THE EFFECT OF AGE ON THE BREEDING BIOLOGY OF THE KITTTWAKE RISSA TRIDACTYLA

1. From 1954 to 1956 inclusive, the biology of individual marked Kittiwakes was studied at North Shields, Northumberland.
2. It was concluded that older Kittiwakes reacted to the breeding stimulus earlier, more intensively and with greater success than younger breeding birds.
3. Birds with previous breeding experience returned to the colony before birds breeding for the first time and these before non-breeders.
4. Before breeding started, birds which had bred previously spent more of their time at the colony than those about to breed for the first time.
5. Birds breeding for at least the second time laid the first egg 7·5 days earlier than those breeding for the first time.
6. Breeding started one day later for every four days the return to the colony was postponed.
7. Older breeding birds showed greater nest-site tenacity, laid larger clutches and had greater breeding success than younger birds.
8. The chicks in broods of two (but not of one) increased in weight more rapidly where the parents had previous experience.
9. Breeding Kittiwakes showed strong colony tenacity, but 24% of the marked non-breeding birds were subsequently seen in other colonies.
10. Over half the birds retained the same mate as in the previous year.     

Pair bond and breeding success in Blue Tits Parus caeruleus and Great Tits Parus major

Data from 939 nests of the Blue Tit Parus caeruleus and 1008 nests of the Great Tit P. major from nestboxes provided in superabundance in mixed forest study sites between 1976 and 2001 were analysed to examine the effects of mate retention on breeding success and the relationship between mate fidelity and site fidelity. Most birds retained their former partner (76% in Great Tits and 65% in Blue Tits). The probability of a pair divorcing was affected by male age in Great Tits, divorce being more likely in pairs with first‐year males. Great Tit pairs breeding together for a second season bred earlier, but had no higher breeding success than pairs breeding together for the first time. In Blue Tits laying date and start of incubation tended to be earlier in pairs breeding together for a second season, but hatching and fledging dates were not earlier than in other pairs. Great Tit pairs breeding together for two consecutive seasons bred earlier in the second season than in the first, but breeding success did not differ significantly between years. In both species, breeding performance did not differ between pairs that divorced after a season and pairs that stayed together. Thus breeding success did not determine whether a pair divorced or bred together again. Neither Blue Tits nor Great Tits improved their breeding performance through divorce. Blue Tit females even had fewer fledglings in the year after divorce than in the year before. Mate retention affected breeding site fidelity. Blue Tit females had greater breeding dispersal distances between consecutive years when re‐mating than when breeding again with the same mate. In Great Tits both males and females dispersed more when re‐mating than when retaining the former partner, suggesting that mate retention increased the chance of retaining the breeding site. In both species, breeding dispersal distances did not differ between pairs that divorced and pairs in which one mate disappeared. Because no major advantage of mate retention was evident, we suggest that mate retention evolved under different conditions than those found in study sites with high breeding densities and a superabundance of artificial nesting sites.     

ATTENDANCE PATTERNS OF CALIFORNIA SEA LION (ZALOPHUS CALIFORNIANUS) FEMALES AND PUPS DURING THE NON-BREEDING SEASON AT SAN MIGUEL ISLAND

The attendance patterns of California sea lions were studied during the non-breeding seasons from 1991 to 1994. Lactating females frequented the rookery to nurse their pups until weaning; most non-lactating females left the rookery for the season. Females spent over 70% of their time at sea except in 1993 when they spent 59% of their time at sea. The mean foraging trip length in the winter and spring ranged from 3.3 to 4.6 d; the mean nursing visit ranged from 1.2 to 1.4 d. The duration of foraging trips and nursing visits was variable over the season for individuals but no pattern of change was detected. Interannual and seasonal differences were not significant for time at sea, visits ashore, or foraging-trip duration before, during, or after the 1992-1993 El Niño event. Pups spent an average of 66.6% of their time ashore and up to three days away from the rookery during their mother's absence. Most females and pups stayed associated until April or May. The results suggest that seasonal movement of prey is more important in determining attendance patterns late in the lactation period than increasing energy demands of the pup.     

Is Divorce in Young Common Terns,Sterna hirundo,after Recruitment just a Question of Timing?

