List of international per-reviewed publications

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2019

[46] BAŠKIERA, S. & GVOŽDÍK, L. 2019. Repeatability of thermal reaction norms for spontaneous locomotor activity in juvenile newts. J. Therm. Biol. 80: 126-132. Link

2018

2017

[41] JANČA, M. & GVOŽDÍK, L. 2017. Costly neighbours: Heterospecific competitive interactions increase metabolic rates in dominant species. Sci. Rep. 7: 5177. Pdf

[40] GVOŽDÍK, L. & KRISTÍN, P. 2017. Economic thermoregulatory response explains mismatch between thermal physiology and behavior in newts. J. Exp. Biol. 220: 1106-1111. Pdf

[39] STAROSTOVÁ, Z., GVOŽDÍK, L. & KRATOCHVÍL, L. 2017. An energetic perspective on tissue regeneration: The costs of tail autotomy in growing geckos. Comp. Biochem. Physiol. A 206: 82-86. Pdf

2016

[38] PODHAJSKÝ, L. & GVOŽDÍK, L. 2016. Variation in winter metabolic reduction between sympatric amphibians. Comp. Biochem. Physiol. A 201: 110-114. Pdf

[37] TOUFAROVÁ, E. & GVOŽDÍK, L. 2016. Do female newts modify thermoregulatory behavior to manipulate egg size? J. Therm. Biol. 57: 72-77. Pdf

[36] KRISTÍN, P. & GVOŽDÍK, L. 2016. Influence of surrounding medium on metabolic rates in alpine newts, Ichthyosaura alpestris, during aquatic phase. J. Herpetol. 50: 145-148. Pdf

2015

[35] GVOŽDÍK, L & SMOLINSKÝ, R. 2015. Body size, swimming speed, or thermal sensitivity? Predator-imposed selection on amphibian larvae. BMC Evol. Biol. 15: 238. Link

[34] PIASEČNÁ, K., PONČOVÁ, A., TEJEDO, M. & GVOŽDÍK, L. 2015. Thermoregulatory strategies in an aquatic ectotherm from thermally-constrained habitats: an evaluation of current approaches. J. Therm. Biol. 52: 97-107. Pdf

[33] BALOGOVÁ, M. & GVOŽDÍK, L. 2015. Can newts cope with the heat? Disparate thermoregulatory strategies of two sympatric species in water. PLoS ONE 10: e0128155. Link

[32] GVOŽDÍK, L. 2015. Mismatch between ectotherm thermal preferenda and optima for swimming: a test of the evolutionary pace hypothesis. Evol. Biol. 42: 137-145. Pdf

2014

[31] KRISTÍN, P. & GVOŽDÍK, L. 2014b. Individual variation in amphibian metabolic rates during overwintering: implications for a warming world. J. Zool. 294: 99–103. Pdf

[30] KRISTÍN, P. & GVOŽDÍK, L. 2014a. Aquatic-to-terrestrial habitat shift reduces energy expenditure in newts. J. Exp. Zool. A 321:183–188. Pdf

[29] POLČÁK, D. & GVOŽDÍK, L. 2014. Should I stay or should I go? The influence of temperature and sex on predator-induced responses in newts. Anim. Behav. 89: 79–84. Pdf

[28] SMOLINSKÝ, R. & GVOŽDÍK, L. 2014. Effect of temperature extremes on the spatial dynamics of predator–prey interactions: A case study with dragonfly nymphs and newt larvae.  J. Therm. Biol. 39: 12-16. Pdf

2013

[27] GVOŽDÍK, L., ČERNICKÁ, E. & VAN DAMME, R. 2013. Predator-prey interactions shape thermal patch use in a newt larvae-dragonfly nymph model. PLoS ONE 8: e6507. Link

[26] SMOLINSKÝ, R. & GVOŽDÍK, L. 2013. Does developmental acclimatization reduce the susceptibility to predation in newt larvae? Biol. J. Linn. Soc. 108: 109–115.Pdf

2012

[25] GVOŽDÍK, L. 2012a. Plasticity of preferred body temperatures as means of coping with climate change? Biol. Lett. 8: 262–265.Pdf

[24] GVOŽDÍK, L. 2012b. Metabolic costs of hybridization in newts. Folia Zool. 61: 197–201.Pdf

[23] KRISTÍN, P. & GVOŽDÍK, L. 2012. Influence of respirometry methods on intraspecific variation in standard metabolic rates in newts. Comp. Biochem. Physiol. A 163: 147–151.Pdf

[22] MAREK, V. & GVOŽDÍK, L. 2012. The insensitivity of thermal preferences to various thermal gradient profiles in newts. J. Ethol. 30: 35–41.Pdf

