. Males suffered greater feather-wear than females. As measured by the trapping rate, birds were uniformly distributed throughout the Phragmites habitat, at the same density in different winters. Undisturbed birds used a “home-range” of 1–4 ha, overlapping with 15–50 other individuals. Disturbed birds overlapped with 100–200 others. Individual birds returned to exactly the same “home-range” in successive winters. After correcting for the effects of disturbance and incomplete sampling, the proportion of adults ringed in one winter which returned in the next is estimated as 65% in each of two study-areas. This is a minimum estimate of the annual survival rate for adults. Mean total body-weights were at a minimum in midwinter (November-February). Fat-free weights were also lower in midwinter than in autumn and spring. Body-moult was observed in March and April. Moult of the flight-feathers takes place between July and September, on the breeding grounds or slightly to the south. Females departed on spring migration between 10 and 25 May; males some 11–14 days earlier. Adults arrived in autumn between 8 September and 7 October; males and females often came in in separate “waves”. Females were absent for only about 127 days, about the minimum required for migration, breeding and moult. Dates of migration match those of the more northern breeding populations. Spring departure is later than dates of passage recorded in south China; hence birds of this population appear to make long nights. On average, birds departing in spring carried about 9 g of fat, roughly 40% of total fat-free body-weight. This is about half the energy reserve required for the entire journey. Dates of passage in central China are consistent with a hypothesis that they make the journey (4,500-5,000 km) in two “hops”. A few birds which remained light until very late in the spring showed a significantly lower return rate in the next year. Most birds arriving in autumn appear to have carried 1–2 g of fat, but some were at or below the normal fat-free weight. Many birds appear to have lost weight soon after arrival. Returning ringed adults were amongst the very first birds trapped in September. Individual birds appear to have migrated on very similar dates in different years: many of the dates of trapping differed by 2 days or less in successive years. Trapping rates reached a peak in early October and then declined rapidly, reaching the midwinter level by 21 October. The decline coincided with the differential disappearance of juvenile birds. However, birds collected at this time had adequate fat reserves, and the disappearance appears to have preceded the period of food-shortage. It is suggested that the loss of juvenile birds resulted from behavioural interactions favouring the more dominant individuals, as has been described for several temperate zone residents. The first few weeks in the wintering area may thus be the critical period of mortality during the year. Because birds from different breeding areas are expected to be mixed in the winter-quarters, and vice versa, local mortality factors in winter may affect a number of breeding populations. High adult survival rates have been recorded in several other birds which breed in the temperate zones and winter in the tropics. In general their breeding success appears to be high, so the first-year mortality must be high. The closely related A. arundinaceus, which winters in Africa, differs from A. orientalis in size, wing-shape, timing of spring migration and timing of moult. These differences can be interpreted as adaptations to different environmental (primarily climatic) factors experienced during migration and on the breeding grounds. The segregation of males and females into different habitats probably reduces inter-sexual competition in winter, but this is not necessarily its primary function. Males collected in the evening in Phragmites had smaller fat reserves than females, suggesting that the females are better adapted to this habitat. The large size of the males is probably maintained in part by sexual selection in the breeding season. On the other hand, the size of females and their habitat is probably limited by the specialisation of their nest. These factors would suffice to explain the sexual dimorphism in size and habitat.     

Reconnaissance for future breeding sites by spotted sandpipers

We studied the sex-role-reversed, polyandrous spotted sandpiper(Actitis macularia) from 1974 to 1990 in northern Minnesota,USA. After peak arrival of breeding birds and before peak departureat the end of the breeding season, there were many short-termvisitors (transients) to the study site. Stepwise discriminantfunction analysis (DFA) was used to determine the importanceof absolute sex ratio (males/female), sex of the transient bird,number of nests, and number of breeding males and females duringthe week of visit in predicting whether a visiting bird wouldreturn the following year. In addition, multiple regressionwas used to determine how much variability in the number oftransient birds returning in subsequent yearscould be explainedby annual values during the year of transience for numbers ofbreeding males and females, numbers of eggs laid and hatched,and absolute sex ratio. Annual recruitment of foreign adultsranged from 1 to 20 birds, of which 0–56% were seen visitingin previous years. Female recruits were more likely than malesto have been observed previously as transients. Twenty-two chickshatched at our study site returned and bred for the first timemore than 1 year after hatching. Of these, 9 (41%) were seenas transients between the year of hatch and breeding. The DFAshowed that transient females returned more often than transientmales and that the number of transients returning in subsequentyears was positively associated with the absolute sex ratioduring the week visited. When the sexes were analyzed separately,none of the weekly variables significantly discriminated femalereturn, but sex ratio was positively associated with male return.Regression showed that the number of transient birds returningin subsequent years was positively associated with the numberof male breeders at our study site during the year a bird visited.Percentage return the year after transience was positively associatedwith the number of eggs laid at our study site during the yeara bird visited. When sexes were analyzed separately, the higherthe number of female breeders during the year a bird visited,the greater the number of males returning in subsequent years,and greater numbers of breeding males were positively associatedwith transient female return. Based on our results, we suggestthat transient birds were searching for better breeding areasfor future breeding and that intrasexual competition made thisinformation more important to females than to males.     

