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Dispersal and alternative breeding site fidelity strategies in an amphibian

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ecy.1489openalex-snapshot
Does habitat unpredictability promote the evolution of a colonizer syndrome in amphibian metapopulations?
inferredcites →https://doi.org/10.1007/978-0-387-78151-8_36openalex-snapshot
The Stakes of Capture–Recapture Models with State Uncertainty
inferredcites →https://doi.org/10.1007/s00265-012-1433-1openalex-snapshot
Personality trait differences between mainland and island populations in the common frog (Rana temporaria)
inferredcites →https://doi.org/10.1007/s00265-017-2266-8openalex-snapshot
Geographic divergence in dispersal-related behaviour in cane toads from range-front versus range-core populations in Australia
inferredcites →https://doi.org/10.1007/s00442-006-0508-yopenalex-snapshot
Condition-dependent dispersal of a patchily distributed riparian ground beetle in response to disturbance
inferredcites →https://doi.org/10.1007/s004420050073openalex-snapshot
Choice of optimal oviposition sites by Hoplobatrachus occipitalis (Anura: Ranidae) in an unpredictable and patchy environment
inferredcites →https://doi.org/10.1007/s10531-012-0343-xopenalex-snapshot
Newt decline in Western Europe: highlights from relative distribution changes within guilds
inferredcites →https://doi.org/10.1016/j.anbehav.2008.12.022openalex-snapshot
The repeatability of behaviour: a meta-analysis
inferredcites →https://doi.org/10.1016/j.anbehav.2015.08.018openalex-snapshot
Amphibians forgo aquatic life in response to alien fish introduction
inferredcites →https://doi.org/10.1016/j.anbehav.2016.10.027openalex-snapshot
Habitat selection and reproduction of newts in networks of fish and fishless aquatic patches
inferredcites →https://doi.org/10.1016/j.anbehav.2016.11.002openalex-snapshot
Females trade off the uncertainty of breeding resource suitability with male quality during mate choice in an anuran
inferredcites →https://doi.org/10.1016/j.aquatox.2010.05.007openalex-snapshot
Cumulative effects of road de-icing salt on amphibian behavior
inferredcites →https://doi.org/10.1016/j.biocon.2013.10.020openalex-snapshot
Movement ecology of amphibians: A missing component for understanding population declines
inferredcites →https://doi.org/10.1016/j.cub.2011.07.030openalex-snapshot
The Origins and Evolution of Vertebrate Metamorphosis
inferredcites →https://doi.org/10.1016/j.ydbio.2007.03.021openalex-snapshot
Amphibian metamorphosis
inferredcites →https://doi.org/10.1016/s0003-3472(80)80103-5openalex-snapshot
Mating systems, philopatry and dispersal in birds and mammals
inferredcites →https://doi.org/10.1016/s0006-3207(03)00268-4openalex-snapshot
Delineation of terrestrial reserves for amphibians: post-breeding migrations of Italian crested newts (Triturus c. carnifex) at high altitude
inferredcites →https://doi.org/10.1017/s1464793104006645openalex-snapshot
Causes and consequences of animal dispersal strategies: relating individual behaviour to spatial dynamics
inferredcites →https://doi.org/10.1046/j.1365-2435.2000.00386.xopenalex-snapshot
Effects of age and size at metamorphosis on performance and metabolic rates of Southern Toad, Bufo terrestris, metamorphs
inferredcites →https://doi.org/10.1046/j.1365-2656.2003.00723.xopenalex-snapshot
Behavioural responses to habitat patch boundaries restrict dispersal and generate emigration–patch area relationships in fragmented landscapes
inferredcites →https://doi.org/10.1046/j.1365-2656.2003.00726.xopenalex-snapshot
Transience, dispersal and survival rates in newt patchy populations
