Social aspects of the termination of incubation behaviour in the ring dove (Streptopelia risoria)

The role of male and female ring doves (Streptopelia risoria) in the termination of incubation behaviour was studied first by observing heterosexual pairs (male and female) and homosexual pairs (female and female) (experiment 1). Male/female pairs incubate for 22 days whether squab or unhatched eggs are in the nest; female/female pairs incubate for 25 days or more. Males take the lead in terminating incubation. Another group of doves, separated from their (heterosexual) partners late in incubation, were exposed to one of four stimulus conditions: (a) an incubating dove; (b) a reproductively-inactive dove; (c) a reproductively-active dove; (d) visual isolation. Females extended the duration of their incubation when exposed to the sight of another dove, except when the stimulus dove was reproductively active. Males did not extend their incubation in response to these social cues. These social stimuli terminating incubation behaviour coordinate the withdrawal from the nest of male and female in preparation for the next breeding episode in this monogamous species.     

Sexual behaviour in the zebra finch Taeniopygia guttata: response to familiar and novel partners

On their introduction to a novel female, unpaired male zebra finches showed initial courtship, followed by a phase of nest soliciting. Pairing the partners changed the balance between these activities, speeding the transition from courtship to nest soliciting. This experience with the partner involved both the formation of a pair-bond, and changes in her familiarity, and it was the latter which was most important; hormonal changes were probably not involved. The behaviour is compared with that of doves and pigeons, and the possible role of aggression in the, causation of courtship is discussed.     

The effects of photoperiod on androgen-induced reproductive behavior in male ring doves, Streptopelia risoria

The effect of photoperiod on reproductive behavior in male ring doves (Streptopelia risoria) was studied in androgen-injected castrates maintained under long (16L:8D) or short (86:16D) photoperiods. Behavioral recordings were made over a 2-week period during which each male was paired with a female for 6.5 hr/day. There was some indication that males held on long days display higher levels of courtship activity during the initial period following pairing, but the evidence was not conclusive. Day length had no effect upon copulatory behavior. Long-day males exhibited consistently higher levels of nest building than short-day males, indicating that photoperiod affects building through some mechanism other than changes in endogenous androgen levels.     

Hypothalamic monoamine turnover in ring doves (streptopelia risoria), courting,incubating and brooding young

1. The turnovers of hypothalamic 5-hydroxytryptamine (5HT), dopamine (DA) and noradrenaline (NE) were measured in male and female ring doves (Streptopelia risoria) at three stages of the breeding cycle: courtship, 3 days after pairing; early incubation, 1–2 days after egg laying; and brooding, 1–3 days after the squabs had hatched.2. In both sexes plasma LH decreased progressively from courtship through incubation to brooding young. Crop sacs were fully developed in doves brooding young but not at other stages of the reproductive cycle, indicating increased concentrations of plasma prolactin.3. The turnovers of 5HT and DA in both sexes were significantly higher (P<0.001) in doves brooding young than in birds incubating eggs or nest building. The turnover of DA was higher in females than in males at the onset of incubation. The turnover of NE was lower (P > 0.01) in females at the onset of incubation than during courtship or brooding.4. Increased turnover of hypothalamic DA may be more closely related to brooding behaviour than to changes in prolactin or LH secretion.5. Increased hypothalamic 5HT turnover in brooding doves appears to be more directly related to crop sac development, and by inference increased prolactin secretion, than to depressed plasma LH concentrations.     

Effects of stimuli emanating from the nest on the reproductive cycle in the ring dove. I: Pre-laying behaviour

The course of several behavioural patterns could be influenced by controlling the state of the nest available to a pair of ring doves (Streptopelia risoria). These patterns were: wing-flipping, handling of nesting material, nest bowl occupancy, and nervous activities. In groups having to build nests, the onset of wing-flipping by the female occurred at a predictable time before egg-laying. It is argued that during nest-building a female influences the male to carry material to her by sitting in the nest bowl and wing-flipping. In pairs provided with a completed nest, the course of the pre-laying cycle was changed and the ‘typical’ sex roles did not emerge. The relationships between the male and female are discussed.     