Temporal variation of juvenile survival in a long-lived species: the role of parasites and body condition

Studies of population dynamics of long-lived species have generally focused on adult survival because population growth should be most sensitive to this parameter. However, actual variations in population size can often be driven by other demographic parameters, such as juvenile survival, when they show high temporal variability. We used capture–recapture data from a long-term study of a hunted, migratory species, the greater snow goose (Chen caerulescens atlantica), to assess temporal variability in first-year survival and the relative importance of natural and hunting mortality. We also conducted a parasite-removal experiment to determine the effect of internal parasites and body condition on temporal variation in juvenile survival. We found that juvenile survival showed a higher temporal variability than adult survival and that natural mortality was more important than hunting mortality, unlike in adults. Parasite removal increased first-year survival and reduced its annual variability in females only. Body condition at fledging was also positively correlated with first-year survival in treated females. With reduced parasite load, females, which are thought to invest more in their immune system than males according to Bateman’s principle, could probably reallocate more energy to growth than males, leading to a higher survival. Treated birds also had a higher survival than control ones during their second year, suggesting a developmental effect that manifested later in life. Our study shows that natural factors such as internal parasites may be a major source of variation in juvenile survival of a long-lived, migratory bird, which has implications for its population dynamics.     

Breeding site fidelity in willow ptarmigan: the influence of previous reproductive success and familiarity with partner and territory

Summary Breeding site fidelity is high in willow ptarmigan: only 9% of males and 31% of females switched territories between years. Unpaired males were more likely to switch territories than paired males. For paired males, survival of their previous partner and reproductive success in year x did not influence probability of switching in year x+1. A female was more likely to switch territories if her previous partner disappeared. If her partner returned, she had a higher probability of switching if she did not produce chicks the previous year. Most hens moved to the territories of older males, although hens paired with unfamiliar older males did not have higher reproductive success than those paired with yearlings. Individuals that paired with their previous partner laid earlier and produced heavier chicks than those paired with unfamiliar partners. Excluding birds paired with familiar partners, survival and reproductive success in year x+1 was similar for males and females that did or did not switch territories. Males had a higher probability of producing chicks after switching than before, but females were more likely to lose their clutch after switching. For both sexes, birds that switched territories were as successful as the birds that replaced them on their former territories. We conclude that high site fidelity in willow ptarmigan is maintained because of the benefits of pairing with a familiar partner.     

WINTER SURVIVAL IN RELATION TO DOMINANCE CLASSES AMONG SILVEREYES ZOSTEROPS LATERALIS CHLOROCEPHALA OF HERON ISLAND, GREAT BARRIER REEF

Winter survival with respect to dominance classes of 932 individually colour-ringed Silvereyes was examined on Heron Island, Great Barrier Reef, between 1965 and 1969. The dominants (winning two-thirds or more of aggressive encounters) had significantly better chances of survival between May and August (southern winter) than other birds. The 1967/68 year group was studied in detail; the young born early in the breeding season contained proportionately more dominants than those born later in the season and dominant birds tended to survive better in winter. Adults in the same period showed no dominance dependent survival. The weight of birds in winter differed between first-year birds and adults in most cases, but winter mortality within each year-group was not related to the weight of individual birds in May. However, the dominant class had a smaller proportion of birds losing weight through the winter than other classes, and the dominant adults and the intermediate class of first-year birds tended to be heavier than others in August. The lengths of wing, tail, tarsus and exposed culmen examined for the 1967/68 year group showed no significant trends in either survival or dominance classes. Better survival of dominant birds is considered to be a consequence of their feeding advantages over others, but the intensity of selection for an ability for dominance may fluctuate from year to year in relation to the population density and distribution and abundance of food supply.     

