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Coronella austriaca (smooth snake) - mortality after prey ingestion

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32 Herpetological Bullen 152 (2020)
The smooth snake is a medium sized European species that
feeds mainly on vertebrates. Reples and parcularly
lacerd lizards are considered as the main fracon of its
diet (Reading & Jofré, 2020). Legless reples are also
preyed upon by the smooth snake, but such cases seem to
be reported less frequently (Völkl et al., 2017). On 24 May
2019 a dead specimen of Coronella austriaca was found by
the roadside in Gogolin (opolskie vovoideship, south-west
Poland) with the tail of a slow-worm Anguis fragilis scking
out of its mouth. The snake had no external signs of being run
over by car or bicycle, had no wounds and also did not look
starved or weakened. X-ray examinaon was performed with
the use of computed radiography by Konika Minolta (Regius
Model 110s) and Siemens Polydoros LX 30 lamp (Fig. 1A).
Computed tomography was performed with the use of the
Siemens 16 slice CT scanner (Fig. 1B). The body length and
diameter of both the snake and slow worm were measured
and both were weighed.
Slow worms are not unusual prey items for smooth snakes,
so mortality following ingeson of a slow worm seems unlikely
and has never been reported previously. Greene (1983), who
explored the maximum limits of the rao prey mass/predator
mass (WR), showed that the liming rao for non-venomous
snakes is WR = 0.6. Based on body measurements of the
snake we collected (SVL = 340.0 cm; tail length = 76.0 cm;
head diameter = 12 mm; weight = 14 g) and the slow worm
(SVL = 86.0 cm; tail length = 97.0 cm; body diameter = 8 mm;
weight = 3 g) giving a WR of approximately 0.2 which is far
below the threshold suggested by Greene (1983). Thus the
smooth snake which we collected should have been fully
capable of swallowing prey of the size here recorded.
Indeed, larger prey items have been recorded as
swallowed and digested by smooth snakes (Juszczyk,
1987). However, the skin of Anguis fragilis has osteoderms
(Zylberberg & Castanet, 1985); these reduce skin exibility.
This could constrain the capacity of the snake to both
swallow such prey and to regurgitate it and could eventually
lead to suocaon, which is the proposed cause of death
here. Constraints of this kind might also result in lower size
limits for swallowing prey such as slow worms compared to
other prey types and explain why juvenile slow worms are
more commonly ingested by smooth snakes than adults
(Zimmermann, 1988).
Our observaon suggests that ingeson of legless prey
could carry the high cost of increased risk of mortality.
This, in turn could provide an addional explanaon of
why ophiophagy, including cannibalism, is relavely rarely
reported in snakes (Jackson et al., 2004) and why slow worms
seem not to avoid shelters already inhabited by potenal
predators, i.e. smooth snakes (Kolanek et al., 2019) or Vipera
berus (R.J. Hodges, personal communicaon).
REFERENCES
Greene, H. W. (1983). Dietary correlates of the origin and
radiaon of snakes. American Zoologist 23: 431-441.
Jackson, K., Kley, N. J. & Brainerd, E. L. (2004). How snakes
eat snakes: the biomechanical challenges of ophiophagy
for the California kingsnake, Lampropels getula californiae
(Serpentes: Colubridae). Zoology 107: 191-200.
The Herpetological Bulletin 152, 2020: 32-33
Coronella austriaca (smooth snake) - mortality aer prey ingeson
ALEKSANDRA KOLANEK1,2*, MONIKA PASTRYKIEWICZ3, WOJCIECH BORAWSKI4
& STANISŁAW BURY1,5
1NATRIX Herpetological Associaon, ul. Legnicka 65, 54-206 Wrocław, Poland
2Instute of Geography and Regional Development, University of Wrocław, pl. Uniwersytecki 1, 50-137 Wrocław, Poland
3Gogolin, Poland
4Department of Surgery, The Faculty of Veterinary Medicine, University of Environmental and Life Sciences, Wrocław, Poland
5Instute of Environmental Sciences, Jagiellonian University, Gronostajowa 7, 30-387 Kraków, Poland
*Corresponding author e-mail: aleksandra.kolanek@uwr.edu.pl
hps://doi.org/10.33256/hb152.3233
NATURAL HISTORY NOTE
Figure 1. A. Total body radiographic image in latero-lateral projecon
of a dead C. austriaca and its prey, and B. CT image of the same
animal, 3D image reconstrucon (60mAs i 130 kV, 0.6mm SD)
Herpetological Bullen 152 (2020) 33
Coronella austriaca mortality aer prey ingeson
Juszczyk, W. (1987). Płazy i Gady Krajowe. Część 3: Gady-
Replia. Państwowe Wydawnictwo Naukowe, Warszawa.
214 pp.
Kolanek, A., Bury, S., Turniak, E. & Szymanowski, M. (2019).
Age-dependent ulizaon of shelters and habitat in two
reple species with contrasng intraspecic interacons.