The probability of divorce in birds has been linked with age, breeding experience, reproductive output and synchrony in return. Here, we investigate the consequences of first breeding attempts in common terns for mating in the subsequent season. Nearly 20% of all first‐time breeders disappeared or skipped at least one season after recruitment. In 84 pairs, which consisted of at least one recruit and of which both partners returned to the colony, the divorce rate was 45%. We compared reproductive success, arrival dates, and asynchrony in arrival dates of pairs of the first breeding season against the second season, for both reunited and divorced pairs and males and females separately. First, in pairs of which both members came back to the colony, we found an increase of reproductive success most pronounced in males. In the second season reproductive success of divorced compared with reunited pairs was higher, as only divorced pairs significantly improved the number of fledglings, and again this relation was stronger in males. Secondly, females of reunited pairs arrived significantly earlier from the first to the second season and by far more days than their males. However, in divorced pairs former mates did not differ in the number of days they advance their arrivals. Finally, divorced males arrived on average 4 d earlier than their former mates, whereas divorced females arrived 5 d later compared with their former mates of the recruitment season. Contradictory to nearly all other divorce studies in birds so far, we found a clear fitness gain in divorced males. We suggest that the improvement in reproductive success of young males stems from a side‐effect of the birds’ quality and ability to reach the breeding site in appropriate time and earlier as potential competitors. In long‐lived bird species the heterogeneity among young individuals in the timing of arrival at the colony seems to explain why former recruit‐pairs reunite or split. For young males we suggest as best explanation of divorce that they profit from ‘pushing for an empty chair’, while females seem to profit from their choosiness and may actively decide between former and other mates.     

Rhinoceros Auklet pair‐mates migrate independently but synchronize their foraging activity during the pre‐laying period

Pair bonds are considered important for successful breeding in monogamous birds but their maintenance may be challenging for migratory species, as mates can be separated for months during the non‐breeding period. To investigate whether mates of monogamous migratory seabirds stay together throughout the non‐breeding period and how and when they start synchronizing their activity before breeding, we tracked seven pairs and 22 individuals of Rhinoceros Auklets Cerorhinca monocerata with geolocators and saltwater immersion loggers. Mates migrated across similar areas during the non‐breeding period but with a sustained temporal shift, putting them an average of 377 km apart and resulting in an average difference of return date at the colony of 5.6 days, with no sex biases. These values did not differ significantly from those between ‘pairs’ of randomly selected, non‐mated birds. Mates showed synchronized on‐water/in‐air at‐sea activities once both birds returned and spent the first night together at the colony. The synchronization of activities was highest on the day following the nights when both mates visited the colony, and decreased with elapsed time. Mates then left the colony together for a pre‐laying exodus of 8–9 days and males returned 2–4 days earlier than females before incubation started. Mates kept synchronizing at‐sea activity during the early part of the exodus. We interpret this as the mates staying together at sea during the pre‐laying period, increasing the males’ chances of copulation at sea. The patterns of mate association observed in Rhinoceros Auklets contrast with those of the Procellariiformes, presumably reflecting differences in the place and timing of copulation.     

Effects of maternal age and condition on parturition and the perinatal period of Antarctic fur seals

The effect of maternal age and condition on the date of parturition and the duration of the perinatal period of Antarctic fur seals at Bird Island, South Georgia, were investigated over three consecutive breeding seasons. Females rear young during a four-month lactation period in a highly seasonal but predictable environment. Although females may first pup at three years of age, they did not attain full adult size until six years of age; older females (≥ 6 years) tended to be heavier, longer, and in better condition than younger females (3–5 years). Older females returned to breeding beaches earlier and could occupy the most suitable pupping sites, and gave birth when densities of animals on the beaches were low (i.e. more favourable for pup survival). Females that arrived earlier were able to remain ashore longer with their pups prior to departing on their first foraging trips but this was unrelated to either maternal age or condition. Younger females returned later in the pupping season, possibly as a result of late implantation due to smaller energy reserves than older and larger females. In 1990 all females arrived late, were in poorer condition, gave birth to lighter pups, and had shorter perinatal periods. This suggests that not only was implantation late but that females returned to an area of low food availability prior to parturition.     

