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Weight loss, reproductive output, and the cost of reproduction in the common frog, Rana temporaria
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/bimj.4710220416openalex-snapshot
RIEDWYL, H.: Angewandte mathematische statistik in wissenschaft, administration und technik. eine einführung. 2. überarb. u. erw. aufl., verlag paul haupt, bern und stuttgart 1979. 244 s., 184 abb., dm 35,‐; fr. 32
inferredcites →https://doi.org/10.1002/jcp.1030450303openalex-snapshot
The respiratory metabolism of frogs as related to season
inferredcites →https://doi.org/10.1007/bf00300069openalex-snapshot
Lek organization and mating strategies in the bullfrog
inferredcites →https://doi.org/10.1007/bf00300564openalex-snapshot
Growth rate and the cost of calling activity in male carpenter frogs, Rana virgatipes
inferredcites →https://doi.org/10.1007/bf00346972openalex-snapshot
?Costs? of reproduction in reptiles
inferredcites →https://doi.org/10.1007/bf00377295openalex-snapshot
Developmental plasticity and maternal effects of reproductive characteristics in the frog, Bombina orientalis
inferredcites →https://doi.org/10.1007/bf00379404openalex-snapshot
Reduction in locomotor ability as a cost of reproduction in gravid snakes
inferredcites →https://doi.org/10.1016/0003-3472(78)90094-5openalex-snapshot
Territoriality in the green frog (Rana clamitans): Vocalizations and agonistic behaviour
inferredcites →https://doi.org/10.1016/0300-9629(74)90027-9openalex-snapshot
Seasonal and age variation in the metabolism of the common frog, Rana temporaria L. In Northern Finland
inferredcites →https://doi.org/10.1016/s0003-3472(82)80138-3openalex-snapshot
Sexual selection in Woodhouse's toad (Bufo woodhousei) I. Chorus organization
inferredcites →https://doi.org/10.1016/s0003-3472(86)80060-4openalex-snapshot
Male territoriality, fighting and assessment of fighting ability in the Australian frog Uperoleia rugosa
inferredcites →https://doi.org/10.1080/03036758.1986.10418172openalex-snapshot
Oxford Surveys in Evolutionary Biology, edited by R.Dawkins and M.Ridley. Oxford University Press; Volume 1, pp. 222; Volume 2, pp. 243; 1984, 1985. NZ$100 (approx.) each.
inferredcites →https://doi.org/10.1086/284042openalex-snapshot
Sexual Selection and Size Dimorphism in Anuran Amphibia
inferredcites →https://doi.org/10.1086/409052openalex-snapshot
Life-History Tactics: A Review of the Ideas
inferredcites →https://doi.org/10.1093/icb/23.1.25openalex-snapshot
Alternative Concepts of Reproductive Effort, Costs of Reproduction, and Selection in Life-History Evolution
inferredcites →https://doi.org/10.1111/j.1469-7998.1986.tb03613.xopenalex-snapshot
The reproductive output of frogs Rana temporaria (L.) with particular reference to body size and age
inferredcites →https://doi.org/10.1111/j.1469-7998.1988.tb02465.xopenalex-snapshot
Determination of growth and maturation in the common frog, Rana temporaria , by skeletochronology
inferredcites →https://doi.org/10.1163/156853889x00269openalex-snapshot
The breeding migration and mating system of a Swiss population of the common frog Rana temporaria
inferredcites →https://doi.org/10.1242/jeb.26.4.412openalex-snapshot
Seasonal Changes in Blood Sugar, Fat Body, Liver Glycogen, and Gonads in the Common Frog, Rana Temporaria
inferredcites →https://doi.org/10.1515/9781400820108openalex-snapshot
Adaptation and Natural Selection: A Critique of Some Current Evolutionary Thought
inferredcites →https://doi.org/10.2307/1446044openalex-snapshot
Demography and Life History of Two Species of Chorus Frogs (Anura: Hylidae) in South Carolina
inferredcites →https://doi.org/10.2307/1936211openalex-snapshot
Territoriality and Male Mating Success in the Green Frog (Rana Clamitans)
inferredcites →https://doi.org/10.2307/2409372openalex-snapshot
OXFORD SURVEYS IN EVOLUTIONARY BIOLOGY
inferredcites →https://doi.org/10.2307/3544698openalex-snapshot
Costs of Reproduction: An Evaluation of the Empirical Evidence