Animals 9: 995.
Reading, C. & Jofré, G. (2020). Smooth snake populaon
decline and its link with prey availability. Amphibia-
Replia 41: 43-48.
Völkl, W., Käsewieter, D. & Alfermann, D. (2017). Die
Schlingnaer: Eine Heimliche Jägeri. Lauren-Verlag,
Bielefeld 2003. 151 pp.
Zylberberg, L. & Castanet, J. (1985). New data on the structure
and the growth of the osteoderms in the reple Anguis
fragilis L.(Anguidae, Squamata). Journal of Morphology
186: 327-342.
Zimmermann, P. (1988). Die schlingnaer (Coronella
austriaca) im Weinberg “Hollstein” bei Freudenstein
(Enzkreis, Baden-Würemberg). Carolinea - Beiträge zur
naturkundlichen Forschung in Südwestdeutschland 46:
6-74.
Accepted: 2 April 2020
... There are few published records of P. apodus being preyed upon by snakes (e.g., Jovanović, 2009;Kukushkin, 2013;Stille and Stille, 2017;Plettenberg-Laing and Mee, 2020), but only Safaei-Mahroo et al. (2017) previously observed an adult being predated on. Kolanek et al. (2020) reported a smooth snake, Coronella austriaca (Laurenti, 1768), dying after ingesting a slow worm, Anguis fragilis, a member of the family Anguidae. The predating snake had an SVL of 34 cm whilst the prey item had a total length of 18.3 cm, therefore a length ratio of 1:0.5 was significantly smaller than the ratio recorded in the observation here of 1:0.9. ...
... The predating snake had an SVL of 34 cm whilst the prey item had a total length of 18.3 cm, therefore a length ratio of 1:0.5 was significantly smaller than the ratio recorded in the observation here of 1:0.9. The unsuccessful predation of the comparably smaller individual reported by Kolanek et al. (2020) further emphasises the magnitude of the predator-prey interaction reported here. ...
... Anguidae), but the information regarding these snakes' diet was obtained usually through analyses of their faeces or regurgitated stomach contents (GODDARD, 1984;READING and JOFRÉ, 2013;BROWN et al., 2014;JOFRE and READING, 2020;JOHANSEN et al., 2024). There is even a record of a smooth snake ending up dead after consuming a large slow worm (KOLANEK et al., 2020). However, regarding direct observations of C. austriaca consuming A. fragilis, only a photograph was found from Croatia (GUNTER), and a video from England (MELLOWSHIP, 2012). ...
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... The swallowing started when the western whip snake was likely dead. The absence of its corpse, as well as that of the predator itself, is a possible indication of the success of predation, since death can occur in cases of feeding on legless reptiles (Kolanek et al., 2020). ...
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Light and electron microscopy shows the osteoderms of Anguis fragilis to be small, flat disks located in the dermis along the adult trunk: microradiography established the extent of the mineralization. Each osteoderm coincides exactly with an epidermal fold forming the keratinized scales characteristic of the skin of reptiles. Sections perpendicular to the surface show two mineralized layers differing in histological and histochemical characteristics and in fine structure, although both contain collagen fibrils. The structure of each layer can be related to that of the surrounding dermis. The outer superficial layer located in the loose dermis contains few collagen bundles that form a discontinuous sheet at the upper surface of the osteoderms. This superficial layer appears to be constituted of units separated by furrows and is composed of woven fibered bone. The basal plate comprises stratified lamellae formed of parallel-oriented collagen fibrils; the fibrils of successive lamellae lie at right angles. The densely packed collagen fibrils of the basal plate are distributed similarly to those of the dense dermis within which it lies. This layer exhibits structural and histochemical characteristics of a lamellar bone. The presence of two different layers in the osteoderms of Anguis fragilis may reflect their mode of formation, which consists of the deposit of mineral crystals in the preexisting dermal tissue. This mineralization process, considered as a “metaplastic ossification,” may reflect the potentiality retained by the dermis of reptiles to form mineralized structures.
  • W Juszczyk
Juszczyk, W. (1987). Płazy i Gady Krajowe. Część 3: Gady-Reptilia. Państwowe Wydawnictwo Naukowe, Warszawa. 214 pp.
Die Schlingnatter: Eine Heimliche Jägeri
  • W Völkl
  • D Käsewieter
  • D Alfermann
Völkl, W., Käsewieter, D. & Alfermann, D. (2017). Die Schlingnatter: Eine Heimliche Jägeri. Laurenti-Verlag, Bielefeld 2003. 151 pp.
Die schlingnatter (Coronella austriaca) im Weinberg
  • P Zimmermann
Zimmermann, P. (1988). Die schlingnatter (Coronella austriaca) im Weinberg "Hollstein" bei Freudenstein (Enzkreis, Baden-Württemberg). Carolinea -Beiträge zur naturkundlichen Forschung in Südwestdeutschland 46: 6-74.