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Antarctic Science 25(6), 763–766 (2013) & Antarctic Science Ltd 2013 doi:10.1017/S0954102013000126
Observations of mice predation on dark-mantled sooty albatross and Atlantic yellow-nosed albatross chicks at Gough Island
R.J. CUTHBERT1, H. LOUW1,2, G. PARKER1,2, K. REXER-HUBER1,2 and P. VISSER1,2
1 Royal Society for the Protection of Birds, The Lodge, Sandy, Bedfordshire, SG19 2DL, UK
2 DST/NRF Centre of Excellence at the Percy FitzPatrick Institute, University of Cape Town, Rondebosch 7701, South Africa
Abstract: Introduced house mice Mus musculus L. have been discovered to be major predators of chicks of
the Tristan albatross Diomedea dabbenena L. and Atlantic petrel Pterodroma incerta Schlegel and to also
predate great shearwater Puffinus gravis O’Reilly chicks at Gough Island, and similar predatory behaviour
has been reported for house mice on Marion Island. Observations on Gough Island over three breeding
seasons of nesting Atlantic yellow-nosed albatrosses Thalassarche chlororhynchos Gmelin and dark-
mantled sooty albatross Phoebetria fusca Hilsenberg indicate that house mice are also preying on these two
species: the first records of mice preying upon summer-breeding albatross species on Gough Island.
Predation on these two albatross species appears to be relatively rare ( , 2% for the Atlantic yellow-nosed albatrosses) and ongoing monitoring is required to ascertain if the impact of mice is increasing.
Conservation actions to eradicate mice from Gough Island will be of benefit to these species and other
species that are being impacted by this invasive species.
Received 17 September 2012, accepted 7 December 2012, first published online 21 May 2013
Key words: conservation, invasive species, Mus musculus, Phoebetria fusca, Thalassarche chlororhynchos
Introduction
The impact of invasive mammalian predators on islands is
well known (Atkinson 1985, Jones et al. 2008) and invasive
species remain one of the key threats for the conservation of
many bird species (Butchart 2008, Hilton & Cuthbert 2010).
On Gough Island in the South Atlantic Ocean, introduced
house mice Mus musculus L. prey on the chicks of albatrosses
and burrowing petrels. To date mice have been reported
killing nestlings of three seabird species: the Critically
Endangered Tristan albatross Diomedea dabbenena L., the
Endangered Atlantic petrel Pterodroma incerta Schlegel, and
the Least Concern great shearwater Puffinus gravis O’Reilly
(Cuthbert & Hilton 2004, Wanless et al. 2007). Further
evidence indicates that eggs and chicks of the endemic and
Critically Endangered Gough bunting Rowettia goughensis
Clarke are also preyed upon by mice on the island (Cuthbert &
Hilton 2004, Ryan & Cuthbert 2008). For populations of
winter-breeding Tristan albatross and Atlantic petrel the
current levels of predation are unsustainable, with 65–80% of
chicks killed each season (Cuthbert 2004, Cuthbert et al.
2004, Wanless et al. 2012). There are further concerns
and growing evidence that all winter breeding petrels on
Gough are being affected by mice predation (Angel &
Cooper 2006, Cuthbert et al. 2013). In this paper we describe
observations of mice predation on chicks of the summer-
breeding Atlantic yellow-nosed albatross Thalassarche
chlororhynchos Gmelin and dark-mantled sooty albatross
Phoebetria fusca Hilsenberg, the first records of such attacks
on Gough Island for these two globally endangered species.
Study area and methods
Monitoring of Atlantic yellow-nosed albatrosses was
undertaken at a long-term study colony (Cuthbert et al.
2003) and three other sites that are part of a monitoring
programme for the species (Cuthbert & Sommer 2004).
These four areas held 277–300 breeding pairs in the
three seasons of study (2008/09, 2009/10 and 2010/11).
