Activity budgets of northern pintail hens: influence of brood size, brood age, and date

1985 ◽  
Vol 63 (9) ◽  
pp. 2114-2120 ◽  
Author(s):  
Shirley J. Rushforth Guinn ◽  
Bruce D. J. Batt
Keyword(s):  
Parental Care ◽  
Parental Investment ◽  
Brood Size ◽  
Class Ii ◽  
Class I ◽  
Time Budgets ◽  
Early Season ◽  
Northern Pintail ◽  
Brood Rearing ◽  
Maintenance Activities

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.

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.
Keyword(s):  
Sex Differences ◽  
Parental Care ◽  
Group Size ◽  
Parental Investment ◽  
Brood Size ◽  
Time Budget ◽  
Feeding Time ◽  
Anser Brachyrhynchus ◽  
Term Pair ◽  
Pink Footed Goose

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 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.
Keyword(s):  
Sex Differences ◽  
Parental Care ◽  
Group Size ◽  
Parental Investment ◽  
Brood Size ◽  
Time Budget ◽  
Feeding Time ◽  
Anser Brachyrhynchus ◽  
Term Pair ◽  
Pink Footed Goose

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.

scholarly journals Parental Care System and Brood Size Drive Sex Difference in Reproductive Allocation: An Experimental Study on Burying Beetles

2021 ◽  
Vol 9 ◽  
Author(s):  
Wenxia Wang ◽  
Long Ma ◽  
Maaike A. Versteegh ◽  
Hua Wu ◽  
Jan Komdeur
Keyword(s):  
Parental Care ◽  
Parental Investment ◽  
Brood Size ◽  
Life History Theory ◽  
Empirical Studies ◽  
Reproductive Allocation ◽  
Burying Beetle ◽  
Future Reproduction ◽  
The Impact ◽  
Care System

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.

Electron microscopy analysis of degenerating pancreatic ß cells in transgenic mice expressing the MHC Class I antigen Dd

1990 ◽  
Vol 48 (3) ◽  
pp. 548-549
Author(s):  
T. A. Stewart ◽  
D. Liggitt ◽  
S. Pitts ◽  
L. Martin ◽  
M. Siegel ◽  
...  
Keyword(s):  
Type I Diabetes ◽  
Disease Process ◽  
Class Ii ◽  
Class I ◽  
Type I ◽  
Aberrant Expression ◽  
Mhc Molecules ◽  
Endogenous Insulin ◽  
Class Ii Mhc ◽  
Ifn Γ

Insulin-dependant (Type I) diabetes mellitus (IDDM) is a metabolic disorder resulting from the lack of endogenous insulin secretion. The disease is thought to result from the autoimmune mediated destruction of the insulin producing ß cells within the islets of Langerhans. The disease process is probably triggered by environmental agents, e.g. virus or chemical toxins on a background of genetic susceptibility associated with particular alleles within the major histocompatiblity complex (MHC). The relation between IDDM and the MHC locus has been reinforced by the demonstration of both class I and class II MHC proteins on the surface of ß cells from newly diagnosed patients as well as mounting evidence that IDDM has an autoimmune pathogenesis. In 1984, a series of observations were used to advance a hypothesis, in which it was suggested that aberrant expression of class II MHC molecules, perhaps induced by gamma-interferon (IFN γ) could present self antigens and initiate an autoimmune disease. We have tested some aspects of this model and demonstrated that expression of IFN γ by pancreatic ß cells can initiate an inflammatory destruction of both the islets and pancreas and does lead to IDDM.

Pictish Horse Carvings

1991 ◽  
Vol 17 (1) ◽  
pp. 53-62
Author(s):  
Irene Hughson
Keyword(s):  
Class Ii ◽  
Class I ◽  
Early Historic Period ◽  
High Quality ◽  
Historic Period ◽  
Agricultural Economy ◽  
Different Types ◽  
Early Historic

Summary This paper examines the horse carvings to be found on Class I and Class II Pictish sculptured stones and considers their reliability as evidence of the sort of horses and ponies that would have existed in the Early Historic Period. An attempt is made to show that the availability in Britain of good sized, high quality riding horses during that period is not inconsistent with what is known of the development and distribution of different types of horses in pre-hislory. The importance of horses and ponies in Early Historic societies is stressed and inferences drawn about the agricultural economy that could support horses and the skilled specialists required to look after them.

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