inferredcites →https://doi.org/10.1046/j.1365-294x.2003.02016.xopenalex-snapshot
Fine‐scale genetic pattern and evidence for sex‐biased dispersal in the túngara frog, Physalaemus pustulosus
inferredcites →https://doi.org/10.1073/pnas.0706174104openalex-snapshot
Coupling of dispersal and aggression facilitates the rapid range expansion of a passerine bird
inferredcites →https://doi.org/10.1080/03949370.2016.1236040openalex-snapshot
Twenty years’ monitoring of a population of Italian crested newtsTriturus carnifex: strong site fidelity and shifting population structure in response to restoration
inferredcites →https://doi.org/10.1086/505765openalex-snapshot
Genetic and Maternal Determinants of Effective Dispersal: The Effect of Sire Genotype and Size at Birth in Side‐Blotched Lizards
inferredcites →https://doi.org/10.1086/688097openalex-snapshot
Evolution of Sex-Biased Dispersal
inferredcites →https://doi.org/10.1093/acprof:oso/9780199608898.001.0001openalex-snapshot
Dispersal Ecology and Evolution
inferredcites →https://doi.org/10.1093/acprof:oso/9780199608898.003.0001openalex-snapshot
Multicausality of dispersal: a review
inferredcites →https://doi.org/10.1093/acprof:oso/9780199608898.003.0004openalex-snapshot
Dispersal in invertebrates: influences on individual decisions
inferredcites →https://doi.org/10.1093/acprof:oso/9780199608898.003.0012openalex-snapshot
Dispersal syndromes in the common lizard: personality traits, information use, and context-dependent dispersal decisions
inferredcites →https://doi.org/10.1093/beheco/ars193openalex-snapshot
Individual and among-population variation in dispersal-related traits in Natterjack toads
inferredcites →https://doi.org/10.1098/rspb.2017.0176openalex-snapshot
The ‘male escape hypothesis’: sex-biased metamorphosis in response to climatic drivers in a facultatively paedomorphic amphibian
inferredcites →https://doi.org/10.1098/rstb.2010.0176openalex-snapshot
Personality-dependent dispersal: characterization, ontogeny and consequences for spatially structured populations
inferredcites →https://doi.org/10.1111/2041-210x.12717openalex-snapshot
Analysing movement behaviour and dynamic space‐use strategies among habitats using multi‐event capture‐recapture modelling
inferredcites →https://doi.org/10.1111/brv.12279openalex-snapshot
Behavioural synchronization of large‐scale animal movements – disperse alone, but migrate together?
inferredcites →https://doi.org/10.1111/ecog.02538openalex-snapshot
Evolution of dispersal strategies and dispersal syndromes in fragmented landscapes
inferredcites →https://doi.org/10.1111/ele.12728openalex-snapshot
Fast life history traits promote invasion success in amphibians and reptiles
inferredcites →https://doi.org/10.1111/eva.12049openalex-snapshot
Dispersal syndromes and the use of life‐histories to predict dispersal
inferredcites →https://doi.org/10.1111/gcb.13290openalex-snapshot
Demographic responses to weather fluctuations are context dependent in a long‐lived amphibian
inferredcites →https://doi.org/10.1111/gcb.13672openalex-snapshot
Life history tactics shape amphibians’ demographic responses to the North Atlantic Oscillation
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb00298.xopenalex-snapshot
PATTERNS OF NATURAL SELECTION ON SIZE AT METAMORPHOSIS IN WATER FROGS
inferredcites →https://doi.org/10.1111/j.0906-7590.2005.04042.xopenalex-snapshot
Dispersal and the metapopulation paradigm in amphibian ecology and conservation: are all amphibian populations metapopulations?
inferredcites →https://doi.org/10.1111/j.1365-2311.2012.01375.xopenalex-snapshot
Inter‐individual variation in movement: is there a mobility syndrome in the large white butterfly Pieris brassicae ?