Monitoring of chicks was made on at least weekly intervals
at the long-term study colony from hatching until all chicks
had fledged, with visits to the three other areas after the
peak of egg laying, after hatching and shortly before
fledging. Dark-mantled sooty albatross monitoring was
conducted via scan counts of coastal and inland cliffs
(Cuthbert & Sommer 2004) that held 212–238 breeding
pairs during the three seasons, with further counts in late
December and mid-March of numbers of hatched and
fledging chicks. Around 50 nests and chicks were checked
during 2008/09 and 2009/10 from both coastal and inland
areas with monthly nest checks in the 2009/10 season.
Further incidental observations on sooty albatross chicks
were made during ongoing plant eradication work on the
island’s sea-cliffs.
Results
The fresh carcass of a sooty albatross chick was discovered
at a nest on 15 December 2008. The chick had round
open wounds to the skin of its belly and the abdominal
cavity was exposed with the intestines visible (Fig. 1).
763
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Other than the observed wounds, the chick was undamaged
and appeared to be in good body-condition, with a mass of
0.45 kg and internal fat deposits. Directly underneath the
chick and located within the chick’s nest was the entrance
to a mouse hole (Fig. 1). A second dead sooty albatross
chick was found during the same period and on the same
stretch of cliffs. The body of this chick was too
decomposed to assess patterns of wounds, although it was
clear that the skin had been removed from behind its neck.
Fledging success (number of fledging chicks/number of
hatched chicks) of sooty albatrosses during the three
seasons was 56% (n 5 87 hatched chicks), 69% (n 5 78)
and 46% (n 5 82) in the 2008/09, 2009/10 and 2010/11
seasons, with an overall mean of 57.1 ± 11.5%.
An Atlantic yellow-nosed albatross chick was found
dead on 15 January 2010. This chick had hatched on the
22 December and weighed 1.7 kg at the time of death. The
carcass was fresh with very few fly maggots and other
invertebrates present and no visible sign of decay. Wounds
were found on the lower belly, exposing the viscera (Fig. 2).
The nest mound had a mouse hole in the cup and a mouse
hole at the base of the pedestal, with a well-used track
leading to it (Fig. 2). This predated chick was one of
52 hatched chicks in the long-term study colony where
regular (more than twice weekly) checks were made in the
2009/10 season, suggesting mice preyed upon a minimum of
2% of chicks in this season. Fledging success of this species
was 53% (n 5 194 hatched chicks), 64% (n 5 201) and 82%
(n 5 175) in the 2008/09, 2009/10 and 2010/11 seasons,
respectively. However, there was considerable variation
between the four sites in rates of survival during the 2009/10
breeding season with a coefficient of variation (CV) of 0.631
in comparison to CVs of 0.101 and 0.115 in the other two
years (Table I). The high variation in the 2009/10 season was
due to one site with very low chick survival (Table I).
Inspection of a sample of Atlantic yellow-nosed albatross
nest mounds (n 5 86 at two of the four sites) in the 2009/10
season indicated that 34% of nests had mouse holes in them,
of which eight had holes into the nest cup.
Discussion
This is the first time that mice have been reported to prey
upon summer-breeding albatross species on Gough Island
and the first records, of which we are aware, of mouse
preying on Atlantic yellow-nosed albatross chicks and
second observation of mice attacks on sooty albatross
chicks (Jones & Ryan 2009). The wounds to the stomach
and rump, and exposed viscera were identical in both
location and character to wounds observed on Tristan
albatross and Atlantic petrel chicks attacked by mice on
Gough Island and to wounds on wandering albatross
Diomedea exulans L. and dark-mantled sooty albatross
chicks on Marion Island (Cuthbert & Hilton 2004, Wanless
et al. 2007, Jones & Ryan 2010). The apparent rarity or
absence of mice preying upon summer breeding species on
Gough Island led Angel & Cooper (2006) to conclude that
the impact of mice was likely to be low for summer-
breeders, in contrast to the situation for winter-breeders.
This appears to be the case for both the yellow-nosed and
sooty albatross on Gough Island, where, despite the
observed predation events, overall rates of chick survival
are relatively high and in the range previously recorded for
the species on Gough and other islands (Tickell 2000,
Cuthbert et al. 2003). However, it is apparent that on a local
scale mice may be detrimental, with only 7% of Atlantic
yellow-nosed albatross chicks surviving to fledge at one site.