Turnover and dispersal in a Peregrine Falco peregrinus population

In south Scotland, most Peregrines returned to the same territories to breed in successive years, though a few females changed territory from one year to the next.
Annual mortality among breeding birds was at most 9% among females (or 11% in both sexes combined). There may have been considerable annual variation, however, and excluding one exceptional year out of five reduced the estimate for females to 7%. These estimates are maxima, but are still considerably lower than those obtained from ring recoveries of dead birds reported by members of the public.
Among trapped birds, four males first bred at age two years, one at three and another at four or five; two females first bred at one year, 13 at two years old and one at three. Five other females which were seen to be in first-year plumage but were not trapped, also laid eggs, and 12 other such paired females held territory but did not lay. Only one paired male held territory in first-year plumage.
In their movements between natal and breeding territories, some females moved further than males, with median distances of 83 and 58 km respectively. In addition, of birds trapped breeding in the study area, a greater proportion of the males than of the females had been born locally, despite an equal sex ratio among fledglings; this was also consistent with a greater dispersal of females. In general, Peregrines made much longer movements in their first year of life than subsequently. Movements were in any direction.     

Increased extra‐pair paternity in broods of aging males and enhanced recruitment of extra‐pair young in a migratory bird

Despite keen interest in extra‐pair mating in birds, its adaptive significance remains unresolved. Here, we use a multi‐year dataset to test whether traits of a female's social mate influence her propensity to produce extra‐pair offspring in a population of house wrens, and whether producing extra‐pair young has consequences for a female's fitness through effects on offspring survival. Females were most likely to produce extra‐pair offspring when paired with old males and when paired with males on poor‐quality territories, although this latter effect was marginally nonsignificant. Among offspring, the cutaneous immunity of within‐pair young decreased as the age of their sires increased, but cutaneous immunity of extra‐pair young was not affected by the age of their extra‐pair sires or by the age of the males rearing them. Extra‐pair offspring were more likely than within‐pair offspring to return as breeding adults to the local population, with extra‐pair sons being more likely to return as a breeder for multiple years. Our findings support the hypothesis that females produce extra‐pair offspring to enhance their inclusive fitness beyond what they are capable of given the male with which they are socially paired.     

Family-based winter territoriality in western bluebirds, Sialia mexicana: the structure and dynamics of winter groups

Winter residency is characteristic of the majority of cooperatively breeding birds, but the composition and dynamics of winter groups have been examined in relatively few. In 1996-1998, we examined winter territoriality in the western bluebird, a year-round resident that shows a limited degree of helping behaviour in central coastal California, U.S.A. In spring, most western bluebirds breed as socially monogamous pairs, but a small proportion of pairs (3-16%) have additional breeding-age males helping at the nest, usually assisting parents or brothers. We found that year-round residents commonly wintered in family groups that defended territories similar to those used in spring. Winter groups had an even sex ratio and formed early in the autumn, when hatch-year birds dispersed. More females than males left their natal groups to be replaced by an influx of immigrant hatch-year birds. Winter groups typically consisted of breeders and one or two sons from the prior breeding season along with one or more immigrant females. A second period of dispersal occurred in spring when winter groups broke up and most birds other than the breeding pair left the winter territory. When they bred, yearling males and females often bred with unrelated individuals from their winter groups. Sons were more likely to remain on the study area as yearlings when they wintered with both parents than when they wintered with just one parent. We suggest that young males stay the winter due to benefits of remaining in family groups on mistletoe-based winter territories. Subsequent localized dispersal of sons then leads to opportunistic kin-based interactions later in life. Copyright 2001 The Association for the Study of Animal Behaviour.     

Winter survival and breeding success of dominant and subordinate Willow Tits Parus montanus

We studied the effect of winter rank on survival rate and reproductive success in Willow Tits Parus montanus, a resident passerine living in dominance-structured flocks during the nonbreeding season, in 6 years. Winter survival was dependent on both the birds' age and rank. Adults survived better than first-year birds, and within first-year males, dominants survived better than subordinates. In other sex and age classes, rank did not contribute to survival. Although first-year males were in excess among nonbreeders, no connection existed between breeding status and rank. Female rank did not explain the variation in the start of laying, clutch size, number of fledglings or recruit production. We conclude that social status in Willow Tits affects individual fitness mainly through rank-dependent survival. Acquiring a high rank position seems to be most important for first-year birds, especially first-year males.     

