Shared and unshared parental investment, parent-offspring conflict and brood size

1986 ◽  
Vol 34 (6) ◽  
pp. 1791-1804 ◽  
Author(s):  
John Lazarus ◽  
I.R. Inglis
2017 ◽  
Vol 247 ◽  
pp. 97-106 ◽  
Author(s):  
Maren N. Vitousek ◽  
Brittany R. Jenkins ◽  
Joanna K. Hubbard ◽  
Sara A. Kaiser ◽  
Rebecca J. Safran

Polar Biology ◽  
2021 ◽  
Vol 44 (10) ◽  
pp. 1961-1966
Author(s):  
Virginia Morandini ◽  
Javier Viñuela ◽  
Josabel Belliure ◽  
Miguel Ferrer

AbstractParent–offspring conflict theory predicts that offspring seek to prolong the parental care period, while parents strive to shorten it as much as possible. Transition to the crèche phase in penguins involves changes in the dynamic of parental investment in chicks, and thus may be modulated by interests that benefit parent or offspring. We explored parent–offspring interactions in the Chinstrap Penguin (Pygoscelis antarctica) to understand the influence such interactions would have on transition to crèche phase. We studied the effect of hatching date, nestling age, brood size, and nest location on parent–offspring interactions and the length of the guard phase. All behavioral variables related to nestling demands for parental investment increased as well as parental aggression towards their chicks, with increased nestling age. Brood size showed significant effects on both nestling and parental behavior. Hatching date was negatively correlated with the age at crèche. Consequently, the decision to leave the chicks unguarded seemed to be more based on the condition of adults rather than of the chicks. Given the short time available for breeding in Antarctica and that penguins are long-lived birds with several opportunities to breed, there may be conflicting selective factors between investment in feeding chicks versus extending the period of resource acquisition and storage prior to moult.


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.


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.


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.


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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