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Predation and ingestion of a viviparous lizard (Zootoca vivipara) by the common wall lizard (Podarcis muralis) in England

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44 Herpetological Bullen 152 (2020)
The common wall lizard (Podarcis muralis) is a small-medium
sized lacerd that aains a snout to vent length (SVL) of
about 7.5 cm and varies considerably in colour or paern. Its
diet includes a wide range of invertebrates and small lizards
including its own young (Speybroeck et al., 2016). The species
ranges widely in connental Europe but has been introduced
into the Netherlands, Germany and Britain (Speybroeck et al.,
2016). Common wall lizards are thought to impact the nave
viviparous lizard (Zootoca vivipara) through compeon and
displacement (Mole, 2010) but this has yet to be quaned.
The viviparous lizard is a parcularly cold tolerant species
occupying a wide range of habitats across an expansive range
that extends from Ireland to Japan but absent from much of
southern Europe (Speybroeck et al., 2016). They too vary in
colour but oen tend to be brown, with females possessing a
dorsal stripe and the males a brightly coloured belly (Beebee
& Griths, 2000). Viviparous lizards are the smallest and
most widespread lizard species in the Brish Isles but their
populaons are declining for a variety of reasons (Beebee
& Griths, 2000). They prefer open habitats that are
undisturbed and have exposure to the sun such as railway
embankments, clis and heathland (Inns, 2011). This can lead
to them coming into direct contact with P. muralis.
The common wall lizard has numerous established
populaons in England (Quayle & Noble, 2000) and Wales.
One of the most well-studied is at Boscombe Clis in Dorset
(SW England) (Gleed-Owen, 2004; Mole, 2010). Using genec
analysis this populaon of P. muralis was found to originate
from either France or Italy (Michaelides et al., 2015), whereas
the nearby Seacombe populaon, which happens to be
closest to the sighng described here, was found to be of
Venean origin (Michaelides et al., 2015).
At 15:19 h on 13 May 2020 an adult P. muralis was
observed by PS capturing and ingesng an adult Z. vivipara
among boulders and foliage in Winspit Quarry, Dorset (GPS:
50° 35’05.5” N 2°01’ 59.1” W). The Z. vivipara was grasped
just behind the front legs (Fig. 1) before the whole lizard
was swallowed head-rst in its enrety. The process lasted
approximately 5 minutes, with P. muralis ingesng Z. vivipara
in stages with pauses of about 30 seconds at a me, returning
to a rock in direct sunlight to complete ingeson aer having
been briey disturbed by a passer-by.
To our knowledge this is the rst observaon of P.
muralis feeding on Z. vivipara although this behaviour is
consistent with the known habit of this species to eat small
lizards. It would seem that P. muralis is not only a potenal
competor of the viviparous lizard but it is also a predator.
Besides compeon and predaon common wall lizards may
potenally threaten viviparous lizard populaons through
transfer of pathogens or parasites although this aspect has
sll to be invesgated.
REFERENCES
Beebee, T. J. C. & Griths, R. A. (2000). Amphibians and
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London, HarperCollins. 270 pp.
Gleed-Owen, C.P. (2004). Green lizards and wall lizards on
Bournemouth clis. HerpetologicalBullen 88: 3-7.
Michaelides, S. N., While, G. M., Zajac, N. & Uller, T. (2015).
Widespread primary, but geographically restricted
secondary, human introducons of wall lizards, Podarcis
muralis. MolecularEcology 24: 2702-2714.
Mole, S. R. C. (2010). Changes in relave abundance of the
western green lizard Lacerta bilineata and the common
wall lizard Podarcis muralis introduced onto Boscombe
Clis, Dorset, UK. HerpetologicalBullen 114: 24-29.
Quayle, A. & Noble, M. (2000). The wall lizard in England.
BrishWildlife 12: 99-106.
Speybroeck, J., Beukema, W., Bok, B. & Van Der Voort, J.
(2016). Field Guide to the Amphibians and Reples of
BritainandEurope. London, Bloomsbury Publishing. 432
pp.
The Herpetological Bulletin 152, 2020: 44
Predaon and ingeson of a viviparous lizard (Zootoca vivipara) by
the common wall lizard (Podarcis muralis) in England
OLIVER THOMAS1*, STEVEN J. R. ALLAIN2 & PAUL SAGAR3
1Department of Biosciences, Swansea University, Swansea, SA2 8PP
2Cambridgeshire & Peterborough Amphibian and Reple Group
3Department of Polical Economy, King’s College London, London, WC2B 4BG
*Corresponding author e-mail: olliethomas444@gmail.com
hps://doi.org/10.33256/hb152.44
NATURAL HISTORY NOTE
Accepted:24May2020
Figure 1. An adult male common wall lizard (P. muralis) holding a
viviparous lizard (Z. vivipara) in its mouth shortly before consuming
the smaller lizard whole
... These accounts typically feature adult males consuming juveniles, however, one case of cannibalistic oophagy by an adult female has been reported (Lam 2022, Simović and Marković 2013, Zagar and Carretero 2012, Zagar et al. 2016. At least two accounts of saurophagy observed in wall lizards in Greece and the United Kingdom (Andriopoulos and Pafilis 2019, Thomas et al. 2020), and one field observation (G. Hanke, Royal BC Museum) near Prospect Lake, Vancouver Island, featured larger adults capturing and consuming smaller animals, suggesting that cannibalism is common in wall lizards. ...