inferredcites →https://doi.org/10.1111/j.1365-2427.2007.01793.xopenalex-snapshot
Foraging tactics in alternative heterochronic salamander morphs: trophic quality of ponds matters more than water permanency
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02596.xopenalex-snapshot
Microsatellite analyses reveal fine‐scale genetic structure in grey mouse lemurs (Microcebus murinus)
inferredcites →https://doi.org/10.1111/j.1365-294x.2010.04946.xopenalex-snapshot
Female philopatry and male-biased dispersal in a direct-developing salamander, Plethodon cinereus
inferredcites →https://doi.org/10.1111/j.1439-0310.1990.tb00407.xopenalex-snapshot
Courtship Display in a Natural Population of Crested Newts, Triturus cristatus
inferredcites →https://doi.org/10.1111/j.1461-0248.2008.01267.xopenalex-snapshot
Informed dispersal, heterogeneity in animal dispersal syndromes and the dynamics of spatially structured populations
inferredcites →https://doi.org/10.1111/j.1469-185x.2010.00172.xopenalex-snapshot
Evaluating the life-history trade-off between dispersal capability and reproduction in wing dimorphic insects: a meta-analysis
inferredcites →https://doi.org/10.1111/j.1469-185x.2011.00201.xopenalex-snapshot
Costs of dispersal
inferredcites →https://doi.org/10.1111/j.1523-1739.2001.00129.xopenalex-snapshot
Metapopulation Dynamics and Amphibian Conservation
inferredcites →https://doi.org/10.1111/j.1523-1739.2001.99200.xopenalex-snapshot
Habitat Matrix Effects on Pond Occupancy in Newts
inferredcites →https://doi.org/10.1111/j.1558-5646.1986.tb00568.xopenalex-snapshot
THE EVOLUTION OF WING DIMORPHISM IN INSECTS
inferredcites →https://doi.org/10.1111/j.1600-1706.2009.17882.xopenalex-snapshot
Capture–recapture models with heterogeneity to study survival senescence in the wild
inferredcites →https://doi.org/10.1139/z06-038openalex-snapshot
Oviposition-site selection by the toad Melanophryniscus rubriventris in an unpredictable environment in Argentina
inferredcites →https://doi.org/10.1139/z93-267openalex-snapshot
Variation in age structures in a subdivided population of Triturus cristatus
inferredcites →https://doi.org/10.1139/z94-241openalex-snapshot
Seasonal movement patterns in a subalpine population of the tiger salamander, Ambystoma tigrinum nebulosum
inferredcites →https://doi.org/10.1146/annurev.ecolsys.38.091206.095611openalex-snapshot
How Does It Feel to Be Like a Rolling Stone? Ten Questions About Dispersal Evolution
inferredcites →https://doi.org/10.1146/annurev.ento.42.1.207openalex-snapshot
PHYSIOLOGY AND ECOLOGY OF DISPERSAL POLYMORPHISM IN INSECTS
inferredcites →https://doi.org/10.1163/156853810790457821openalex-snapshot
Movements of Alpine newts (Mesotriton alpestris) between small aquatic habitats (ruts) during the breeding season
inferredcites →https://doi.org/10.1186/1742-9994-12-s1-s13openalex-snapshot
The maternal social environment shapes offspring growth, physiology, and behavioural phenotype in guinea pigs
inferredcites →https://doi.org/10.1186/s12983-015-0103-3openalex-snapshot
Linking habitat suitability to demography in a pond-breeding amphibian
inferredcites →https://doi.org/10.1371/journal.pone.0062727openalex-snapshot
Similar Local and Landscape Processes Affect Both a Common and a Rare Newt Species
inferredcites →https://doi.org/10.1577/m04-053.1openalex-snapshot
The Use of Two New Portable 12-mm PIT Tag Detectors to Track Small Fish in Shallow Streams
inferredcites →https://doi.org/10.1655/herpetologica-d-15-00072openalex-snapshot
Postbreeding Movements in Marbled Newts (Caudata, Salamandridae): A Comparative Radiotracking Study in Two Habitat Types
inferredcites →https://doi.org/10.1890/0012-9615(2003)073[0045:drscia]2.0.co;2openalex-snapshot
DOES REPRODUCTIVE SITE CHOICE IN A NEOTROPICAL FROG MIRROR VARIABLE RISKS FACING OFFSPRING?
