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BARBOSA et al.
environments (Gonzalez-Candia, 2023; Santos et al.,
2024; Silva et al., 2024). In natural conditions, records
of thanatosis resulting from predation interactions are
scarce in the literature. Therefore, records of these
interactions are essential to evaluate the effectiveness
of the strategy in nature.
Leptodactylus comprises 84 species, with 61
occurring in Brazil (Segalla et al., 2021; Frost, 2024).
Many defensive behaviors are known for the genus
(e.g. Toledo et al., 2005; Sales et al., 2015; Costa &
Trevelin, 2020), including those that exhibit thanatosis,
show an adaptability that enhances their survival in
various environments by reducing predation risk
(Santiago, 2021).
The Patagonian green racer Philodryas
patagoniensis (Girard, 1858) has a generalist diet that
includes arachnids, small mammals, birds, fishes,
reptiles, and amphibians (Hartmann & Marques, 2005;
Quintela & Loebmann, 2019; Chuliver & Scanferla,
2024). Among amphibians, the family Leptodactylidae
constitutes a significant portion of their diet,
representing 13% of the total documented prey items
(Machado-Filho, 2015).
On February 13, 2020, an adult P. patagoniensis
(~1 m total length) was observed attempting to prey on
an individual of the Leptodactylus aff vastus in a
restinga environment within the Barra do Rio
Mamanguape Environmental Protection Area, Rio
Tinto, north coast of Paraíba, northeast Brazil (6° 46'
42.32" S, 34° 55' 20.35" W; WGS 84; altitude 7 m). At
7:18 am, the snake started the predation attempt by
biting the amphibian abdomen, which emitted an
agonistic vocalization. After approximately 10 seconds,
the amphibian ceased vocalizing and displayed
thanatosis, at this point, we start recording, the snake
continues biting the amphibian's head for another 14
seconds.
While the amphibian remained in thanatosis, P.
patagoniensis bits the head region (Fig. 1A),
immobilizing it for approximately 15 seconds. The
snake then bitten to the left forelimb (Fig. 1B) for four
seconds, followed by an attempt to ingest the
amphibian from the lower limbs (two seconds), another
an attempt to ingest the amphibian head-first for three
seconds and a brief bite to the left forelimb (<one
second) And the frog did not stop the thanatosis
behavior. The snake then repositioned frog belly on the
back of the frog for nine seconds. Shortly thereafter, the
snake returned, biting the amphibian head region for 14
seconds, dragging its body for less than 1 meter, and
ultimately retreating in the opposite direction.
Despite its behavior of death-feigning, the frog, at
all times, presents movements in its vocal sac,
indicating continuous breathing and makes a discreet
movement of its legs when the snake passes over it
(Fig. 1C; see 1:01 min of the video), indicating that it
was alive throughout the entire process of attempted
predation. In the present study, the frog showed a slight
movement when the snake passed over it, shrinking its
legs and tilting its head slightly, adopting a potential
escape behavior (Ferreira et al., 2019), however, after
the movement, the amphibian returned to the
thanatosis posture. Apparently, breathing is not
impaired in the behavior of playing dead, given that the
amphibian remained breathing throughout the
predation attempt, which was also reported for
Pristimantes ramagii (unpublished data) and
Silverstoneia flotator (Klank et al., 2023).
The thanatosis behavior lasted one minute and 30
seconds (video: https://youtu.be/r-r1dqFwu6Q). After
the snake left, the recording was stopped, and
approximately 10 seconds later, the amphibian
resumed its normal posture and jumped toward the
sandbank.
Although snakes have been documented preying
on dead animals (Barbosa et al., 2022), active prey is
generally more susceptible to predation than inactive
prey (Macdonald, 1973). Anuran amphibians can
sustain thanatosis for up to five minutes, during which
they may camouflage with their surroundings or
release odorous secretions to enhance the illusion of
being dead (Toledo et al., 2011; Lourenço-de-Moraes
et al., 2016). However, this Leptodactylus remained
still, with only movements of the vocal sac, until the
snake moved away completely, resuming the jumping
position and leaving the site of the attempted predation.
We believe that the “cameraman” had no influence
on the snake's decision to leave, as he remained still,
away from the snake, following the process, only
zooming the camera in and out, where the snake
releases the frog and moves away calmly, not showing
signs of running away.
Our observation highlights the effectiveness of
thanatosis as an anti-predator strategy in
Leptodactylus under natural conditions. The event
underscores the significance of this behavior on the
individual's survival, contributing to the growing body of
knowledge on the death-feigning in anurans. Future
studies and the record of field observations like that,
could help to understand the prevalence and adaptive
advantages of thanatosis across different populations
and environmental contexts, further elucidating its role
in predator-prey dynamics and its connection with
amphibian respiration, whether the immobility of the
limbs would be more important than the total reduction
of respiration.
We thank Rafael de Brito Costa for the imagens and
video recordings and the Instituto Chico Mendes de
Conservação da Biodiversidade (ICMBIO) for the
collection permit (SISBIO nº 74327-1). VNB, EFS and
LNR thank the National Council for Scientific and
Technological Development (CAPES) for PhD
scholarship and master's scholarship (grant numbers
88887.713778/2022-00, 88887.935257/2024-00 and
88887.956872/2024-00).
Bol. Soc. Zool. Uruguay (2ª época). 2025. ISSN 2393-6940Vol. 34(2): e34.2.6