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Introduced Common Wall Lizards (Podarcis murali) have steadily increased their range on Vancouver Island and other parts of coastal British Columbia, Canada since the 1970s. Without substantial observations of their feeding habits in this introduced range, a full assessment of the ecological impact of this species introduction is not possible. In this study, we provide qualitative observations on the diets of a large sample of urban dwelling Common Wall Lizards collected from a residential neighborhood in Victoria, British Columbia. Specimens were euthanized, dissected, and had their entire digestive tracts examined. Our observations showed a rich diet of invertebrates typical of wall lizards, with ants (Family Formicidae) as the most detected prey followed by beetles (Order Coleoptera), and earwigs (Order Dermaptera). Adults consumed approximately 30% more prey taxa than juveniles. We also found the remains of other wall lizards within ~5 % of adult guts, suggesting cannibalism or carcass scavenging. The results of this study provide additional information for assess- ing the potential impacts of wall lizard trophic interactions in their British Columbian range and can help orient future investigations focused on this introduced species.
... Like most Podarcis spp., it feeds mainly on arthropods (Bombi & Bologna, 2002), but also on gastropods, annelids, small vertebrates, and plants ( Barbault & Mou, 1986). It may also consume other lizards, when they are smaller than themselves, as evidenced by the predation of a Zootoca vivipara by an adult male P. muralis in Britain (Thomas et al., 2020). Here we report a case of cannibalism that took place in Boscombe cliffs, Dorset (50° 43'15.7" ...
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Establishing the introduction pathways of alien species is a fundamental task in invasion biology. The common wall lizard, Podarcis muralis, has been widely introduced outside of its native range in both Europe and North America, primarily through escaped pets or deliberate release of animals from captive or wild populations. Here we use Bayesian clustering, approximate Bayesian computation (ABC) methods and network analyses to reconstruct the origin and colonization history of 23 non-native populations of wall lizards in England. Our analyses show that established populations in southern England originate from at least nine separate sources of animals from native populations in France and Italy. Secondary introductions from previously established non-native populations were supported for eleven (47%) populations. In contrast to the primary introductions, secondary introductions were highly restricted geographically and appear to have occurred within a limited time frame rather than being increasingly common. Together, these data suggest that extant wall lizard populations in England are the result of isolated accidental and deliberate releases of imported animals since the 1970s, with only local translocation of animals from established non-native populations. Given that populations introduced as recently as 25 years ago show evidence of having adapted to cool climate, discouraging further translocations may be important to prevent more extensive establishment on the south coast of England. This article is protected by copyright. All rights reserved. This article is protected by copyright. All rights reserved.
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Introduced populations of Lacerta bilineata and Podarcis muralis were discovered on Boscombe cliffs in 2002. Since then both species have been breeding successfully. This investigation plotted their territory in 2007 and compared their population trends with that of the native Zootoca vivipara. Fifteen survey visits were undertaken between April and September 2007 during which time observations were made of 214 non-native and 44 native lizards. The two introduced species dominated the central area of the site with the native species found in substantial numbers only on the periphery. Comparison with previously collected survey data show that the relative abundance of non-native species has increased; between 2002 and 2007 P. muralis increased by 40% and L. bilineata by 36%; compared with Z. vivipara which declined by 75%. Sufficient habitat favourable to the introduced species means that there is the potential for unimpeded range expansion along the cliffs, which raises concern for a sand lizard Lacerta agilis population to the west of this site. Eradication of the non-native species may be impractical because they occur on a relatively inaccessible cliff face.
Amphibians and Reptiles: A Natural History of the British Herpetofauna
  • T J C Beebee
  • R A Griffiths
Beebee, T. J. C. & Griffiths, R. A. (2000). Amphibians and Reptiles: A Natural History of the British Herpetofauna. London, HarperCollins. 270 pp.
Green lizards and wall lizards on Bournemouth cliffs
  • C P Gleed-Owen
Gleed-Owen, C.P. (2004). Green lizards and wall lizards on Bournemouth cliffs. Herpetological Bulletin 88: 3-7.