2001Journal of Applied EcologyRequires access

The interplay between culling and density‐dependence in the great cormorant: a modelling approach

Morten Frederiksen, Jean‐Dominique Lebreton, Thomas Bregnballe

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Abstract

Summary The population of great cormorantsPhalacrocorax carbo sinensisbreeding in northern Europe has increased from 5000 pairs around 1970 toc. 100 000 pairs in the late 1990s, leading to serious conflicts with fishery and aquaculture interests. Management action, including widespread culling, has been taken in several countries. Since 1990, presumed density‐dependent declines in demographic performance have appeared in cormorant populations. We employed an extended Leslie matrix model to study the interaction between culls and density‐dependence in regulating breeding and autumn population sizes, with emphasis on evaluating the effects of culling. During 1979–92, the breeding population of great cormorants in northern Europe increased by 18% year−1, in accordance with observed life‐cycle parameters before the appearance of density‐dependent declines. We modelled six scenarios with varying assumptions about the strength of density‐dependence in adult survival and the proportions of breeding cormorants. A series of cull estimates was also included. Scenarios with moderate or strong levels of density‐dependence provided predictions that fit the observed numbers of breeding pairs, whereas scenarios without density‐dependence in survival overestimated real population growth. The most well‐supported scenarios indicated that the effect of culls at the present level (1998–99: 17 000 cormorants shot) was limited (< 10% reduction at equilibrium). Increasing the annual cull to 30 000 still had a limited effect, whereas shooting 50 000 birds year−1led to population extinction within 20–40 years. Shooting a fixed proportion of the population exceeding a threshold, through density‐dependent culling, could eliminate differences among scenarios and stabilize the population. We conclude that culls probably have had a limited effect on cormorant populations, but if carried out in a density‐dependent way they could stabilize numbers near a desired level. However, a reduction in the number of cormorants may not lead to a similar reduction in conflicts, and actions to control damage rather than cormorant populations are likely to be more cost‐effective. If culling is to be continued, we recommend the adoption of an adaptive and co‐ordinated management strategy across Europe. We also advocate the need to account for density‐dependent mechanisms in general culling strategies.

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Summary The population of great cormorantsPhalacrocorax carbo sinensisbreeding in northern Europe has increased from 5000 pairs around 1970 toc. 100 000 pairs in the late 1990s, leading to serious conflicts with fishery and aquaculture interests. Management action, including widespread culling, has been taken in several countries. Since 1990, presumed density‐dependent declines in demographic performance have appeared in cormorant populations. We employed an extended Leslie matrix model to study the interaction between culls and density‐dependence in regulating breeding and autumn population sizes, with emphasis on evaluating the effects of culling. During 1979–92, the breeding population of great cormorants in northern Europe increased by 18% year−1, in accordance with observed life‐cycle parameters before the appearance of density‐dependent declines. We modelled six scenarios with varying assumptions about the strength of density‐dependence in adult survival and the proportions of breeding cormorants. A series of cull estimates was also included. Scenarios with moderate or strong levels of density‐dependence provided predictions that fit the observed numbers of breeding pairs, whereas scenarios without density‐dependence in survival overestimated real population growth. The most well‐supported scenarios indicated that the effect of culls at the present level (1998–99: 17 000 cormorants shot) was limited (< 10% reduction at equilibrium). Increasing the annual cull to 30 000 still had a limited effect, whereas shooting 50 000 birds year−1led to population extinction within 20–40 years. Shooting a fixed proportion of the population exceeding a threshold, through density‐dependent culling, could eliminate differences among scenarios and stabilize the population. We conclude that culls probably have had a limited effect on cormorant populations, but if carried out in a density‐dependent way they could stabilize numbers near a desired level. However, a reduction in the number of cormorants may not lead to a similar reduction in conflicts, and actions to control damage rather than cormorant populations are likely to be more cost‐effective. If culling is to be continued, we recommend the adoption of an adaptive and co‐ordinated management strategy across Europe. We also advocate the need to account for density‐dependent mechanisms in general culling strategies.

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Available abstract

Summary The population of great cormorantsPhalacrocorax carbo sinensisbreeding in northern Europe has increased from 5000 pairs around 1970 toc. 100 000 pairs in the late 1990s, leading to serious conflicts with fishery and aquaculture interests. Management action, including widespread culling, has been taken in several countries. Since 1990, presumed density‐dependent declines in demographic performance have appeared in cormorant populations. We employed an extended Leslie matrix model to study the interaction between culls and density‐dependence in regulating breeding and autumn population sizes, with emphasis on evaluating the effects of culling. During 1979–92, the breeding population of great cormorants in northern Europe increased by 18% year−1, in accordance with observed life‐cycle parameters before the appearance of density‐dependent declines. We modelled six scenarios with varying assumptions about the strength of density‐dependence in adult survival and the proportions of breeding cormorants. A series of cull estimates was also included. Scenarios with moderate or strong levels of density‐dependence provided predictions that fit the observed numbers of breeding pairs, whereas scenarios without density‐dependence in survival overestimated real population growth. The most well‐supported scenarios indicated that the effect of culls at the present level (1998–99: 17 000 cormorants shot) was limited (< 10% reduction at equilibrium). Increasing the annual cull to 30 000 still had a limited effect, whereas shooting 50 000 birds year−1led to population extinction within 20–40 years. Shooting a fixed proportion of the population exceeding a threshold, through density‐dependent culling, could eliminate differences among scenarios and stabilize the population. We conclude that culls probably have had a limited effect on cormorant populations, but if carried out in a density‐dependent way they could stabilize numbers near a desired level. However, a reduction in the number of cormorants may not lead to a similar reduction in conflicts, and actions to control damage rather than cormorant populations are likely to be more cost‐effective. If culling is to be continued, we recommend the adoption of an adaptive and co‐ordinated management strategy across Europe. We also advocate the need to account for density‐dependent mechanisms in general culling strategies.

Key concepts: Culling, Density dependence, Cormorant, Population density, Population, Leslie matrix, Vital rates, Population model

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