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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What do frog calls tell us about males? The advertisement call of Physalaemus albifrons (Amphibia: Leptodactylidae) in the Brazilian semiarid region does not reflect either gonadal investment or energy storage
inferred← citeshttps://doi.org/10.1002/1438-390x.12210openalex-snapshot
Assessing population dynamics and environmental influences of Balearic green toad in the Balearic Islands
inferred← citeshttps://doi.org/10.1006/anbe.1996.0056openalex-snapshot
Callers and satellites: chorus behaviour in anurans as a stochastic dynamic game
inferred← citeshttps://doi.org/10.1006/anbe.2001.1801openalex-snapshot
Chorus participation by male bullfrogs, Rana catesbeiana: a test of the energetic constraint hypothesis
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The effects of density, rainfall and environmental temperature on body condition and fecundity in the common toad, Bufo bufo
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Does testis weight decline towards the Subarctic? A case study on the common frog, Rana temporaria
inferred← citeshttps://doi.org/10.1007/s00265-011-1267-2openalex-snapshot
Allocation in reproduction is not tailored to the probable number of matings in common toad (Bufo bufo) males
inferred← citeshttps://doi.org/10.1007/s00265-012-1412-6openalex-snapshot
Don’t get the blues: conspicuous nuptial colouration of male moor frogs (Rana arvalis) supports visual mate recognition during scramble competition in large breeding aggregations
inferred← citeshttps://doi.org/10.1007/s00442-003-1390-5openalex-snapshot
Growth or reproduction? Resource allocation by female frogs Rana temporaria
inferred← citeshttps://doi.org/10.1007/s00442-016-3593-6openalex-snapshot
Land colonisation by fish is associated with predictable changes in life history
inferred← citeshttps://doi.org/10.1016/0003-3472(92)90065-hopenalex-snapshot
Large male mating advantage in natterjack toads, Bufo calamita: sexual selection or energetic constraints?
inferred← citeshttps://doi.org/10.1016/j.actao.2008.05.003openalex-snapshot
Reproductive effort and the egg number vs. size trade-off in Physalaemus frogs (Anura: Leiuperidae)
inferred← citeshttps://doi.org/10.1016/j.actao.2009.06.012openalex-snapshot
Incidence of climate on common frog breeding: Long-term and short-term changes
inferred← citeshttps://doi.org/10.1016/j.cbpa.2025.111873openalex-snapshot
Fasting elicits immune modulation and leukocyte redistribution in bullfrogs (Lithobates catesbeianus)
inferred← citeshttps://doi.org/10.1016/j.ijppaw.2026.101243openalex-snapshot
Seasonal dynamic and individual determinants of Amphibiocystidium sp. infection in the palmate newt during the aquatic breeding season
inferred← citeshttps://doi.org/10.1016/j.jtherbio.2015.02.006openalex-snapshot
Behavioural adaptations of Rana temporaria to cold climates
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2016.08.015openalex-snapshot
Resting-state brain networks revealed by granger causal connectivity in frogs
inferred← citeshttps://doi.org/10.1016/j.smallrumres.2016.10.014openalex-snapshot
Proximity to females alters circulating testosterone concentrations and body weight in male goats
inferred← citeshttps://doi.org/10.1021/acs.est.2c04896openalex-snapshot
Complex Life Histories Alter Patterns of Mercury Exposure and Accumulation in a Pond-Breeding Amphibian
inferred← citeshttps://doi.org/10.1034/j.1600-0706.2000.880320.xopenalex-snapshot
Costs of reproduction in male lizards, Sceloporus virgatus
inferred← citeshttps://doi.org/10.1038/s41598-019-48147-8openalex-snapshot
Enlarged Egg Size Increases Offspring Fitness of a Frog Species on the Zhoushan Archipelago of China
inferred← citeshttps://doi.org/10.1038/sj.hdy.6800961openalex-snapshot
Genetic variability predicts common frog (Rana temporaria) size at metamorphosis in the wild
inferred← citeshttps://doi.org/10.1071/rd14214openalex-snapshot
Frequency of exogenous hormone therapy impacts spermiation in male Fowler's toad (Bufo fowleri)
inferred← citeshttps://doi.org/10.1078/1617-1381-00011openalex-snapshot
