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The Greenland White-fronted Goose Anser albifrons flavirostris

The Greenland White-fronted Goose Anser albifrons flavirostris

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study of the behaviour of marked individuals. We<br />

can use capture-mark-recapture programmes to<br />

estimate survival, follow reproduction, measure<br />

rates of individual emigration/immigration from<br />

wintering sites and determine individual life-time<br />

reproductive success and dispersal patterns<br />

which offer insights into how changes at the<br />

population level are manifest. Such information<br />

is vital if we are to understand the changes at<br />

population level and determine how density affects<br />

the individual, in terms of recruitment and<br />

survival probabilities, with respect to individual<br />

quality. Since populations are composed of individuals<br />

of differing quality, it is important to be<br />

able to show how competitive ability, age, experience<br />

and social status of the individual affect<br />

food intake rates, store acquisition and ultimately<br />

fitness measures. <strong>Greenland</strong> <strong>White</strong>-<strong>fronted</strong> Geese<br />

are long lived and may take six or more years to<br />

enter breeding age classes. For this reason, it is<br />

increasingly important to mark a representative<br />

sample of individuals on a regular basis over<br />

many years, to generate resightings of individuals<br />

and contribute to life histories that establish<br />

asymmetry in dispersal, fecundity and survival<br />

with regard to specific behavioural traits. In particular,<br />

it is increasingly important to maintain a<br />

pool of marked birds to form the basis for studies<br />

of differences in nutrient acquisition throughout<br />

the annual cycle. <strong>The</strong>re have been no specific behavioural<br />

or energetic investigations relating to<br />

the effects of social status and age on access to<br />

best quality food patches, peck rate and general<br />

levels of nutrient and energy acquisition. <strong>The</strong> relatively<br />

large numbers of marked individuals in this<br />

population, together with their extreme site loyalty,<br />

offer exciting possibilities in this respect. It<br />

is not enough to suggest that dominance hierarchies<br />

potentially skew the ability of an individual<br />

to acquire body stores, there needs to be some<br />

direct evidence of how and why this is achieved.<br />

<strong>The</strong> lack of detailed information relating to geese<br />

from this population wintering away from Wexford<br />

is lamentable. Given the difference in demographic<br />

patterns between Wexford and Islay, it<br />

would be highly desirable to resume a programme<br />

of regular capture-mark-recapture of individuals<br />

on Islay, preferably through a programme<br />

of collar marking in parallel to those at<br />

Wexford. Catching throughout the season at other<br />

sites would generate data on seasonality of mass<br />

86<br />

changes at other resorts for comparison with the<br />

pattern from Wexford. We need to learn more<br />

about the habitat use and other factors affecting<br />

numbers at lesser winter resorts, especially those<br />

that give immediate concern for their well being.<br />

At present, we do not know if the declines at such<br />

sites are due to poor survival, low reproductive<br />

success, high emigration, low immigration or a<br />

combination of some or all of these factors. Again,<br />

it is important to establish the causes of these<br />

changes before it is possible to tackle the conservation<br />

challenge through implementation of management<br />

action.<br />

Finally, having identified the key elements that<br />

potentially influence survival rates and fecundity,<br />

it is essential to test these in the field to establish<br />

some level of causation. Is climate change driving<br />

the difference in reproductive output at Wexford<br />

and Islay? Both wintering aggregations are<br />

showing declines in individual female fecundity,<br />

but this is greater at Wexford, where the effect<br />

has been to cause an overall decline in numbers<br />

not attributable to increases in the balance of<br />

emigration/immigration, nor to changes in annual<br />

survival. Is this because of changes in habitat<br />

at Wexford, cooler summers on the more northerly<br />

breeding areas which Wexford birds tend to<br />

use, or a combination of these factors? We need<br />

simultaneous studies of reproductive output from<br />

different parts of the breeding grounds with respect<br />

to local meteorological conditions from a<br />

number of years to establish the trends and patterns<br />

in breeding success. This would provide a<br />

firmer platform for predictions of the effects of<br />

global climate change than is possible at present,<br />

and enable generation of population predictions<br />

for changing scenarios as global climate models<br />

improve. We also need to understand how density<br />

dependence is manifest through dominance<br />

hierarchies – what are the real costs and benefits<br />

to an individual (e.g. in terms of fat or protein<br />

accumulation rates) of being part of a large group,<br />

or situated at the bottom of the league of social<br />

status? We need to be able to quantify these relative<br />

costs and benefits before we can be in a position<br />

to understand the function of such status and<br />

the strength of its effect in terms of fitness consequences<br />

for individuals. Only by understanding<br />

the behaviour of the individual will we be in a<br />

position to predict the future behaviour of the<br />

entire population.

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