Age at first breeding, philopatry and breeding site-fidelity in the Lapwing Vanellus vanellus

Breeding Lapwings Vanellus vanellus were studied in the Eden Valley (Cumbria) and in Teesdale (County Durham) between 1990 and 1992. A total of 300 adult Lapwings and 801 near-fledged young were uniquely colour-ringed. Breeding adults were highly site-faithful, almost always nesting in the same or an adjacent field in successive years. Second-year birds were less site-faithful, with more birds nesting in adjacent and other fields and fewer in the same field in successive years. In Teesdale, 74% of colour-ringed young Lapwings returned in their first or second year of life to within 5 km from where they hatched. In contrast, in the Eden Valley only 37% of young birds in their first or second year of life returned to within 5 km from where they hatched. From an analysis of British ringing recoveries in April and May, 61% of Lapwings were recovered within 10 km from where they were ringed as chicks. A further 11% were recovered more than 100 km from where they were ringed. Young Lapwings were highly philopatric, with 45% of males and 52% of females breeding in the same field or a field adjacent to where they hatched. The majority of Lapwings (67%) began breeding at 1 year old. Of the remaining birds, 27% bred for the first time when 2 years old and 6% for the first time in their third year of life. There was no difference between the sexes. Chicks hatching and subsequently fledging late in the season returned less frequently to the study areas in subsequent years than did chicks hatching earlier in the season.     

Sex, age, experience and condition as factors affecting arrival date in prospecting common terns, Sterna hirundo

Several studies have shown that seabird colonies consist to a large extent of young nonbreeders (prospectors). These individuals appear at the colony later in the season than established breeders. The reasons for this late arrival have remained unclear in most cases, mainly because of technical difficulties in collecting sufficient data from nonbreeding individuals. We used a novel transponder system to identify remotely the members of a common tern colony, including nonbreeders, during eight breeding seasons and we combined the system with automatic balances. Ninety-two per cent of prospectors returned for the first time when 2 years old and 88.9% of recruits to the breeding population had spent at least one previous season at the colony as prospectors. In both sexes, most individuals prospected for one season, but more males than females prospected for more than one season, although a higher proportion of females started breeding without a previous prospecting phase. Terns arrived earlier in the season the older they were and the more experience of the colony they had, but experience proved to be more important than age. Prospectors gained about 3 weeks with a previous prospecting season whereas an additional year of age allowed birds to arrive only about 6 days earlier. Prospectors returning later in the season arrived with lower body masses. Males on average arrived earlier at the colony than females. Copyright 2003 Published by Elsevier Science Ltd on behalf of The Association for the Study of Animal Behaviour.      

THE BIOLOGY OF THE WAVED ALBATROSS DIOMEDEA IRRORATA OF HOOD ISLAND, GALAPAGOS

As a nesting species, the Waved Albatross Diomedea irrorata is restricted to Hood Island in the Galapagos archipelago where 12,000 pairs bred in 1971. Outside the islands the species occurs over the northern parts of the Humboldt Current. Two colonies were studied in detail (1970–1971). At the start of a season, males returned first to the colonies and defended a small territory. Copulation occurred without any elaborate ceremony and the female spent little time on land before laying. There was no fixed nest-site, even within a season, and birds moved their eggs considerable distances. This resulted in heavy egg losses. Younger birds bred later than older birds and laid longer but narrower eggs. The average incubation spell varied from four to five days at the extremes of the incubation period to 19 days in the middle. The average incubation and fledging periods were 60 and 167 days respectively. Pairs which lost an egg sometimes adopted the abandoned egg of another bird and successfully reared the chick. Most pairs nested in both seasons. Nesting success was extremely variable, both between years and between colonies. Between 1961 and 1971 at Punta Suarez, virtually no young were reared in four seasons. Even in 1970–71, where nesting success was good, some groups of birds deserted their eggs en masse whereas in neighbouring areas up to 80% of the pairs reared young. The main foods of the young were squid and fish. Birds did not moult wing and tail feathers at the breeding colonies, and about 50% retained some primaries for more than one season, suggesting that successful pairs had difficulty in fitting in a complete moult between breeding attempts. Old feathers were normally found among the inner primaries and at the next moult were preferentially replaced, though adjacent newer feathers were sometimes retained for another season. Some birds bred in their fourth years, but most not until a year or two older. Immatures were present at the colonies late in the breeding cycle, the youngest returning latest and remaining until the last young fledged. Survival of adults and young averaged at least 95% and 93% per annum over many years. Adults and young ringed in 1961 survived equally well. The significance of the timing of the return of immatures and of the large-scale desertion of eggs, apparently not due to food shortage or disturbance, is discussed.     

