The Breeding Behaviour of the Pink-Footed Goose: Parental Care and Vigilant Behaviour During the Fledging Period

Behaviour ◽  
1978 ◽  
Vol 65 (1-2) ◽  
pp. 62-87 ◽  
Author(s):  
Lazarus John ◽  
Inglis I.R.

In this study we describe the pattern of parental investment in the pink-footed goose (Anser brachyrhynchus) during the fledging period in Iceland, concentrating particularly on the analysis of vigilant behaviour as one important element of parental care. We quantify parental investment, and its cost to the parent, by comparing the behaviour of parents with that of 'pairs' of adults without young (most of which are probably failed breeders). Each partner's strategy of investment is not expected to be purely selfish in this long-term pair-bonding species, and the sex differences in parental care are examined in this light. The time budgets of parents and pairs differed, parents walking more, grazing more and preening less. Parents also spent more time in the extreme head up posture and less in the head low and head on back postures than pairs but time devoted to the head up posture was the same for both. Brood size had no effect on the time budget. Time spent extreme head up declined over the study period in parents but not in pairs. Spacing patterns and behaviour varied independently in non-breeding birds but families sat closer to other geese when the vigilance level of the parents was low (i.e. in the head on back or head low postures) than when it was high (the head up or extreme head up postures). All agonistic encounters between parents and non-breeders were both initiated and won by the parents. Tied encounters occurred between birds of equivalent status in terms of brood size or non-breeding group size. The potential sources of parental care are summarized (Table 6) and, after considering the evidence for each, it is concluded that (apart from brooding) two types of parental investment are made by parents: (1) enhancement of offspring feeding efficiency by reducing competition through agonistic behaviour, and perhaps avoidance; and (2) protection from predators by (a) active defence, (b) seeking proximity with other geese when resting, and (c) visual scanning for predators (mainly by the male) using the extreme head up posture. Parents paid for this investment by devoting less time to preening and sleeping. The male's investment in predator vigilance was made at the cost of a reduced feeding time and to compensate for this he pecked at a faster rate than his mate. These sex differences are explicable in terms of earlier differences during incubation. The adoption of unrelated goslings was observed and the implications of the phenomenon are discussed. For individuals in non-breeding groups the time spent extreme head up declined as group size increased. The functional significance of this finding is discussed and it is concluded that in sitting groups extreme head up is probably used to scan for predators.

Behaviour ◽  
1978 ◽  
Vol 65 (1-2) ◽  
pp. 62-87 ◽  
Author(s):  
Lazarus John ◽  
Inglis I.R.

In this study we describe the pattern of parental investment in the pink-footed goose (Anser brachyrhynchus) during the fledging period in Iceland, concentrating particularly on the analysis of vigilant behaviour as one important element of parental care. We quantify parental investment, and its cost to the parent, by comparing the behaviour of parents with that of 'pairs' of adults without young (most of which are probably failed breeders). Each partner's strategy of investment is not expected to be purely selfish in this long-term pair-bonding species, and the sex differences in parental care are examined in this light. The time budgets of parents and pairs differed, parents walking more, grazing more and preening less. Parents also spent more time in the extreme head up posture and less in the head low and head on back postures than pairs but time devoted to the head up posture was the same for both. Brood size had no effect on the time budget. Time spent extreme head up declined over the study period in parents but not in pairs. Spacing patterns and behaviour varied independently in non-breeding birds but families sat closer to other geese when the vigilance level of the parents was low (i.e. in the head on back or head low postures) than when it was high (the head up or extreme head up postures). All agonistic encounters between parents and non-breeders were both initiated and won by the parents. Tied encounters occurred between birds of equivalent status in terms of brood size or non-breeding group size. The potential sources of parental care are summarized (Table 6) and, after considering the evidence for each, it is concluded that (apart from brooding) two types of parental investment are made by parents: (1) enhancement of offspring feeding efficiency by reducing competition through agonistic behaviour, and perhaps avoidance; and (2) protection from predators by (a) active defence, (b) seeking proximity with other geese when resting, and (c) visual scanning for predators (mainly by the male) using the extreme head up posture. Parents paid for this investment by devoting less time to preening and sleeping. The male's investment in predator vigilance was made at the cost of a reduced feeding time and to compensate for this he pecked at a faster rate than his mate. These sex differences are explicable in terms of earlier differences during incubation. The adoption of unrelated goslings was observed and the implications of the phenomenon are discussed. For individuals in non-breeding groups the time spent extreme head up declined as group size increased. The functional significance of this finding is discussed and it is concluded that in sitting groups extreme head up is probably used to scan for predators.


The Auk ◽  
1987 ◽  
Vol 104 (4) ◽  
pp. 688-693 ◽  
Author(s):  
Martin Schindler ◽  
Jürg Lamprecht

Abstract Positive correlations of brood size with some parental activities [vigilance (in females), approaching young (in males and females), and attack (in males)] and a negative correlation of female feeding time with brood size were found in a sample of 23 semicaptive Bar-headed Goose (Anser indicus) families. Detailed examination of these correlations suggests that some components of parental care in geese represent "shared parental investment" (Lazarus and Inglis 1978, 1986). The benefits of parental care are divided among the offspring, so that in precocial birds, as in altricial birds, clutch size may be adapted to selection pressures that act after the young hatch.


