A study of distress calls of song, swamp, and white-throated sparrows (Aves: Fringillidae). I. Intraspecific responses and functions

1972 ◽  
Vol 50 (12) ◽  
pp. 1501-1512 ◽  
Author(s):  
Raymond A. Stefanski ◽  
J. Bruce Falls

Distress calls, recorded from birds captured in mist nets, were played to territorial pairs in successive stages of the breeding cycle. Responses included approach, movement about the speaker, alarm calls, and displays. Latent time to response, closeness of approach, and numbers of movements and calls were measured.Males of all three species responded strongly in the nest building and egg-laying stage and weakly in the incubation and early nestling stage, when behavior is generally cryptic. A major peak of response, characterized by close approach and distraction displays, occurred in the late nestling and fledgling stage, when young are capable of emitting distress calls. Responses declined as juveniles became independent.Responses of females were generally weaker and more variable but the major peak was still evident.When a red squirrel or blue jay was exposed during playback to white-throated sparrows in the late nestling and fledgling stage, diving attacks and distraction displays were directed toward the "predator."Distress calls, normally given by a bird seized by a predator, may startle the predator and elicit harassment and distraction behavior from other birds. A responding individual learns the characteristics and location of the predator and may facilitate the escape of its mate or young.

Behaviour ◽  
2012 ◽  
Vol 149 (1) ◽  
pp. 81-98 ◽  
Author(s):  
Michał Gąska ◽  
Przemysław Grela ◽  
Janusz Kloskowski

AbstractIn monogamous birds, early male parental effort, such as nest building, may serve as a post-mating sexually-selected display allowing female assessment of male quality. We examined the functional significance of male nest building and the potential role of nest size as a sexually-selected signal in the red-necked grebe ( Podiceps grisegena), a species with high mate fidelity. Time-activity budgets showed that no behaviour was performed exclusively by one sex in the pre-laying period, but males spent significantly more time nest building and were more often involved in aggressive intra- and interspecific interactions. Nest building in pairs attempting a second brood was also performed predominantly by males. Greater participation in nest construction by males allowed females to allocate more time to self-maintenance activities in the period prior to egg-laying. The positive relationship found between the relative contribution of males to nest building and later to brood provisioning indicates that male nest building is an honest indicator of future paternal effort. Males obtained copulations solicited by females proportionally to the time spent on nest building, and the extent of male participation in nest construction was of importance for explaining variation in clutch size. Nest size itself is not very likely to be sexually selected in red-necked grebes, as it was found to depend on nest site conditions such as water depth and exposure to wave action. We suggest that greater investment of males in energetically demanding pre-laying activities is functionally similar to post-mating courtship feeding; it constitutes males’ indirect contribution to clutch production and may help to negotiate the relative investment each sex makes in the different stages of the breeding cycle. The results support the idea that, in monogamous birds, naturally selected male characters related to parental care may evolve into important sexual signals to females, although not into extreme displays.


2000 ◽  
Vol 48 (4) ◽  
pp. 347 ◽  
Author(s):  
Cristina Davey ◽  
Alan Lill ◽  
John Baldwin

Parameters that influence blood oxygen carrying capacity (whole-blood haemoglobin content, haematocrit and red blood cell count) were measured in samples of 30 breeding, adult short-tailed shearwaters (Puffinus tenuirostris) on Phillip Island, Victoria at seven key stages of their reproductive cycle. The aim of the investigation was to determine whether variation in blood oxygen carrying capacity during the birds’ 7-month breeding cycle was correlated with variation in the energy demands they experienced or was an incidental by-product of other physiological changes. All the blood parameters varied significantly during breeding, but the pattern of variation was only partly correlated with the likely pattern of changing energy demand imposed on parents by their schedule of breeding activities. The main trend conceivably related to energy demand was that significantly higher values were recorded for these blood parameters during the nestling stage than earlier in the breeding cycle. This could have reflected the high costs of the very long foraging trips undertaken by parents feeding nestlings, but it could also have occurred in preparation for the long migration undertaken soon after breeding finished. It involved an ~10% increase in blood oxygen carrying capacity above the lowest mean value recorded during the breeding cycle and so other mechanisms must also be employed to achieve the increase in aerobic metabolism likely to be required at this stage. The lack of adjustment of blood oxygen carrying capacity to energy demand early in the breeding cycle suggests that either oxygen delivery was not a rate-limiting process for aerobic metabolism at that time or that delivery was enhanced through other mechanisms. At egg laying, females had a lower haematocrit and erythrocyte count than males, which could be attributable to either estrogenic suppression of erythropoiesis or an increase in osmotic pressure of the blood associated with yolk synthesis. Immature, non-breeding birds attending the colony were of similar mass to adults, but did not show the increase in the parameters determining blood oxygen carrying capacity that occurred in adults later in the breeding cycle. Factors other than changing energy requirements (dehydration, burrow hypoxia and differential responsiveness to capture stress) that might have influenced the pattern of variation in blood oxygen carrying capacity of adults during breeding are discussed.