The long engagement of the emperor penguin

In birds, courtship is generally short relative to the whole breeding cycle. Emperor penguins (Aptenodytes forsteri), however, are an exception as their courtship period is much longer (ca. 6 weeks) than the courtship of other penguin species. This strategy may appear surprising, as it is especially costly to fast and endure drastic climatic conditions for long periods at the colony (1.5 and up to 4 months for females and males, respectively). We examined here the reasons of this extended courtship period and found that emperor penguins returned earlier to the colony when primary oceanic production before breeding was high. This suggests that emperor penguins return to the colony as soon as primary oceanic production in summer allows them to replenish their body reserves. The extended period of time spent at the colony during courtship may therefore result from an evolutionary process that confers advantages to emperor penguins that arrive earlier at the colony by reducing predation risks and offering better chances of securing a partner.     

Dispersion and site fidelity of breeding female grey seals (Halichoerus grypus) on North Rona, Scotland

Female grey seals ( Halichoerus grypus ) formed breeding aggregations on the island of North Rona, Scotland. Aggregations of females were associated particularly with gullies leading from the sea, leaving large areas of available space unoccupied. Changes in the degree of aggregation of females during the breeding season were similar in 1987, 1988 and 1989. Pronounced aggregations occurred in the early and late parts of each breeding season.
Of 67 breeding females marked in 1985, 62 (93%)) returned to N. Rona to breed in at least one season up to 1989, but 18 (27%) were present in all five years. Females came ashore up to 14 days before giving birth and 82% were observed first in the vicinity of their subsequent pupping site. Between 1985 and 1989, marked females which returned were faithful to their previous pupping sites, even when the previous pup had died. There was no evidence of a gradual change in the location of individual pupping sites over time. This pupping site fidelity may generate aggregations whose location, timing and composition is predictable.     

Seasonal sex–specific energy expenditure in breeding and non-breeding Palestine sunbirds Nectarinia osea

The timing of the chick‐rearing phase is known to have a profound effect on the reproductive success of birds. However, little is known about the energetic costs faced by the parents during different periods of the breeding season. These costs may have vital consequences for both their survival and future reproduction. In most studies, daily energy expenditure (DEE) of breeding and non‐breeding birds has been compared, without controlling for the effect of season. In the present study, we examined the energy demands of breeding compared to non‐breeding Palestine sunbirds Nectarinia osea and whether there were sex‐specific differences in DEE within and between different seasons. We predicted that DEE would be elevated when birds rear chicks, especially at cooler ambient temperatures. Time‐energy budgets were constructed for pairs of sunbirds, rearing chicks, or not breeding, in spring and summer. There were significant seasonal differences in estimates of DEE in non‐breeders that were 21% higher in spring than in summer. We attributed these to increases in non‐flight metabolic rate rather than changes in time spent on different activities. Our estimates of DEE for the birds that were rearing chicks were higher than non‐breeding adults. In females the increase in DEE when breeding, compared to when not breeding, was similar in both spring and summer, while males increased their DEE much less when breeding in spring. The differences in estimated DEE, however, were not significant between male and female birds in any season. Between seasons, female breeders had 17.1% higher DEE in spring than in summer, while male breeders showed no difference in DEE when rearing chicks in different seasons. Accordingly, our initial prediction was supported, as DEE in chick‐rearing adults was higher than in non‐breeding adults. In addition, although temperatures are lower in spring, breeding in the spring is only more costly than breeding in summer for females. Apparently, males are more flexible in reallocating their time and energy spent on different activities.     