Sea buckthorn berries Hippophae rhamnoides L. predict size and composition of a great tit population Parus major L

In seasonal environments variation in food abundance in the non‐breeding season is thought to affect songbird population dynamics. In a unique tit‐sea buckthorn berry system we can estimate the berry abundance and both the tit consumption and population dynamics. Six hundred nest boxes were available to great and blue tits Cyanistes caeruleus for breeding in spring and roosting in winter. We followed the dynamics including the recapture histories of individually marked great tits from 2008 to 2014. In each year we estimated 1) the winter sea buckthorn berry availability, 2) an index of berry consumption in December based on the colour of the faeces of roosting birds, 3) the number of breeding great and blue tits, 4) both recapture probability and the return rate of the great tits and 5) immigration rates. December berry abundance positively predicted the number of breeding pairs of both species in the subsequent season and great tit return rates in the second half of the winter. There was support for a sex specific berry effect on the adult return rate in the great tit: female return rate was associated less strongly to berry abundance than male return rate. This skewed the sex ratio of the local breeders in the following breeding season. Intriguingly, annual berry consumption in December was not related to berry abundance, and individuals consuming more berries tended to have slightly lower return rates. Reproductive rate was not related to berry abundance. There was hardly support for a relation between immigration rates of first year breeders and berry abundance. Taken together these results imply that berry stock not only affected population size but also the population composition through sex specific exchange with the surroundings. Since population density covaried with berry abundance, density dependent effects provide an alternative explanation for the patterns observed.     

Cold tolerance,and not earlier arrival on breeding grounds,explains why males winter further north in an Arctic‐breeding songbird

Sex biases in distributions of migratory birds during the non‐breeding season are widespread; however, the proximate mechanisms contributing to broad‐scale sex‐ratio variation are not well understood. We analyzed a long‐term winter‐banding dataset in combination with spring migration data from individuals tracked by using geolocators to test three hypotheses for observed variation in sex‐ratios in wintering flocks of snow buntings Plectrophenax nivalis. We quantified relevant weather conditions in winter (temperature, snowfall and snow depth) at each banding site each year and measured body size and condition (fat scores) of individual birds (n > 5500). We also directly measured spring migration distance for 17 individuals by using light‐level geolocators. If the distribution pattern of birds in winter is related to interactions between individual body size and thermoregulation, then larger bodied birds (males) should be found in colder sites (body size hypothesis). Males may also winter closer to breeding grounds to reduce migration distance for early arrival at breeding sites (arrival timing hypothesis). Finally, males may be socially dominant over females, and thus exclude females from high‐quality wintering sites (social dominance hypothesis). We found support for the body size hypothesis, in that colder and snowier weather predicted both larger body size and higher proportions of males banded. Direct tracking revealed that males did not winter significantly closer to their breeding site, despite being slightly further north on average than females from the same breeding population. We found some evidence for social dominance, in that females tended to carry more fat than males, potentially indicating lower habitat quality for females. Global climatic warming may reduce temperature constraints on females and smaller‐bodied males, resulting in broad‐scale changes in distributional patterns. Whether this has repercussions for individual fitness, and therefore population demography, is an important area of future research.     

The reproductive ecology of resident manta rays (Manta alfredi) off Maui, Hawaii, with an emphasis on body size

In resident manta rays (Manta alfredi) off Maui, sexual maturity appears delayed until growth exceeds 90% of maximum size, an indicator that large body size provides a reproductive advantage at the expense of a shorter reproductive time period. In this study, 286 surveys were conducted between 2005 and 2010 using photo-identification and photogrammetry to study the reproductive ecology of a resident population of manta rays off Maui, Hawaii, and investigate the reproductive benefits of large body size in each sex. Although reproductive activities occurred year-round, mating trains and late-term pregnant females were significantly more likely to be observed during the winter months. Some females were pursued by males during both winter and summer of the same year, suggesting multiple ovulations may be possible in a single year. Males likely detect a female’s reproductive state by positioning directly behind her, or passing through her bodily excretions. The mean pregnancy rate was estimated at 0.56 pregnancies/adult female/year with larger females pregnant more often, and more likely in consecutive years. The operational sex ratio was heavily skewed with 2.68 adult males per reproductively available female. Although males appear to compete with one another for females within a mating train, no direct physical competition was ever observed between males. Evidence of highly dynamic mating trains lasting more than one day suggests endurance rivalry may be the primary mating strategy among males, during which larger males may benefit from greater energy reserves. The study area appears to be an important staging area for mating individuals in this population.