inferredcites →https://doi.org/10.1890/0012-9658(2001)082[3519:sadaid]2.0.co;2openalex-snapshot
SPATIALLY AUTOCORRELATED DEMOGRAPHY AND INTERPOND DISPERSAL IN THE SALAMANDERAMBYSTOMA CALIFORNIENSE
inferredcites →https://doi.org/10.1890/09-0910.1openalex-snapshot
Life‐history evolution in range‐shifting populations
inferredcites →https://doi.org/10.1890/09-2016.1openalex-snapshot
Populations in small, ephemeral habitat patches may drive dynamics in a Daphnia magna metapopulation
inferredcites →https://doi.org/10.1890/11-0133.1openalex-snapshot
Life history benefits of residency in a partially migrating pond‐breeding amphibian
inferredcites →https://doi.org/10.1890/11-0892.1openalex-snapshot
From metamorphosis to maturity in complex life cycles: equal performance of different juvenile life history pathways
inferredcites →https://doi.org/10.1890/12-1999.1openalex-snapshot
Terrestrial distribution of pond‐breeding salamanders around an isolated wetland
inferredcites →https://doi.org/10.1890/13-1564.1openalex-snapshot
Estimating dispersal among numerous sites using capture–recapture data
inferredcites →https://doi.org/10.1890/15-0693.1openalex-snapshot
Contrasting patterns of environmental fluctuation contribute to divergent life histories among amphibian populations
inferredcites →https://doi.org/10.2193/2007-082openalex-snapshot
Differentiating Migration and Dispersal Processes for Pond‐Breeding Amphibians
inferredcites →https://doi.org/10.2307/1444758openalex-snapshot
Time and Energy Costs of Metamorphosis in the Indian Bullfrog Rana tigrina
inferredcites →https://doi.org/10.2307/1940580openalex-snapshot
Calling Site Choice by Hyla Chrysoscelis: Effect of Predators, Competitors, and Oviposition Sites
inferredcites →https://doi.org/10.2307/2680169openalex-snapshot
Spatially Autocorrelated Demography and Interpond Dispersal in the Salamander Ambystoma californiense
inferredcites →https://doi.org/10.2307/2937297openalex-snapshot
The Metapopulation Ecology of the Red‐Spotted Newt, Notophthalmus viridescens (Rafinesque)
inferredcites →https://doi.org/10.2307/3544901openalex-snapshot
Ecological Processes That Affect Populations in Complex Landscapes
inferredcites →https://doi.org/10.2307/3545205openalex-snapshot
Effects of Body Size and Parasite Infection on the Locomotory Performance of Juvenile Toads, Bufo bufo
inferredcites →https://doi.org/10.2307/3802723openalex-snapshot
Model Selection and Multimodel Inference: A Practical Information-Theoretic Approach
inferredcites →https://doi.org/10.3758/s13428-011-0058-zopenalex-snapshot
The use of visual and automatized behavioral markers to assess methodologies: a study case on PIT-tagging in the Alpine newt

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.3897/herpetozoa.37.e107986zenodo-depositor-declared
Three brown frog species in Denmark have different abilities to colonise new ponds
inferred← citeshttps://doi.org/10.1002/2688-8319.12310openalex-snapshot
Spatial prioritisation for crested newt conservation in Luxembourg: Insights from population genetics and species distribution modelling
inferred← citeshttps://doi.org/10.1002/eap.1909openalex-snapshot
Survival cost to relocation does not reduce population self‐sustainability in an amphibian
inferred← citeshttps://doi.org/10.1002/ece3.11480openalex-snapshot
Woodland caribou calving fidelity: Spatial location, habitat, or both?