It is also important to note that the scavenging behaviour of
sub-Antarctic skuas Catharactica antarctica Lesson and
southern giant petrels Macronectes giganteus Gmelin on
Gough Island means that without frequent nest checks many
chicks could have been consumed and ‘‘disappeared’’
leaving no evidence that they were originally preyed upon
Fig. 1. a. The carcass of a sooty albatross chick with wounds to
its belly and abdomen and exposed viscera, and b. location
of the mouse hole within the nest and beneath the carcass of
the chick.
764 R.J. CUTHBERT et al.
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by mice. Consequently, levels of mouse depredation of
sooty and yellow-nosed albatross chicks on Gough Island
could be higher than suggested by our observations.
House mice have been reported to prey on chicks of
passerines and small petrels in other studies (Fugler et al.
1987, Ainley et al. 1990, Campos & Granadeiro 1999,
Michelsen-Heath & Gaze 2007), however it is only on
Gough Island and on sub-Antarctic Marion Island (Jones &
Ryan 2010) that house mice are known to prey upon
chicks of albatross species. At both Marion Island and
Gough Island predation events appear to be associated with
house mice utilizing albatross nest mounds. Mice on sub-
Antarctic islands are known to utilize burrows in order to
provide a warmer microclimate and their burrows are
disproportionally found in wandering albatross nesting
mounds in comparison to other habitats (Avenant & Smith
2003). These authors attribute the high proportion of mice
burrows around albatross nests to the high densities of soil
macro-invertebrates in these manure enriched sites, as
macro-invertebrates are a preferred food item for house
mice (Gleeson & Van Rensburg 1982, Jones et al. 2003).
An unfortunate by-product of this site selection by house
mice is that it may have contributed to the predatory
behaviour of mice on Gough and Marion islands, as such
burrows will place mice directly underneath albatross
chicks where chicks are most vulnerable.
Given the evidence for mice preying on two additional
species, further monitoring of breeding success and causes
Fig. 2. a. The carcass of an Atlantic yellow-nosed albatross chick with wounds on the belly and exposed viscera, and b. location of the
mouse hole within the nest mound and entrance of the mouse hole at the base of the pedestal.
Table I. Values of fledging success of Atlantic yellow-nosed albatrosses on Gough Island with sample size of hatched chicks in parentheses for the four
monitored sites and three breeding seasons, with the overall mean, standard deviation (SD) and coefficient of variation (CV).
Season Site 1 Site 2 Site 3 Site 4 Mean ± SD CV
2008/09 50% (48) 44% (45) 54% (24) 58% (77) 51.8 ± 6.0% 11.5%
2009/10 86% (52) 8% (50) 56% (27) 89% (72) 59.7 ± 37.7% 63.1%
2010/11 84% (32) 81% (53) 67% (21) 81% (69) 78.3 ± 7.9% 10.1%
MOUSE PREDATION OF ALBATROSSES AT GOUGH ISLAND 765
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of nesting failure are warranted for these and other species
to determine if this behaviour is becoming more
widespread and of greater severity on Gough Island.
Proposed conservation management actions to eradicate
house mice from Gough Island in order to remove a key
threat to the Critically Endangered Gough bunting and
Tristan albatross and Endangered Atlantic petrel will have
further benefits in eliminating this cause of breeding failure
for the Endangered Atlantic yellow-nosed albatross and
dark-mantled sooty albatross.
Acknowledgements
We thank the South African National Antarctic
Programme, University of Cape Town and Royal Society
for the Protection of Birds for providing logistical support
in the field and the Tristan da Cunha Conservation
Department for granting permission to work on Gough
Island. Funding was provided by the UK Government’s
Overseas Territories Environment Programme (OTEP).
Thanks to M. Nysschens for assistance with albatross
monitoring. The constructive comments of the reviewers
are gratefully acknowledged.
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