Contributions of reproductive experience to observation-maintained crop growth and incubation in male and female ring doves

Previous work has established that experienced male ring doves (Streptopelia risoria) can maintain prolactin-dependent crop growth and readiness to incubate by observing an incubating partner. We report that this is also true for female ring doves. The role of experience in this phenomenon was examined in separate experiments with males and females. Observation of an incubating mate from 3 days after completion of egg laying is sufficient to maintain crop growth and incubation in both male and female ring doves in their second, but not in their first, reproductive cycle. Male and female doves in their first cycle must incubate for a greater part of the cycle before observation of an incubating mate is an effective stimulus; there are no differences between first and second cycle doves separated by a glass plate from the mate and nest 8 days after laying. Experience obtained within the first cycle apparently ensures that previously neutral stimuli come to elicit prolactin secretion. The effectiveness of these stimuli is reinstated early in a second cycle.     

Effects of septal lesions on the courtship behavior of male ring doves (Streptopelia risoria)

Male ring doves exhibit several androgen-dependent behavior patterns. Preliminary studies indicated that one of these, the nest-soliciting display, was selectively increased following septal lesions. In the present study castrated male ring doves received a septal lesion followed by daily intramuscular injections of 30 μg testosterone propionate (TP). Although one of the androgen-dependent displays, the bow-coo, was unaffected by the lesions, nest soliciting was significantly elevated during the period of hormone treatment. The restoration of nest-soliciting behavior in the males with septal lesions was even more rapid than that of unlesioned males receiving 200 μg TP/day, although after 12 days of treatment the performances of the latter came to approximate those of the males bearing septal lesions. Males that had received lesions in brain areas other than the septum were no more responsive to 30 μg of TP than were nonlesioned males receiving similar hormone treatment. It is suggested that the influence of the septum differs among the various androgen-dependent displays.     

The Functions of Song in the Serin

The function of song in the serin Serinus serinus was investigated by measuring variation in singing time and song flights by the male, and nest building by the female during the prelaying and laying period, and by correlating nest building, extra-pair copulation attempts and chasing of the female with male singing time and song flights between pairs. Both singing time and nest building varied in relation to the female fertile period, peaking at day −4. Moreover, nest-building activity correlated with singing time, but not song flights, between pairs. This suggests that song may have a function in stimulating the female to nest build or begin rapid yolk deposition. Pair copulations were not correlated with singing time or song flights either over days relative to laying or between pairs and pairs were not more likely to copulate in a given minute of observation when the male had sung in the previous minute than when he had not. However, extra-pair copulation attempts and chasing of the female showed a tendency to be negatively correlated with song flight but not singing time, between pairs. This suggests that song flight may have a function in discouraging sexual competition from other males.     

The stimulus to egg-laying in the Bengalese finch

The effects of mate and nesting facilities on the occurrence of egg-laying were examined in the Bengalese finch.
Egg-laying is unusual in isolated females and those kept in large groups. It is more common in monosexual pairs, and its incidence in them is not markedly altered by whether males can be heard or not. Females in heterosexual pairs usually lay within three weeks of pairing. A similar lag was found in pairs separated by bars, pointing to copulation being unnecessary.
Carrying of nest material to the nest box is mainly done by males. It is unusual in isolated birds, but occurs in monosexual and heterosexual pairs, and in pairs separated by bars.
Egg-laying is delayed in the absence of hay for nest building. A delay was also found in pairs separated by bars, when only the male was given nest material: this indicates that personal experience by the female is important. Heterosexual pairs deprived of nest boxes, but given nest material, were not recorded as laying.
It is concluded that egg-laying is stimulated by mate and nest material in a complex fashion. The various stimuli these provide interact to a greater or lesser degree to give the physiological and behavioural changes observed.     

The Roles of Stimuli from Young, Previous Breeding Experience, and Prolactin in Regulating Parental Behavior in Ring Doves (Streptopelia risoria)

