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Lunar phase as a cue for migrations to two species of explosive breeding amphibians—implications for conservation

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Abstract

In species with explosive breeding strategies, large numbers of individuals may congregate at a defined location for a very short period of time. Effective synchronisation in arrival at breeding sites is crucial to ensure mating success. Amphibians with explosive breeding strategies often congregate at ponds for only a few days or weeks a year. Previous research has shown that frogs and toads may use a variety of exogenous cues to initiate breeding migrations which include temperature, rainfall and lunar cues. Although the effects of temperature and rainfall on amphibians are widely studied and understood, the impacts of lunar phase are poorly known and vary by species and location. In this study, we examined the effects of lunar phase on the numbers of common toads (Bufo bufo) and common frogs (Rana temporaria) migrating to breeding ponds at 43 sites across the UK over 4 years. Our findings show that peak migration of both common toads and common frogs coincides with the waxing phase of the moon, peaking around the full moon. Temperature and rainfall also had an effect on peak migrations with the highest numbers of common toads and common frogs occurring on warm and damp evenings close to a full moon. Our results have implications for amphibian conservation initiatives such as ‘Toads on Roads’ as they will help inform conservationists on the most effective timing to help toads and frogs across roads.

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References

  • Akçakaya HR (2000) Viability analyses with habitat-based metapopulation models. Pop Ecol 42:45–53

    Google Scholar 

  • Andreone F, Giacoma C (1989) Breeding dynamics of Triturus carnifex at a pond in northwestern Italy (Amphibia, Urodela, Salamandridae). Holarc Ecol 12(3):219–223

    Google Scholar 

  • Arnfield H, Grant R, Monk C, Uller T (2012) Factors influencing the timing of spring migration in common toads (Bufo bufo). J Zool 288:112–118

    Google Scholar 

  • Baker BJ, Richardson JML (2006) The effect of artificial light on male breeding season behaviour in green frogs Rana clamitans melanota. Can J Zool 84:1528–1532

    Google Scholar 

  • Batschelet E (1981) Circular statistics in biology, vol 111. Academic Press, London

    Google Scholar 

  • Beebee TJC (1995) Amphibian breeding and climate change. Nature 374:219–220

    CAS  Google Scholar 

  • Beebee TJC (1996) Ecology and conservation of amphibians. Chapman and Hall, London

    Google Scholar 

  • Beebee TJC (2013) Effects of road mortality and mitigation measures on amphibian populations. Conserv Biol 2:657–668

    Google Scholar 

  • Beebee TJC, Griffiths RA (2000) Amphibians and reptiles. HarperCollins New Naturalist, London

    Google Scholar 

  • Bellis ED (1962) The influence of humidity on wood frog activity. Am Mid Nat 68:139–148

    Google Scholar 

  • Bevier CR (1997) Breeding activity and chorus tenure of two Neotropical hylid frogs. Herpetologica 53:297–311

    Google Scholar 

  • Blaustein AR, Belden LK, Olson DH, Green DM, Root TL, Kiesecker JM (2001) Amphibian breeding and climate change. Conserv Biol 15:1804–1809

    Google Scholar 

  • Bryne PG, Roberts JD (2004) Intrasexual selection and group spawning in quacking frogs (Crinia georgiana). Behav Ecol 15:872–882

    Google Scholar 

  • Carrier JA, Beebee TJC (2003) Recent, substantial and unexplained declines of the common toad Bufo bufo in lowland England. Biol Conserv 111:395–399

    Google Scholar 

  • Carroll EA, Sparks TH, Collinson N, Beebee TJC (2009) Influence of temperature on the spatial distribution of first spawning dates of the common frog (Rana temporaria) in the UK. Glob Change Biol 15:467–473

    Google Scholar 

  • Church G (1961) The effects of seasonal and lunar changes on the breeding pattern of the edible Javanese frog. Rana cancrivora:215–233

  • Cogălniceanu D, Székely P, Székely D, Roşioru D, Băncilă RI, Miaud C (2013) When males are larger than females in ecthotherms: reproductive investment in the eastern Spadefoot toad Pelobates syriacus. Copeia 2013(4):699–706

    Google Scholar 

  • Degani G (2015) The habitats, burrowing behavior, physiology adaptation and life cycle of Spadefoot toads (Pelobates syriacus, Boettger, 1869) at the southern limit of its distribution in Israel. Open J Anim Sci 2015(5):249–257

    Google Scholar 

  • Duellman WE, Trueb L (1994) Biology of amphibians. John Hopkins University Press, Baltimore, MD

    Google Scholar 

  • Fahrig L, Pedlar JH, Pope SE, Taylor PD, Wegner JF (1995) Effect of road traffic on amphibian density. Biol Conserv 73:177–182

    Google Scholar 

  • Fitzgerald GJ, Bider JR (1972) Influence of moon phase and weather factors on locomotory activity in Bufo americanus. Oikos 25:338–340