Rana temporaria metamorph production and population dynamics in the field – Effects of tadpole density, predation and pond drying
inferred← citeshttps://doi.org/10.1080/00222933.2017.1355075openalex-snapshot
Not every drought is bad: quantifying reproductive effort in the harlequin frogAtelopus laetissimus(Anura: Bufonidae)
inferred← citeshttps://doi.org/10.1080/02705060.2014.982725openalex-snapshot
Life-history costs of reproductive behaviors in a wetland-breeding amphibian
inferred← citeshttps://doi.org/10.1093/beheco/art024openalex-snapshot
Condition-dependent signaling and adoption of mating tactics in an amphibian with energetic displays
inferred← citeshttps://doi.org/10.1093/beheco/arx188openalex-snapshot
Temporal migration patterns and mating tactics influence size-assortative mating in Rana temporaria
inferred← citeshttps://doi.org/10.1093/biolinnean/blab040openalex-snapshot
The cost of breeding for male common toads
inferred← citeshttps://doi.org/10.1093/biolinnean/blae114openalex-snapshot
Terminal reproductive investment in male Eastern Gray Treefrogs (Dryophytes versicolor, Anura: Hylidae) is a marathon not a sprint
inferred← citeshttps://doi.org/10.1093/biolinnean/blx127openalex-snapshot
Geographical, climatic and biological constraints on age at sexual maturity in amphibians
inferred← citeshttps://doi.org/10.1093/biolinnean/blz119openalex-snapshot
Invasive toads adopt marked capital breeding when introduced to a cooler, more seasonal environment
inferred← citeshttps://doi.org/10.1093/conphys/coad101openalex-snapshot
The habitat quality paradox: loss of riparian forest cover leads to decreased risk of parasitism and improved body condition in an imperiled amphibian
inferred← citeshttps://doi.org/10.1111/btp.12437openalex-snapshot
Social facilitation is a better predictor of frog reproductive activity than environmental factors
inferred← citeshttps://doi.org/10.1111/eth.12961openalex-snapshot
Size‐dependent mating preference of the male fiddler crab Austruca perplexa
inferred← citeshttps://doi.org/10.1111/j.1365-2656.2010.01746.xopenalex-snapshot
Reduced predator species richness drives the body gigantism of a frog species on the Zhoushan Archipelago in China
inferred← citeshttps://doi.org/10.1111/j.1439-0469.2008.00504.xopenalex-snapshot
Bergmann’s rule in amphibians: combining demographic and ecological parameters to explain body size variation among populations in the common toadBufo bufo
inferred← citeshttps://doi.org/10.1111/j.1442-9993.1996.tb00622.xopenalex-snapshot
Decreased food intake in reproducing lizards: A fecundity‐dependent cost of reproduction?
inferred← citeshttps://doi.org/10.1111/j.1469-7998.1999.tb01060.xopenalex-snapshot
Variations in life‐history traits in the common frog Rana temporaria (Amphibia: Anura): a literature review and new data from the French Alps
inferred← citeshttps://doi.org/10.1111/j.1469-7998.2009.00552.xopenalex-snapshot
Insular shifts and trade‐offs in life‐history traits in pond frogs in the Zhoushan Archipelago, China
inferred← citeshttps://doi.org/10.1111/j.1600-0587.1996.tb00239.xopenalex-snapshot
Growth and body size in populations of mink frogs Rana septentrionalis from two latitudes
inferred← citeshttps://doi.org/10.1111/j.1600-0587.1996.tb01257.xopenalex-snapshot
Growth and body size in populations of mink frogs Rana septentrionalis from two latitudes
inferred← citeshttps://doi.org/10.1111/jav.01779openalex-snapshot
Experimental evidence of long‐term reproductive costs in a colonial nesting seabird
inferred← citeshttps://doi.org/10.1134/s1062359024701541openalex-snapshot
Variability in the Amount of Lymphatic Fluid in the Subcutaneous Sinuses of the Common Frog (Rana temporaria)
inferred← citeshttps://doi.org/10.1139/cjz-2012-0266openalex-snapshot
Relative influence of weather and season on anuran calling activity
inferred← citeshttps://doi.org/10.1139/z05-138openalex-snapshot
Life-history variation among populations of Canadian Toads in Alberta, Canada
inferred← citeshttps://doi.org/10.1139/z93-005openalex-snapshot
Plasticity of age at maturity between two neighbouring populations of the common frog (Rana temporaria L.)