In addition to stimulating crop "milk" formation in ring doves, prolactin (PRL) may promote the parental regurgitation behavior that transfers this "milk" to the young at the time of hatching. Although earlier studies suggest that previous breeding experience is an important modulator of PRL-induced parental regurgitation behavior in ring doves, the ways in which experience, hormones, and stimuli from young interact to promote parental behavior have not been well characterized in this species. In the first study, untreated, nonbreeding female doves with and without previous breeding experience were given 10 daily parental behavior tests (2 h/day) with a hungry 5- to 10-day-old foster squab. Experienced females exhibited a higher incidence of regurgitation behavior, defensive behavior, and crouching or sitting in the nest than did inexperienced females. In a second study, nonbreeding females were given 10 daily tests for parental behavior while they received sc injections of ovine PRL or vehicle. Prolactin reduced squab-directed aggression and increased the incidence of regurgitation feeding behavior of foster squabs in both experienced and inexperienced females. However, the average number of regurgitation feeding acts displayed by those PRL-treated females that showed the behavior was over eight times higher in experienced females than in inexperienced females. Previous experience also enhanced the stimulatory effects of PRL on defensive behavior and crouching or sitting in the nest. The parental behavior exhibited by nonbreeding, PRL-treated experienced females was qualitatively and quantitatively similar to that observed in normally breeding females during a single test with their own hungry 5- to 10-day-old squabs. These findings indicate that PRL and previous breeding experience both enhance the parental responsiveness of nonbreeding female doves and that under optimal hormonal, experiential, and squab exposure conditions, nonbreeding doves exhibit levels of parental activity that rival those of normally breeding parents.     

Egg fertility and prolactin as determinants of reproductive recycling in doves

When a pair of male and female ring doves in breeding condition is introduced in a breeding cage containing a nest bowl and a supply of nesting material, a regular and predictable sequence of behavioral changes can be observed. A complete breeding cycle consists of courtship and nesting (7–10 days), incubation (14–15 days), and parental care (21 days). A new cycle (recycling) starts following the departure of the fledglings. This study concerns itself with the occurrence of recycling before completion of a breeding cycle, with a special reference to the fertility of eggs. The fertility of eggs before and after oviposition regulates the timing of recycling. Laying infertile eggs as a result of having mated with impotent males (castrated + oil or castrated + testosterone proprionate) and then sitting on such eggs led to a 100% recycling with the shortest latency. In contrast, no doves recycled in the normal breeding pairs (females paired with intact males) until eggs were hatched and squabs fledged. For bird laying fertile eggs and sitting on infertile eggs or vice versa, half recycled, while the other half did not. The possibility that prolactin plays a role in mediating the onset of recycling was tested, and the significance of the results was discussed.     

The effect of an androgen inhibitor on behavior and testicular morphology in the stickleback Gasterosteus aculeatus

It is generally held that the decline in courtship which is seen at the beginning of incubation during the reproductive cycle of the male ring dove (Streptopelia risoria) is the result of changes in endocrine secretion rather than changes in response to the external situation. To test this hypothesis, male ring doves proceeding through a cycle with their mates were tested at selected intervals to determine whether there was a decline in courtship behavior in the course of a reproductive cycle. Four conditions were examined. Inexperienced and experienced males were tested with a stimulus female in two situations; once after the mate and nest were removed from the home cage, and once after the mate only was removed. In the former situation the male courted a stimulus female irrespective of the stage of the cycle he had reached with his mate. In the latter situation, as incubation with the mate progressed, males continued to incubate when the stimulus female was introduced. Thus, the male's display of courtship during the reproductive cycle is influenced by the external stimulus situation presented by the female and the nest.     

BREEDING BIOLOGY OF THE BEARDED VULTURE IN SOUTHERN AFRICA,PART I: THE PRELAYING AND INCUBATION PERIODS

Brown, C. J. 1990. Breeding biolo of the Bearded Vulture in southern Africa, Part I: The pre-laying and incubation periods. Ostrich 61: 24–32.

In southern Africa the Bearded Vulture Gpaetus barbatus lays its eggs in mid-winter. between the second half of May and the first week of July. Pairs became more active in their nesting areas about six weeks before laying and usually roosted there at night. Courtship flights were less frequent and demonstrative than in Eurasian birds and took place mainly in the late afternoons. During the pre-laying period most nest visits (77%) were to bring nesting material, 92% by the male. All nesting material was arranged by the female. Copulation was always preceded by allopreening, and occurred most frequently in the mornings. No copulation or courtship display took place after the first egg had been laid. Of 18 clutches, 16 (89%) contained two eggs and the remainder one egg. The laying interval was usually 3–5 days (range 2–9 days). Incubation started with the first egg and was evenly shared by both parents during the day, but only the female incubated at night, individual pairs maintained distinctive nest attendance and foraging period timetables, which allowed sufficient time for self-foraging by both parentes. No food was brought into the nest during the pre-laying and incubation periods, but in some pairs food was cached in nearby potholes in cliffs. The incubation period was 56–57 days.     