    Google Scholar 

  • FitzGerald GJ, Bider JR (1974) Seasonal activity of the toad Bufo americanus in southern Quebec as revealed by a sand-transect technique. Can J Zool 52:1–5

    Google Scholar 

  • Froglife (2019) Facts and figures, https://www.froglife.org/what-we-do/toads-on-roads/facts-figures/, Accessed 20 Oct 2020

  • Gittins SP, Parker AG, Slater FM (1980) Population characteristics of the common toad (Bufo bufo) visiting a breeding site in mid-Wales. J Anim Ecol 49:161–173

    Google Scholar 

  • Glista DJ, DeVault TL, DeWoody JA (2008) Vertebrate road mortality predominantly impacts amphibians. Herp Conserv Biol 3:77–87

    Google Scholar 

  • Gottsberger B, Gruber E (2004) Temporal partitioning of reproductive activity in a Neotropical anuran community. J Trop Ecol 20:271–280

    Google Scholar 

  • Grant RA, Chadwick EA, Halliday T (2009) The lunar cycle: a cue for amphibian reproductive phenology? Anim Behav 78:349–357

    Google Scholar 

  • Grant R, Halliday T, Chadwick E (2012) Amphibians’ response to the lunar synodic cycle—a review of current knowledge, recommendations, and implications for conservation. Behav Ecol 24:53–62. https://doi.org/10.1093/beheco/ars135

    Article  Google Scholar 

  • Green T, Das E, Green DM (2016) Springtime emergence of overwintering toads, Anaxyrus fowleri, in relation to environmental factors. Copeia 104:393–401

    Google Scholar 

  • Greenberg CH, Tanner GW (2004) Breeding pond selection and movement patterns by eastern Spadefoot toads (Scaphiophus holbrookii) in relation to weather and ediaphic conditions. J Herp 38:569–577

    Google Scholar 

  • Heinzmann U (1970) Untersuchungen zur bio-akustik und ökologie der geburtshelferkröte, Alytes o. obstetricans (Laur.). Oecologia 5:19–55

    PubMed  Google Scholar 

  • Hels T, Buchwald E (2001) The effect of road kills on amphibian populations. Biol Conserv 99:331–340

    Google Scholar 

  • Henzi SP, Dyson ML, Piper SE, Passmore NE, Bishop P (1995) Chorus attendance by male and female painted reed frogs (Hyperolius marmoratus): environmental factors and selection pressures. Funct Ecol 9:485–491

    Google Scholar 

  • Hiert C, Moura MO (2010) Abiotic correlates of temporal variation of Hypsiboas leptolineatus (Amphibia: Hylidae). Zoologica 27:703–708

    Google Scholar 

  • Hussin AG (2007) Hypothesis testing of parameters for ordinary linear circular regression. J App Sci Res 3:185–188

    Google Scholar 

  • Jammalamadaka SR, SenGupta A (2001) Topics in circular statistics, volume 5. New York World Scientific, New York

    Google Scholar 

  • Johnson DH, Batie RD (2001) Surveys of calling amphibians in North Dakota. USGS Northern Prairie Wildlife Research Center 156. http://digitalcommons.unl.edu/usgsnpwrc/156. Accessed 27 Sept 2019

  • Kusano T, Inoue M (2008) Long-term trends toward earlier breeding of Japanese amphibians. J Herp 42:608–614

    Google Scholar 

  • Kusano T, Miura T, Terui S, Maruyama K (2015) Factors affecting the breeding activity of the Japanese common toad, Bufo japonicus formosus (Amphibia: Bufonidae) with special reference to the lunar cycle. Current Herp 34:101–111

    Google Scholar 

  • Landler L, Ruxton GD, Malkemper EP (2018) Circular data in biology: advice for effectively implementing statistical procedures. Behav Ecol Sociobiol 72:128

    PubMed  PubMed Central  Google Scholar 

  • Loman J, Madsen T (2010) Sex ratio of breeding common toads (Bufo bufo): influence of survival and skipped breeding. Amphibia-Reptilia 31:509–524

    Google Scholar 

  • Lovari S, Renzoni A, Fondi R (1976) The predatory habits of the barn owl (Tyto alba scopoli) in relation to the vegetation cover. Ital J Zool 43:173–191

    Google Scholar 

  • Marsh DM, Rand AS, Ryan MJ (2000) Effects of inter-pond distance on the breeding ecology of túngara frogs. Oecologia 122:505–513

    CAS  PubMed  Google Scholar 

  • Mazerolle MJ (2004) Amphibian road mortality in response to nightly variations in traffic intensity. Herpetologica 60:45–53

    Google Scholar 

  • Narayan EJ, Molinia FC, Christi KS, Morley CG, Cockrem JF (2010) Annual cycles of urinary reproductive steroid concentrations in wild and captive endangered Fijian ground frogs. Gen Comp Endocr 166:172–179