1998 ◽  
Vol 76 (7) ◽  
pp. 1382-1387 ◽  
Author(s):  
Claudio Carere ◽  
Enrico Alleva

We analysed sex differences in parental behaviour in a Mediterranean population of common swifts (Apus apus). Females attended the nest and fed the chicks at a higher rate than males and were more in contact with the nestlings during the first days after hatching, while no sex differences were found in other parameters measured. For larger broods no quantitative sex differences were observed in meal-delivery and brooding time, while for small broods the rate of feeding by males was lower than the rate of feeding by females, and males attended the nest less than females. No sex differences were observed at the early nestling stage, but males attended the nest less than females later in the nestling stage. No extra-pair breeding activity was observed. These results suggest that males reduce parental care when the energy requirements of the chicks decrease, while females do not.


1994 ◽  
Vol 72 (3) ◽  
pp. 533-540 ◽  
Author(s):  
Laura M. Seddon ◽  
Thomas D. Nudds

Competing hypotheses that have been advanced to explain the phenomenon of posthatch brood mixing by waterfowl can be distinguished by whether they assume that adults experience costs in rearing nidifugous offspring. To test this, time budget data were collected for giant Canada geese (Branta canadensis maxima) at Cambridge, Ontario, in 1990. Breeding adults with broods devoted more time to vigilance (p = 0.001) and less time to feeding (p = 0.001) than adults that hatched clutches but were without broods, suggesting a cost to rearing nidifugous young. However, as goslings matured, parents allocated less time to vigilance (p < 0.001) and more time to locomotion (p = 0.005), and time spent feeding did not change (p = 0.336). In addition, brood size did not affect the time parents allocated to vigilance (p = 0.543) or feeding (p = 0.727), suggesting that caring for additional young has negligible effects on parents. Goslings were selective about the adult with which they associated (they were positioned closer to females than to males), but neither brood size nor brood age affected the feeding time of goslings (p = 0.94 and 0.76, respectively) or time spent vigilant (p = 0.22 and 0.69, respectively), suggesting that goslings gained no obvious advantage from greater foraging opportunities or better predator detection by congregating in larger broods.


2008 ◽  
Vol 4 (4) ◽  
pp. 334-337 ◽  
Author(s):  
Sinead English ◽  
Hansjoerg P Kunc ◽  
Joah R Madden ◽  
Tim H Clutton-Brock

In species where young are provisioned by both parents, males commonly contribute less to parental care than females, and are less responsive to variation in begging rates. Similar differences in the care of young occur among adults in cooperative breeders, but fewer studies have investigated whether these are associated with differences in responsiveness. Here, we present results from a playback experiment investigating responsiveness to begging in the meerkat ( Suricata suricatta ), a cooperatively breeding mammal. Although increased begging rate raised the feeding rate of adults of both sexes, there was no consistent tendency for females to be more responsive than males. However, when we examined changes in the proportion of food items found that were fed to pups (generosity), we found that females were more responsive than males to increased begging rate. These results can be explained in terms of sex differences in dispersal: in meerkats, females are philopatric and receive considerable benefits from investing in young, both directly, by increasing group size, and indirectly, by recruiting helpers if they inherit the breeding position. In addition, they emphasize that generosity provides a more sensitive measure of responsiveness to begging than feeding rate, as it accounts for variation in foraging success.


1985 ◽  
Vol 63 (9) ◽  
pp. 2114-2120 ◽  
Author(s):  
Shirley J. Rushforth Guinn ◽  
Bruce D. J. Batt

Time budgets of pintail brood hen behaviour were collected at Oak Hammock Marsh, Manitoba, from June to August 1979. Hens spent 60.8% of their time at self-maintenance activities (feed, comfort movements) and 34.6% of their time at dominant parental care activities (alert, lead, follow). Hens with large broods allocated more time to self-maintenance than did hens with small broods. Time spent at parental care activities did not vary with brood size. The total time spent at parental care activities was higher for class I than class II broods. However, this pattern was not consistent across activities. Brood age did not influence time spent at self-maintenance. Hens spent more time at self-maintenance (feeding) and less time at parental care in late than in early season. We related this to the hen's need to recover weight lost during incubation, to acquire energy for a complete body plumage molt, and to prepare for fall migration. This paper describes patterns of time allocated to parental care. We conclude that estimates of costs of parental investment during the brood rearing period are also required.


2021 ◽  
Vol 9 ◽  
Author(s):  
Wenxia Wang ◽  
Long Ma ◽  
Maaike A. Versteegh ◽  
Hua Wu ◽  
Jan Komdeur

Life-history theory predicts that increased resource allocation in current reproduction comes at the cost of survival and future reproductive fitness. In taxa with biparental care, each parent can adjust investment on current reproduction according to changes in their partner’s effort, but these adjustments may be different for males and females as they may have different reproductive strategies. Numerous theoretical and empirical studies have proposed the mechanism underlying such adjustments. In addition, the value of the brood or litter (brood size) has also been suggested to affect the amount of care through manipulation of brood size. While the two conditions have been studied independently, the impact of their interplay on potential sex-dependent future reproductive performance remains largely unknown. In this study, we simultaneously manipulated both care system (removal of either parent vs. no removal) and brood size in a burying beetle (Nicrophorus vespilloides) to understand their joint effect on reproductive allocation and trade-off between current and future reproduction. Our results show that males compensated for mate loss by significantly increasing the level of care regardless of brood size, while females exhibited such compensation only for small brood size. Additionally, with an increase in allocation to current reproduction, males showed decreased parental investment during the subsequent breeding event as a pair. These findings imply a dual influence of parental care system and brood size on allocation in current reproduction. Moreover, the impact of such adjustments on sex-dependent differences in future reproduction (parental care, larvae number, and average larval mass at dispersal) is also demonstrated. Our findings enhance the understanding of sex roles in parental investment and highlight their importance as drivers of reproductive allocation.


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