inferred← citeshttps://doi.org/10.1002/ece3.4994openalex-snapshot
Sampling related individuals within ponds biases estimates of population structure in a pond‐breeding amphibian
inferred← citeshttps://doi.org/10.1002/ece3.9022openalex-snapshot
Evaluating the role of body size and habitat type in movement behavior in human‐dominated systems: A frog's eye view
inferred← citeshttps://doi.org/10.1002/ecs2.4345openalex-snapshot
Multistate model to estimate sex‐specific dispersal rates and distances for a wetland‐breeding amphibian population
inferred← citeshttps://doi.org/10.1002/ecy.2195openalex-snapshot
Estimating dispersal in spatiotemporally variable environments using multievent capture–recapture modeling
inferred← citeshttps://doi.org/10.1007/s00359-022-01584-9openalex-snapshot
The amphibian magnetic sense(s)
inferred← citeshttps://doi.org/10.1007/s00442-019-04362-8openalex-snapshot
The role of predation risk in metamorphosis versus behavioural avoidance: a sex-specific study in a facultative paedomorphic amphibian
inferred← citeshttps://doi.org/10.1007/s10344-025-01932-5openalex-snapshot
Occupancy analysis uncovers environmental factors contributing to road mortality of amphibians
inferred← citeshttps://doi.org/10.1007/s10530-020-02243-3openalex-snapshot
Spatio-temporal patterns of occupation and density by an invasive fish in streams
inferred← citeshttps://doi.org/10.1007/s10592-021-01335-4openalex-snapshot
Fine scale genetic structure in fire salamanders (Salamandra salamandra) along a rural-to-urban gradient
inferred← citeshttps://doi.org/10.1007/s10592-022-01437-7openalex-snapshot
Population structure and genetic diversity of the threatened pygmy newt Triturus pygmaeus in a network of natural and artificial ponds
inferred← citeshttps://doi.org/10.1007/s10592-023-01539-wopenalex-snapshot
The common ground in landscape effects on gene flow in two newt species in an agroecosystem
inferred← citeshttps://doi.org/10.1007/s10750-022-04888-8openalex-snapshot
Efficiency of aquatic PIT-tag telemetry, a powerful tool to improve monitoring and detection of marked individuals in pond environments
inferred← citeshttps://doi.org/10.1007/s10980-021-01297-5openalex-snapshot
Scale-dependent effects of terrestrial habitat on genetic variation in the great crested newt (Triturus cristatus)
inferred← citeshttps://doi.org/10.1007/s10980-023-01685-zopenalex-snapshot
Influence of landscape connectivity on newt’s response to a warmer climate
inferred← citeshttps://doi.org/10.1016/j.agee.2024.109049openalex-snapshot
Use of agricultural fields by Natterjack toads: Implications for pesticide exposure
inferred← citeshttps://doi.org/10.1016/j.anbehav.2019.01.026openalex-snapshot
Slow natal dispersal across a homogeneous landscape suggests the use of mixed movement behaviours during dispersal in the Darwin's frog
inferred← citeshttps://doi.org/10.1016/j.biocon.2019.05.028openalex-snapshot
Integrating amphibian movement studies across scales better informs conservation decisions
inferred← citeshttps://doi.org/10.1016/j.biocon.2020.108911openalex-snapshot
The upward elevational shifts of pond breeding amphibians following climate warming
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2026.120367openalex-snapshot
Microcystin-LR interferes with the intestinal remodeling during tadpole metamorphosis by disrupting thyroid hormone signaling pathways
inferred← citeshttps://doi.org/10.1016/j.gecco.2020.e01197openalex-snapshot
Soil moisture & roads influence the occurrence of frogs in Kathmandu Valley, Nepal
inferred← citeshttps://doi.org/10.1016/j.gecco.2024.e03194openalex-snapshot
Integrating fine-scale habitat suitability and hydrological structures to assess population connectivity for the Kaiser's mountain newt (Neurergus kaiseri) in southwest of Iran
inferred← citeshttps://doi.org/10.1016/j.heliyon.2023.e17241openalex-snapshot
Monitoring spatiotemporal impacts of changes in land surface temperature on near eastern fire salamander (Salamandra infraimmaculata) in the Middle East
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.167644openalex-snapshot
Waterborne exposure to microcystin-leucine arginine induces endocrine disruption and gonadal dysplasia of Pelophylax nigromaculatus tadpoles via the hypothalamic-pituitary-gonadal-liver axis
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.175917openalex-snapshot
Water availability and biological interactions shape amphibian abundance and diversity in Mediterranean temporary rivers
inferred← citeshttps://doi.org/10.1038/s41437-019-0221-3openalex-snapshot
