Clay Model Reveals the Difference in Day and Night Predation Rates on Vietnam Warty Newt (Caudata: Salamandridae)

Abstract: Studying the relationships between predators and their prey is generally complex but provides valuable knowledge into the process of evolution. The clay model method is a technique that has been widely used to assess prey-predator interaction. In the study, we used clay models of the Vietnam warty newt (Paramesotriton deloustali) to evaluate its predator pressures in Tam Dao National Park (NP), northern Vietnam. We also employed camera traps to detect specific predators of the newt in nature. Our camera trap results showed that northern treeshrew (Tupaia belangeri), rats (Rattus sp.), and greater coucal (Centropus sinensis) are predators of the newt in Tam Dao NP. For the clay model experiment observed attacks on the head of clay models were triple those expected by chance, indicating that predators perceived the clay model as actual prey items. The proportions on the models predated upon differed in three habitat types: broadleaf evergreen forests, mixed broadleaf evergreen and bamboo forests, and bamboo forests. We also detected that the attacks on the models were mainly made by mammals. Attack rates at nighttime were three times higher than during the daytime.

[1]  S. Salvidio,et al.  Is the Northern Spectacled Salamander Salamandrina perspicillata aposematic? A preliminary test with clay models , 2021, Acta Herpetologica.

[2]  S. Lötters,et al.  The future of clay model studies , 2018, BMC Zoology.

[3]  Daniel T. Blumstein,et al.  Escaping From Predators: An Integrative View of Escape Decisions , 2018 .

[4]  Menna E. Jones,et al.  Biologically meaningful scents: a framework for understanding predator–prey research across disciplines , 2018, Biological reviews of the Cambridge Philosophical Society.

[5]  X. Santos,et al.  Aposematism and crypsis are not enough to explain dorsal polymorphism in the Iberian adder , 2017 .

[6]  A. Cordero-Rivera,et al.  Ethological and phenotypic divergence in insular fire salamanders: diurnal activity mediated by predation? , 2017, acta ethologica.

[7]  P. Bateman,et al.  A different kind of ecological modelling: the use of clay model organisms to explore predator–prey interactions in vertebrates , 2017 .

[8]  S. Salvidio,et al.  Safe caves and dangerous forests? Predation risk may contribute to salamander colonization of subterranean habitats , 2017, The Science of Nature.

[9]  Matthew T. McElroy Teasing apart crypsis and aposematism – evidence that disruptive coloration reduces predation on a noxious toad , 2016 .

[10]  M. Sparreboom Salamanders of the Old World: The Salamanders of Europe, Asia and Northern Africa , 2014 .

[11]  R. Saporito,et al.  A Test of Aposematism in the Dendrobatid Poison Frog Oophaga pumilio: The Importance of Movement in Clay Model Experiments , 2014 .

[12]  Yan Xie,et al.  Mammals of China , 2013 .

[13]  Kevin W Eliceiri,et al.  NIH Image to ImageJ: 25 years of image analysis , 2012, Nature Methods.

[14]  K. Mochida Combination of local selection pressures drives diversity in aposematic signals , 2011, Evolutionary Ecology.

[15]  R. Apfelbach,et al.  The effects of predator odors in mammalian prey species: A review of field and laboratory studies , 2005, Neuroscience & Biobehavioral Reviews.

[16]  N. Canteras,et al.  Defensive behavior , 2005, Neuroscience & Biobehavioral Reviews.

[17]  J. Mappes,et al.  Significance of the dorsal zigzag pattern of Vipera latastei gaditana against avian predators , 2005 .

[18]  T. Caro,et al.  Antipredator Defenses in Birds and Mammals , 2006 .

[19]  Shawn R. Kuchta Experimental Support for Aposematic Coloration in the Salamander Ensatina eschscholtzii xanthoptica: Implications for Mimicry of Pacific Newts , 2005, Copeia.

[20]  S. Mangan,et al.  Richness, Abundance, and Habitat Relations of Rodents in the Lang Bian Mountains of Southern Viet Nam , 1999 .

[21]  J. Bowmaker Evolution of colour vision in vertebrates , 1998, Eye.

[22]  E. Brodie DIFFERENTIAL AVOIDANCE OF CORAL SNAKE BANDED PATTERNS BY FREE‐RANGING AVIAN PREDATORS IN COSTA RICA , 1993, Evolution; international journal of organic evolution.

[23]  Alan A. Berryman,et al.  The Orgins and Evolution of Predator‐Prey Theory , 1992 .

[24]  K. Heckmann,et al.  Interspecific Morphogens Regulating Prey-Predator Relationships in Protozoa , 1985, Science.

[25]  B. G. Naylor The frontosquamosal arch in newts as a defence against predators , 1978 .

[26]  Á.,et al.  The effecT of PainT Marking on PredaTion risk in WesTern fence Lizards : a TesT Using cLay ModeLs , 2019 .

[27]  Jianping Jiang,et al.  Paramesotriton longliensis (Longli Warty Newt).Defensive behavior. , 2014 .

[28]  D. Adams,et al.  PREDATOR PERCEPTION OF BATESIAN MIMICRY AND CONSPICUOUSNESS IN A SALAMANDER , 2014 .

[29]  D. Hocking,et al.  Amphibian Contributions to Ecosystem Services , 2014 .

[30]  D. Adams,et al.  Predator perception of Batesian mimicry and conspicuousness in a salamander. , 2014, Evolution; international journal of organic evolution.

[31]  D. Gesch,et al.  Global multi-resolution terrain elevation data 2010 (GMTED2010) , 2011 .

[32]  C. Francis,et al.  A field guide to the mammals of South-East Asia , 2008 .

[33]  K. Wells The Ecology and Behavior of Amphibians , 2007 .

[34]  L. Heaney Small mammal diversity along elevational gradients in the Philippines: an assessment of patterns and hypotheses , 2001 .