THE BIRDS OF BLYTHSWOOD AND SOME NOTES ON BIRDS OF THE DISTRICT

Wintle, C. C. &; Taylor, P. B. 1993. Sequential polyandry, behaviour and moult in captive Striped Crakes Aenigmatolimnas marginalis. Ostrich 64:115-122.

Captive Striped Crakes showed sequential polyandry, the female laying for a second male when the clutch of her first mate was about to hatch. Where aviary space permitted each male set up a breeding territory and each female defended a larger area encompassing the territories of one or two males. Non-territorial subordinate males and females did not breed. The female initiated breeding by attracting the male and soliciting copulation, and the male incubated the eggs and cared for the young. Incubation took 17–18 days, the chicks left the nest at 4–5 days of age and were fully grown and capable of flight at 46–53 days. Breeding occurred from September to March and males normally reared two broods per season. Territoriality was evident only during the breeding season. Juvenile plumage was a duller version of the sexually dimorphic adult plumage; post-juvenile moult bean at 13–15 weeks and was complete at 21 weeks. Remex moult was simultaneous and a complete moult regular1 occurred twice a year in adults, in December and April (males) and September and March/April (females).     

Gonadal hormones determine sex differences in timing of incubation by doves.

Male and female ring doves express a sexually dimorphic pattern of incubation. The dimorphism is temporal rather than motoric. The male incubates for a block of time in the middle of the day and the female incubates the rest of the time. The present study explored the role of gonadal hormones in the control of the temporal dimorphism. Female-female pairs incubated their eggs, but it could not be predicted which of the partners would be sitting on the nest at any given time. Male-male pairs did not incubate and instead destroyed the nests that were provided and displayed aggressive behavior. Some intact males incubated when paired with gonadectomized males, although the castrates tended to ignore the nest. In contrast, when castrated birds were given heterotypical hormonal replacement therapy, they and their same-sex partners incubated the eggs that had been provided, with the gonadectomized birds sitting at a time appropriate to the hormonal state. The results indicate that gonadal hormones influence not only the expression of incubation behavior, but also its phase and duration.     

Behavioral predictors of pairing success in rhesus macaques (Macaca mulatta)

Pair housing is one of the most important components of behavioral management for caged macaques; however, it can result in aggression and injury if partners are incompatible. Knowing when to proceed and when to stop social introductions can be challenging, and can have consequences for the partners. We examined whether behavior early in social introductions predicted success (i.e., partners remained cohoused with full contact for at least 28 days) in 724 female–female and 477 male–male rhesus macaque pairs. We took cage side one–zero focal observations on pairs during the first 2 days of full contact, recording social and aggressive behaviors. The majority of pairs (79.6% of female and 83.0% of male) were successful. The most common behaviors exhibited by pairs during these observations were maintaining proximity, tandem threats, and anxiety. Mounting was also relatively common in male pairs. Grooming and close social contact (e.g., touching) were not common in our study. Several behaviors observed on Day 1 significantly predicted pairing success. For females, these included proximity, tandem threat, rump present, mount, and groom. Day 1 predictors of success for male pairs included proximity, tandem threat, rump present, mount, and social contact. Fewer behaviors predicted success on Day 2. Maintaining proximity on Day 2 predicted success for both sexes, but tandem threat predicted success only for females. Behaviors that predicted incompatibility for females on Day 1 included displace, grimace, threat, bite, and other aggressive contacts. Day 1 predictors of separation for male pairs were displaced, grimace, and abnormal behavior. The only Day 2 behavior that correlated with incompatibility was grimace, which was predictive for males. Interestingly, aggression did not predict incompatibility for male pairs. Identifying behaviors exhibited by monkeys early in the pair introduction that are predictive of long-term compatibility can shape pairing decisions, reducing later stress and potential injury.     