MHC structuring and divergent allele advantage in a urodele amphibian: a hierarchical multi-scale approach
inferred← citeshttps://doi.org/10.1038/s41598-019-39251-wopenalex-snapshot
Personality-dependent breeding dispersal in rural but not urban burrowing owls
inferred← citeshttps://doi.org/10.1086/707862openalex-snapshot
Determinants and Consequences of Dispersal in Vertebrates with Complex Life Cycles: A Review of Pond-Breeding Amphibians
inferred← citeshttps://doi.org/10.1111/1365-2656.12926openalex-snapshot
Migratory plasticity is not ubiquitous among large herbivores
inferred← citeshttps://doi.org/10.1111/1365-2656.13208openalex-snapshot
Drivers of amphibian population dynamics and asynchrony at local and regional scales
inferred← citeshttps://doi.org/10.1111/1365-2656.13503openalex-snapshot
Informed breeding dispersal following stochastic changes to patch quality in a pond‐breeding amphibian
inferred← citeshttps://doi.org/10.1111/gcb.15766openalex-snapshot
Climate‐associated decline of body condition in a fossorial salamander
inferred← citeshttps://doi.org/10.1111/jzo.13137openalex-snapshot
Life on the beach: Movements and growth of a coastal amphibian vary with distance to the sea
inferred← citeshttps://doi.org/10.1111/jzs.12250openalex-snapshot
Genetic structure of lake and stream populations in a Pyrenean amphibian ( Calotriton asper ) reveals evolutionary significant units associated with paedomorphosis
inferred← citeshttps://doi.org/10.1111/mec.14848openalex-snapshot
Demographic and genetic approaches to study dispersal in wild animal populations: A methodological review
inferred← citeshttps://doi.org/10.1111/mec.15249openalex-snapshot
Comparative landscape genetics reveals the evolution of viviparity reduces genetic connectivity in fire salamanders
inferred← citeshttps://doi.org/10.1111/mec.15521openalex-snapshot
Multiple glacial refugia and contemporary dispersal shape the genetic structure of an endemic amphibian from the Pyrenees
inferred← citeshttps://doi.org/10.1111/mec.16114openalex-snapshot
Context‐dependent dispersal determines relatedness and genetic structure in a patchy amphibian population
inferred← citeshttps://doi.org/10.1111/oik.08951openalex-snapshot
Natal dispersal does not entail survival costs but is linked to breeding dispersal in a migratory shorebird, the southern dunlin Calidris alpina schinzii
inferred← citeshttps://doi.org/10.11160/bah.248openalex-snapshot
The importance of naturalized quarries as amphibian breeding sites: a case study in central Spain
inferred← citeshttps://doi.org/10.1163/15685381-bja10017openalex-snapshot
Movement patterns, maximum distances traveled and microhabitat selection of spadefoot toad tadpoles in temporary ponds
inferred← citeshttps://doi.org/10.1163/15685381-bja10081openalex-snapshot
Orientation and emigration of larval and juvenile amphibians: selected topics and hypotheses
inferred← citeshttps://doi.org/10.1186/s12862-021-01844-3openalex-snapshot
Dispersal and mating patterns determine the fate of naturally dispersed populations: evidence from Bombina orientalis
inferred← citeshttps://doi.org/10.21203/rs.3.rs-10471860/v1openalex-snapshot
Rivers, hybridisation, and range margins: drivers of genetic structure in the Danube crested newt in northern Pannonia
inferred← citeshttps://doi.org/10.3389/famrs.2023.1215723openalex-snapshot
Multiple introductions and human-aided dispersal of the UK’s most widespread non-native amphibian
inferred← citeshttps://doi.org/10.3389/fevo.2019.00155openalex-snapshot
Behavior in a Changing Landscape: Using Movement Ecology to Inform the Conservation of Pond-Breeding Amphibians
inferred← citeshttps://doi.org/10.3389/fevo.2022.813414openalex-snapshot
Early Development Drives Variation in Amphibian Vulnerability to Global Change
inferred← citeshttps://doi.org/10.3389/fevo.2023.1157297openalex-snapshot
Connectivity, land use, and fish presence influence smooth newt (Lissotriton vulgaris) occurrence and abundance in an urban landscape
inferred← citeshttps://doi.org/10.3390/d17050350openalex-snapshot
Correlation Between Individual Body Condition and Seasonal Activity in Buresch’s Crested Newt, Triturus ivanbureschi
inferred← citeshttps://doi.org/10.6084/m9.figshare.14746507openalex-snapshot
Additional file 1 of Dispersal and mating patterns determine the fate of naturally dispersed populations: evidence from Bombina orientalis
inferred← citeshttps://doi.org/10.70675/aac1908az3ab3z4926z8e94z0c3b3f389cf1openalex-snapshot
Étude de la perméabilité de la LGV Bretagne – Pays de la Loire (BPL) aux déplacements des amphibiens
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