Biology and survival of the immature Puffin Fratercula arctica

The biology and survival of Puffins were studied in northeast Scotland. Puffins usually bred first when aged four or five years but returned for several seasons prior to this. Young birds were probably prevented from returning earlier in the season because they moult their primaries in the spring and early summer. As they got older, they came to the colony earlier in the year, displayed and tried to get a burrow. Younger immatures may summer in specific areas away from the colonies.
Many immatures visited colonies other than where they were hatched. This was particularly marked in July of their third year. Up to 23% of Puffins of both sexes permanently emigrated and it is suggested that such behaviour is widespread among auks.
About 60 % of fledglings returned to the natal colonies and 30% of fledglings appeared to reach breeding age (although the true figure will be higher as this does not include birds which emigrated). Adult survival was c. 96% per annum. The population could theoretically increase by c. 7% but the observed rate of increase was c. 9% per annum.     

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.     

Sexual,Seasonal and Group Size Differences in the Allocation of Time between Vigilance and Feeding in the Greater Rhea,Rhea americana

We studied the effect of sex and group size on the proportion of time a greater rhea, Rhea americana, allocates to vigilance and feeding during the breeding and the non-breeding seasons. We analysed 175 records of focal animals that were feeding alone or in groups of 2 to 26 birds. In both seasons, males spent more time in vigilance and less time in feeding than females. Both sexes spent more time in vigilance and less time in feeding during the breeding season. Sexual and seasonal differences in vigilance were the result of different mechanisms. Males had shorter feeding bouts than females but there were no sexual differences in the length of the vigilance bouts. On the contrary, seasonal differences were the result of males and females having longer vigilance bouts during the breeding season but there were no seasonal differences in the length of the feeding bouts. During the non-breeding season, individual vigilance was higher in rheas foraging alone than in groups. In this case, solitary birds had longer vigilance and shorter feeding bouts than birds foraging in groups. We discuss the possible effect of intragroup competition and food availability on the allocation of time between feeding and vigilance in this species.     

Novel methods reveal shifts in migration phenology of barn swallows in South Africa

Many migratory bird species, including the barn swallow (Hirundo rustica), have advanced their arrival date at Northern Hemisphere breeding grounds, showing a clear biotic response to recent climate change. Earlier arrival helps maintain their synchrony with earlier springs, but little is known about the associated changes in phenology at their non-breeding grounds. Here, we examine the phenology of barn swallows in South Africa, where a large proportion of the northern European breeding population spends its non-breeding season. Using novel analytical methods based on bird atlas data, we show that swallows first arrive in the northern parts of the country and gradually appear further south. On their north-bound journey, they leave South Africa rapidly, resulting in mean stopover durations of 140 days in the south and 180 days in the north. We found that swallows are now leaving northern parts of South Africa 8 days earlier than they did 20 years ago, and so shortened their stay in areas where they previously stayed the longest. By contrast, they did not shorten their stopover in other parts of South Africa, leading to a more synchronized departure across the country. Departure was related to environmental variability, measured through the Southern Oscillation Index. Our results suggest that these birds gain their extended breeding season in Europe partly by leaving South Africa earlier, and thus add to scarce evidence for phenology shifts in the Southern Hemisphere.     

CHAIRMAN'S REPOST, 1954–55

Brown, C. R. 1986. Feather growth, mass loss and duration of moult in Macaroni and Rockhopper Penguins. Ostrich 57:180-184.

The development of new feathers, loss of body mass and the duration of moult were investigated in Macaroni Penguins Eudyptes chrysolophus and Rockhopper Penguins E. chrysocome at Marion Island, southern Indian Ocean. New feathers began developing under the skin before the birds returned ashore to moult, and only began protruding through the skin about five days later when they were already over half their final length. Feather synthesis was complete by 21 days after the birds returned ashore. Loss of body mass was similar to previous observations for the species, but previous reports on the duration of moult do not take into account that moult begins while the birds are still at sea.     