The Auk ◽  
1979 ◽  
Vol 96 (1) ◽  
pp. 56-67 ◽  
Author(s):  
Shoshana Ashkenazie ◽  
Uriel N. Safriel

Abstract Pair formation of Calidris pusilla near Barrow, Alaska occurs 3-6 days after the territory is established. The pair is then engaged in nest scraping displays during 2-3 days, in which 10-12 scrapes are made by the male and examined by the female. Eventually 2-3 scrapes are lined by the female, and in one of these the first egg is laid 4-6 days after pairing. During the egg-laying period further lining is performed by the female and partial incubation takes place by both sexes. Continuous incubation commences 8 h prior to laying of the 4th egg. Male and female alternate in incubation: in the first 2 days a turn lasts 3-5 h, and the duration gradually increases up to 13-14 h during the 2nd week. Long incubation turns reduce the number of approaches to the nest and may therefore reduce the chances of it being discovered by predators. The incubating bird is intermittently engaged in egg-rolling and in camouflaging the nest by bending adjacent grass blades over its back, and is constantly alert. The off-duty bird may feed 2-3 km away from the nest. The eggs hatch after 20 days of incubation, all within 1 day. Females desert the family 2-8 days after hatching: they desert late if hatching is early, and early if hatching is late in the season. After female departure the family moves from the nesting territory, typically in a high-centered polygonal area, to establish a home range as far as 2-3 km away, often in a low-centered polygonal area. During the first 6-8 days after hatching, the male prepares each evening a scrape for night brooding. After fledging, the male and young join wandering flocks.


The Auk ◽  
2004 ◽  
Vol 121 (1) ◽  
pp. 110-117 ◽  
Author(s):  
Valentin Amrhein ◽  
Hansjoerg P. Kunc ◽  
Marc Naguib

Abstract Seasonal patterns of singing activity of male birds have been thoroughly studied, but little is known about how those patterns vary with time of day. Here, we censused mated and unmated male Nightingales (Luscinia megarhynchos) at four different hours of the day throughout the breeding cycle. In unmated males, singing activity increased until the young hatched in their neighborhood, and the seasonal variation was similar at each of the four hours of the day. In mated males, however, the seasonal patterns of singing activity differed between hours of the day. In morning (about the hour of egg-laying) and during the dusk chorus, the singing activity of mated males was strongly influenced by the females' reproductive state: singing activity was low before egg-laying and during incubation, but high during the egg-laying period. In the dawn chorus, however, singing activity showed a similar seasonal pattern in mated and unmated males and was high until late stages of the breeding cycle. Our results suggest that the social context influences singing behavior to a varying degree across the season, and that this variation also depends on time of day. The hour of data collection thus is an important but often neglected factor when seasonal changes of singing activity are studied.


1976 ◽  
Vol 54 (3) ◽  
pp. 343-354 ◽  
Author(s):  
N. R. Liley

Female doves were held under long (16 h per day), or short (8 h per day) photoperiod and exposed to actively courting males for 4.5 h per day for 15 days. The occurrence of egg laying and nest building was recorded daily. Behavioural observations were recorded for 15 min on alternate days.Seven out of eight long-photoperiod females laid eggs, whereas only one of nine short-photoperiod females began egg laying. Soliciting by the female and nest building involving male and female are the best indicators of a female's readiness to begin breeding. The occurrence of these activities is correlated with the growth of follicles and oviduct. Copulation and associated behaviours are not correlated with follicle and oviduct growth, and appear to be controlled by factors different from those governing courtship behaviour associated with the nest site.