[21] SMOLINSKÝ, R. & GVOŽDÍK, L. 2012a. Interactive influence of biotic and abiotic cues on the plasticity of preferred body temperatures in a predator–prey system. Oecologia 170: 47–55.Pdf

2011

[20] HADAMOVÁ, M. & GVOŽDÍK, L. 2011. Seasonal acclimation of preferred body temperatures improves the opportunity for thermoregulation in newts. Physiol. Biochem. Zool. 84: 166–174.Pdf

[19] KURDÍKOVÁ, V., SMOLINSKÝ, R. & GVOŽDÍK, L. 2011. Mothers matter too. Benefits of temperature oviposition preferences in newts. PLoS ONE 6: e23842.Link

2010

[18] DVOŘÁK, J. & GVOŽDÍK, L. 2010. Adaptive accuracy of temperature oviposition preferences in newts. Evol. Ecol. 24: 1115–1127.Pdf

[17] ŠAMAJOVÁ, P. & GVOŽDÍK, L. 2010. Inaccurate or disparate temperature cues? Seasonal acclimation of terrestrial and aquatic locomotor capacity in newts. Funct. Ecol. 24: 1023–1030.Pdf

2009

[16] DVOŘÁK, J.& GVOŽDÍK, L. 2009. Oviposition preferences in newts: does temperature matter? Ethology 115: 533–539.Pdf

[15] MĚRÁKOVÁ, E. & GVOŽDÍK, L. 2009. Thermal acclimation of swimming performance in newt larvae: the influence of diel temperature fluctuations during embryogenesis. Funct. Ecol. 23: 989–995.Pdf

[14] SMOLINSKÝ, R. & GVOŽDÍK, L. 2009. The ontogenetic shift in thermoregulatory behaviour of newt larvae: testing the 'enemy-free temperatures' hypothesis. J. Zool. 279: 180–186.Pdf

[13] ŠAMAJOVÁ, P. & GVOŽDÍK, L. 2009. The influence of temperature on diving behaviour in the alpine newt, Triturus alpestris. J. Therm. Biol. 34: 401–405.Pdf

2008

[12] GVOŽDÍK, L.& VAN DAMME, R. 2008. The evolution of thermal performance curves in semiaquatic newts: thermal specialists on land and thermal generalists in water? J. Therm. Biol. 33: 395–405.Pdf

2007

[11] GVOŽDÍK, L., PUKY, M. & ŠUGERKOVÁ, M. 2007. Acclimation is beneficial at extreme test temperatures in the Danube crested newt, Triturus dobrogicus (Caudata, Salamandridae). Biol. J. Linn. Soc. 90: 627–636.Pdf

[10] VINŠÁLKOVÁ, T. & GVOŽDÍK, L. 2007. Mismatch between temperature preferences and morphology in F1 hybrid newts (Triturus carnifex × T. dobrogicus). J. Therm. Biol. 32: 433–439.Pdf

2006

[9] GVOŽDÍK, L. & VAN DAMME, R. 2006. Triturus newts defy the running-swimming dilemma. Evolution 60: 2110–2121.Pdf

2005

[8] GVOŽDÍK, L. 2005. Does reproduction influence temperature preferences in newts? Can. J. Zool. 83: 1038–1044.Pdf

2003

[7] GVOŽDÍK L. 2003. Postprandial thermophily in the Danube crested newt, Triturus dobrogicus. J. Therm. Biol. 28: 545–550.Pdf

[6] GVOŽDÍK L. & VAN DAMME R. 2003. Evolutionary maintenance of sexual dimorphism in head size in the lizard Zootoca vivipara: a test of two hypotheses. J. Zool. 259: 7–13.Pdf

2002

[5] GVOŽDÍK L. 2002. To heat or to save time? Thermoregulation in the lizard, Zootoca vivipara (Squamata: Lacertidae) in different thermal environments along an altitudinal gradient. Can. J. Zool. 80: 479–492.Pdf

2001

[4] GVOŽDÍK L. & CASTILLA A.M. 2001. A comparative study of preferred body temperatures and critical thermal tolerance limits among populations of Zootoca vivipara (Squamata: Lacertidae) along an altitudinal gradient. J. Herpetol. 35: 486–492.Pdf

2000

[3] GVOŽDÍK L. 2000. Intrapopulation variation in injury frequencies in the sand lizard, Lacerta agilis (Squamata: Lacertidae). Biológia (Bratislava) 55: 557–561.Pdf

1999

[2] GVOŽDÍK L. 1999. Colour polymorphism in a population of the common lizard, Zootoca vivipara (Squamata: Lacertidae). Folia Zool. 48:131–136.Pdf

1998

[1] GVOŽDÍK L. & BOUKAL M. 1998. Sexual dimorphism and intersexual niche overlap in the sand lizard, Lacerta agilis (Squamata: Lacertidae). Folia Zool. 47: 189–195.Pdf