    CAS  PubMed  Google Scholar 

  • Olson DH (1989) Predation on breeding western toads (Bufo boreas). Copeia 1989:391–397

    Google Scholar 

  • Padro CP d A, Uetanabaro M, Haddad CFB (2005) Breeding activity patterns, reproductive modes, and habitat use by anurans (Amphibia) in a seasonal environment in Pantanal, Brazil. Amphibia-Reptilia 26:211–221

    Google Scholar 

  • Petrovan SP, Schmidt BR (2016) Volunteer conservation action data reveals large-scale and long-term negative population trends of a widespread amphibian, the common toad (Bufo bufo). PLoS One 11:e0161943. https://doi.org/10.1371/journal.pone.0161943

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Reading CJ (1998) The effect of winter temperatures on the timing of breeding activity in the common toad Bufo bufo. Oecologia 117:469–475

    CAS  PubMed  Google Scholar 

  • Reading CJ (2007) The effect of winter temperatures on the timing of breeding activity in the common toad, Bufo bufo. Oecologia 117:469–475

    Google Scholar 

  • Reading CJ, Clarke RT (1983) Male breeding behaviour and mate acquisition in the common toad, Bufo bufo. J Zool (London) 201:237–246

    Google Scholar 

  • Rodrigues DJ, Uetanabaro M, Lopes FS (2004) Reproductive strategies of Physalaemus nattereri (Steindachner, 1863) and P. albonotatus (Steindachner, 1864) at Serra da Bodoquena, state of Mato Grosso do Sul, Brazil. Spanish Herp Rev 18:63–73

    Google Scholar 

  • Ryan MJ, Tuttle MD, Taft LK (1981) The costs and benefits of frog chorusing behaviour. Behav Ecol Sociobiol 8:273–278

    Google Scholar 

  • Scott AW, Pithart D, Adamson JK (2008) Long-term United Kingdom trends in the breeding phenology of the common frog, Rana temporaria. J Herp 42:89–96

    Google Scholar 

  • SenGupta A, Ugwuowo FI (2006) Asymmetric circular-linear multivariate regression models with applications to environmental data. Env Ecol Stat 13:299–309

    Google Scholar 

  • Sinsch U (1987) Orientation behaviour of toads (Bufo bufo) displaced from the breeding site. J Comp Physiol 161:715–727

    CAS  Google Scholar 

  • Sinsch U (1988) Seasonal changes in the migratory behaviour of the toad Bufo bufo: direction and magnitude of movement. Oecologia 76:390–398

    PubMed  Google Scholar 

  • Tomašević N, Cvetković D, Aleksić I, Crnobrnja-Isailović J (2007) Effect of climatic conditions on post-hibernation body condition and reproductive traits of Bufo bufo females. Arch Biol Sci Belgrade 59:51–52

    Google Scholar 

  • Trenham PC, Koenig WD, Mossman MJ, Stark SL, Jagger LA (2003) Regional dynamics of wetland-breeding frogs and toads: turnover and synchrony. Ecol Appl 13:1522–1532

    Google Scholar 

  • Vaira M (2005) Annual variation of breeding patterns of the toad, Melanophryniscus rubriventris (Vellard, 1947). Amphibia-Reptilia 26:193–199

    Google Scholar 

  • Verrell P, Halliday T (1985) Reproductive dynamics of a population of smooth newts, Triturus vulgaris, in southern England. Herpetologica 41:386–395

    Google Scholar 

  • Walther G, Post E, Convey P, Menzel A, Parmesan C, Beebee TJC, Fromentin J, Hoegh-Guldberg O, Bairlein F (2002) Ecological responses to recent climate change. Nature 416:389–395

    CAS  PubMed  Google Scholar 

  • Wells KD (2007) The ecology and behavior of amphibians. University of Chicago Press, Chicago

    Google Scholar 

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Acknowledgements

The authors would like to dedicate this manuscript to the late Professor Tim Halliday (1945–2019), in gratitude for supervision and support of the PhDs of LJ and RG. LJ carried out this research in part due to funding from the John Ellerman Foundation and Esmée Fairbairn Foundation. We would like to thank the many toads on roads volunteers who have helped toads across the roads at all the study sites and sending data to Froglife. In particular, we would like to thank Chris Monk and John Heasor in providing valuable information on toad patrols. Thanks are also due to Ajoy Mukhopadhyay for his help with the numerical analysis of the data.

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Correspondence to Laurence E. Jarvis.

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Jarvis, L.E., Grant, R.A. & SenGupta, A. Lunar phase as a cue for migrations to two species of explosive breeding amphibians—implications for conservation. Eur J Wildl Res 67, 11 (2021). https://doi.org/10.1007/s10344-020-01453-3

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