Behaviour ◽  
2004 ◽  
Vol 141 (4) ◽  
pp. 451-467 ◽  
Author(s):  
Rianne Pinxten ◽  
Lutgarde Arckens ◽  
Els van Duyse ◽  
Marcel Eens ◽  
Veerle Darras

AbstractThe apparent ability of plasma testosterone (T) and corticosterone (B) levels to fluctuate rapidly in response to agonistic interactions, suggests that these hormones may play an important role in an animal's acute behavioural response during such interactions. In the present study, free-living male great tits, Parus major, were subjected to a simulated territorial intrusion (STI) during the egg laying, incubation and nestling stage of first broods. Plasma T and B levels of challenged males were compared to those of control males matched for breeding stage, day in breeding stage, and time of day. Plasma B levels were significantly higher in challenged males compared to control males during the egg laying and incubation stage but not during the nestling stage. On the other hand, challenged males had significantly lower plasma T levels than control males throughout the breeding cycle. While having low plasma T and elevated plasma B levels, challenged males showed a vigorous and unrelenting territorial response to the STI. Plasma T and B levels of challenged males did not correlate with the intensity of the behavioural response to the STI. These findings do not agree with the predictions of the 'challenge hypothesis' that males exposed to a territorial challenge while having breeding baseline T levels will respond with an increase in T or that T correlates with the intensity of aggression during a challenge. Together, our findings suggest a role for B rather than T in the regulation of territorial defence in male great tits.


1976 ◽  
Vol 54 (9) ◽  
pp. 1409-1422 ◽  
Author(s):  
N. R. Liley

Female ring doves held under long (16 h per day) or short (8 h per day) photoperiods were treated daily for 15 days with saline, estrogen, or progesterone, alone or in combination. Seven days after the start of hormone therapy females were placed with reproductively active males for 4 h per day for 9 days. There was no difference in egg-laying, courtship, and nest-building by control birds under the two photoregimes.Ovarian follicles remained small in all birds receiving hormone treatment. Oviducts of birds receiving progesterone alone remained small in the short-photoperiod group, but at long photoperiods oviducts became enlarged. Estrogen stimulated oviduct growth at both photoperiods. The combined hormone treatment resulted in considerably greater oviduct development than estrogen alone, and in this case the oviducts of birds under long photoperiod were significantly heavier than those of short-photoperiod birds.Female soliciting and nest-building activity remained low in progesterone-treated females under short photoperiod, but increased rapidly under long photoperiod. Birds treated with estrogen and estrogen and progesterone performed considerable soliciting and nest-building. There was a marked tendency for birds under long-photoperiod conditions to be more active in nest-oriented behaviour. Copulatory behaviour by the female (begging and sexual crouch) occurred infrequently in all hormone-treated birds.


2003 ◽  
Vol 81 (10) ◽  
pp. 1685-1690 ◽  
Author(s):  
Sharon A Gill ◽  
Spencer G Sealy

During nest defence, yellow warblers (Dendroica petechia) give "seet" and "chip" calls. Seet calls are given preferentially toward brood parasitic brown-headed cowbirds (Molothrus ater) during the yellow warblers' egg-laying period, whereas chip calls are given toward mammalian and avian nest predators throughout the nesting period. In this study, we investigated two possible functions of seet and chip calls during nest defence by playing alarm calls to nesting yellow warblers. We tested whether nest owners give seet and chip calls during defence to alert their offspring and their mates about nest threats and, in the latter case, whether the alarm calls differ in function depending on nesting stage. In response to playbacks, nestlings remained inactive for a significantly longer period when chip calls were played than when seet calls were played. Female yellow warblers returned to their nesting areas more quickly when seet calls were played than when chip calls were played, but pairs were equally likely to return to the nesting area in response to both call types. These findings suggests that both seet and chip calls alert mates but that only chip calls function to alert nestlings of potential danger.


Apidologie ◽  
2021 ◽  
Author(s):  
Jordan T. Ryder ◽  
Andrew Cherrill ◽  
Helen M. Thompson ◽  
Keith F. A. Walters

AbstractThe performance of Bombus terrestris micro-colonies fed five diets differing in pollen species composition and level of nine essential amino acids (EAA; leucine, lysine, valine, arginine, isoleucine, phenylalanine, threonine, histidine, methionine) was assessed for 37 days by recording total biomass gain, nest building initiation, brood production (eggs, small and large larvae, pupae, drones), nectar, and pollen collection. Stronger colony performance was linked to higher amino acid levels but no consistent differences in biomass gain were recorded between mono- and poly-species diets. Poorest performance occurred in micro-colonies offered pure oilseed rape (OSR) pollen which contained the lowest EAA levels. Reduced micro-colony development (delayed nest initiation and lower brood production) was related to OSR proportion in the diet and lower EAA levels. Results are discussed in relation to selection of plant species in the design of habitats to promote bee populations.


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