Interactive vocal communication at the nest by parent Great Tits Parus major

Although most bird species show monogamous pair bonds and bi‐parental care, little is known of how mated birds coordinate their activities. Whether or not partners communicate with each other to adjust their behaviour remains an open question. During incubation and the first days after hatching, one parent – generally the female – stays in the nest for extended periods, and might depend on acoustic communication to exchange information with its mate outside. The Great Tit Parus major is an interesting study system to investigate intra‐pair communication at the nest because males address songs to their mate while she is in the nest cavity, and females answer the male from the cavity with calls. However, the function of this communication remains unknown. In this study, we recorded the vocalizations and observed the resulting behaviour of Great Tit pairs around the nest at different breeding stages (laying, incubation and chick‐rearing). We observed vocal exchanges (vocalization bouts, alternated on the same tempo, between the female inside the nest and her male outside) in three contexts with different outcomes: (1) the female left the nest, (2) the male entered the box with food, and the female then used specific call types, (3) mates stopped calling but did not leave or enter the nest. The structure of vocal exchanges was globally stable between contexts, but females used calls with an up‐shifted spectrum during exchanges, at the end of which they left the nest or the male entered the nest. Birds vocalized more and at higher tempo during exchanges that ended up in feeding inside the nest. Birds also vocalized more during exchanges taking place during laying – a period of active mate guarding – than during incubation. We conclude that vocal exchanges could signal the females’ need for food and the males’ mate guarding behaviour, and discuss other possible functions of this communication.     

Pairing Patterns in Japanese Beetles (Popillia japonica Newman): Effects of Sex Ratio and Time of Day

Size-related patterns between unpaired and paired individuals and between males and females of a given pair give clues about both a species' sexual behavior and the environmental factors affecting its sexual behavior. We studied the mating patterns of Japanese beetles (Popillia japonica) in east–central Illinois. The frequency of male–female pairs varied significantly among days and within a day, with pairs being significantly more common in the morning and the evening. The sex ratio on the food plants was significantly male biased, but although the sex ratio fluctuated among days and among time periods, the variation in the frequency of mating pairs was not explained by variation in the sex ratio. We found no assortative pairing with respect to size, but sizes of paired and unpaired individuals did differ. Paired females were larger than unpaired females at all time periods. In contrast, paired males were larger at 0700 and smaller at 1000, and little difference existed at other times of the day. The size of males and females, sex ratio, and pairing frequency also differed among days. Much of this variation in size and pairing frequency was related to a seasonal effect: later in the summer, beetles of both sexes were smaller and pairs were less common. Interestingly, pairs were also less frequent on days with higher average temperatures. This between-day variation in pairing, in combination with the within-day pairing differences, suggests that the temperature may alter the cost, and hence likelihood, of pairing in this species.     

Handicapped females receive more feedings during incubation from their mates: support for the female nutrition hypothesis

The female nutrition hypothesis posits that provisioning intensity of incubating females by their mates may depend on female needs and ensure proper incubation and a corresponding high hatching and breeding success of breeding pairs. Here, we have handicapped female pied flycatchers Ficedula hypoleuca at the beginning of incubation by clipping two primaries on each wing and filmed nests during incubation and later nestling provisioning to estimate male involvement in incubation feeding at the nest and in offspring care. Incubation feeding was more frequent at late nests. Correcting for this seasonal effect, incubation feeding was significantly affected by treatment and twice as high at experimental as at control nests. There was no effect of the experiment on female incubation attendance. The handicap did not result in any effect on hatching and breeding success, nestling growth and male or female provisioning and mass at the end of the nestling period. Males adjust their incubation feeding activity at the nest to female energetic requirements during incubation.     

Behavioural and body mass changes before egg laying in the Barn Owl: cues for clutch size determination?

To investigate laying decision and clutch size determination in indeterminate layers, we analysed in-nest activity (nest presence, and copulation, prey deliveries, and entrance frequencies) and female body mass change, as well as their relation to clutch size variation in five Barn Owl pairs (Tyto alba) nesting in eastern France. Body mass of the female and behaviour [copulation frequency, entrance frequency, and prey delivery to the nest by the male (in number and mass)] were monitored using an automated weighing system and a video camera. There was a consistent change of behaviour and foraging activity among pairs ca. 18 days before laying indicating that the females may be tied to the nest at this time. Barn Owls being indeterminate layers have their clutch size determined at the oviposition of the first egg of the clutch. Window correlation analyses between the clutch size and the female body mass gain indicate that the clutch size might be determined no later than a few days before the laying of the first egg. Our results suggest that female Barn Owls may use the pre-laying period to determine the clutch size using cues such as the male food deliveries (a proxy for male quality).