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Growth and age of Alberta long-toed salamanders (Ambystoma macrodactylum krausei): a comparison of two methods of estimation
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Aspectos fisiológicos e ecológicos da estivação em Pleurodema diplolistris (Leiuperidae/Anura)
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Feeding habits of Lithobates megapoda (Anura: Ranidae), a threatened leopard frog used for human consumption, in Lake Chapala, Mexico
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Reproductive notes and larval development of Macrogenioglottus alipioi (Anura: Odontophrynidae) from the northern Atlantic forest
inferred← citeshttps://doi.org/10.11606/t.41.2016.tde-17102016-113321openalex-snapshot
Estratégias fisiológicas e comportamentais em anuros no semiárido: implicações sobre o balanço energético e hídrico
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Comparing three body condition indices in amphibians: a case study of yellow-bellied toad Bombina variegata
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Body size and life history traits of the fire salamander Salamandra salamandra from Poland
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The breeding migration and mating system of a Swiss population of the common frog Rana temporaria
inferred← citeshttps://doi.org/10.1163/1568539x-00003220openalex-snapshot
Male body size and parental relatedness but not nuptial colouration influence paternity success during scramble competition in Rana arvalis
inferred← citeshttps://doi.org/10.1163/157075403323012223openalex-snapshot
Frog farming: Investigation of biological and mechanical agents to increase the consumption of pelleted food by adult Rana temporaria
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Transcriptomic analysis of differentially expressed genes in the oviduct of Rhacophorus omeimontis provides insights into foam nest construction
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Sex-Related Differences in Metabolic Rate and Energy Reserves in Spring-Breeding Small-Mouthed Salamanders (Ambystoma texanum)
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inferred← citeshttps://doi.org/10.2108/zsj.19.343openalex-snapshot
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inferred← citeshttps://doi.org/10.2298/abs070351ptopenalex-snapshot
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inferred← citeshttps://doi.org/10.2307/1564830openalex-snapshot
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inferred← citeshttps://doi.org/10.2307/2389805openalex-snapshot
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inferred← citeshttps://doi.org/10.2307/3545621openalex-snapshot
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inferred← citeshttps://doi.org/10.26749/rstpp.139.29openalex-snapshot
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inferred← citeshttps://doi.org/10.3105/018.029.0103openalex-snapshot
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inferred← citeshttps://doi.org/10.3105/018.030.0108openalex-snapshot
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inferred← citeshttps://doi.org/10.3161/104.062.0401openalex-snapshot
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inferred← citeshttps://doi.org/10.31857/s0044513424050045openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ani15142132openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms241210174openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/life11101089openalex-snapshot
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inferred← citeshttps://doi.org/10.5358/hsj1972.16.2_29openalex-snapshot
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inferred← citeshttps://doi.org/10.5962/p.363989openalex-snapshot
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inferred← citeshttps://doi.org/10.70675/ddb893b5z06e5z4c85zaf2cz02af47776b7aopenalex-snapshot
Relations entre efficacité mitochondriale, balance oxydative et croissance des amphibiens
inferred← citeshttps://doi.org/10.7287/peerj.15179v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Captive breeding in the endangered alpine tree frog, Litoria verreauxii alpina (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.15179v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Captive breeding in the endangered alpine tree frog, Litoria verreauxii alpina (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.15179v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Captive breeding in the endangered alpine tree frog, Litoria verreauxii alpina (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.15179openalex-snapshot
Captive breeding in the endangered alpine tree frog, Litoria verreauxii alpina
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