THE FIORDLAND CRESTED PENGUIN EUDYPTES PACHYRHYNCHUS

Aspects of the biology of Eudyptes paclzyrhynchus nesting on the west coast of the South Island of New Zealand were studied over six seasons. Nests occur in small scattered groups on steep slopes covered with heavy rainforest, beneath which the birds are protected from temperature extremes. After about four months at sea, the breeding birds return to land at the height of the southern winter. They aggregate in small, loosely organized groups, breed annually and tend to retain the same nest-site and mate from year to year. They are ashore to breed for about 20 weeks before their chick departs. Incubation lasts for 31–36 days, and is undertaken in long shifts by both sexes in turn. It does not begin until the second and larger of the two eggs has been laid. The hatchling is guarded by the male for about three weeks, during which time it is fed almost daily by the female parent. The chick then joins a crèche and from then is fed by both parents until, at about 75 days old, it leaves for the sea. The parents also leave thereafter. Details are given of egg dimensions and weights, of egg loss, rates of chick-growth, the fate of twins and of the food brought to the chicks. Egg and chick losses are high. The heavy rainfall and frequent storms seem major causes of loss. The birds seem incapable of rearing more than one chick, and when two are hatched a size disparity soon appears leading to the death of the smaller, apparently through starvation. The adults moult annually in the forest, often on their nests, after some 60 to 80 days spent at sea fattening up for this event. They fast for about 25 days before their new plumage is sufficiently well grown to permit their return to feed. Their whereabouts out of the breeding season are unknown. Display and associated behaviour are complex. They involve many dramatic attitudes in which the flippers and crests feature prominently accompanied by loud vocalizations. In an Appendix figures are given for dimensions of breeding pairs and details of other morphological differences between the sexes and between members of the present species and its closely related congener E. robustus.     

Aggressiveness in king penguins in relation to reproductive status and territory location

King penguins, Aptenodytes patagonicus, vigorously defend small territories in very dense colonies. The egg-laying season lasts approximately 4 months, but only pairs that reproduce during the first half of the period succeed in fledging a chick. I examined various factors affecting aggressiveness of king penguins during the breeding season and focused on the differences between central and peripheral territories. Pairs on peripheral territories experienced twice as many encounters with avian predators as did central birds. The vast majority of peripheral birds were late breeders, indicating that reproductive success was very low among penguins defending a territory on the edge of the colony. Time invested in territory defence and rate of agonistic encounters between breeding neighbours increased from the incubation to the brooding period. Parents gave most threat displays to territorial neighbours when the chick was very young and just before crèche formation. Distance to colony edge was not related to aggressiveness in incubating birds, however, the rate of pecking and flipper blows increased from the edge to the centre during brooding. In addition, aggressiveness of breeding penguins towards travelling birds trespassing into their territory increased with distance to edge. Early breeders were not more aggressive than late breeders but the proportion of time spent in territory defence increased with the number of days a bird had spent incubating. As expected, I did not detect any sex difference in aggressive behaviour. Birds occupying territories on the beach were generally more aggressive during the incubation period than those located on the valley sides. Reproductive status (incubating versus brooding) and territory location were the main factors explaining the various levels of aggressiveness observed in breeding king penguins. Copyright 2000 The Association for the Study of Animal Behaviour.     

Survival costs of within‐ and between‐season mate change in the European blackbird Turdus merula

Many studies of socially monogamous birds discuss the adaptive role of between‐season partner change, but only a handful of them refer to the benefits of pair fidelity in terms of increased survival. Moreover, there are no studies describing the benefits of within‐season mate retention. Our data relating to an urban population of European blackbirds Turdus merula enabled us to test the dependence of survival on pair faithfulness. Because blackbirds divorce within and between seasons, we were able to test the influence of pair faithfulness on their within‐ and between‐season survival and mate fidelity. For this purpose, we used a multievent capture–mark–recapture (MECMR) statistical model, which is based on recapture rates and different pair states (faithful to mate, paired with new partner, or dead). Our study indicated that between‐ and within‐season survival depends on pair states: pair‐bond duration increases survival to the next capture occasion in both sexes. We found that the pair‐bond duration to the current partner increased the chances of being with the same partner during the next breeding occasion, although we failed to find any within‐season pair‐bond influence for females. Our results showed sex differences in mating at the end of the season: females had a much smaller chance of breeding with the current new partner in the next year. This study has demonstrated that within‐ and between‐season survival is dependent on mate retention, and we discuss this in the context of how searching for a new partner could affect the birds’ survival.