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Foraging Success of the Tropical Frog, Eleutherodactylus coqui: The Cost of Calling
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf00346717openalex-snapshot
Feeding ecology of thirteen syntopic species of anurans in a seasonal tropical environment
inferredcites →https://doi.org/10.1007/bf00685209openalex-snapshot
Energetics of vocalization by an anuran amphibian (Hyla versicolor)
inferredcites →https://doi.org/10.1016/s0003-3472(84)80278-xopenalex-snapshot
Male parental care and its adaptive significance in a neotropical frog
inferredcites →https://doi.org/10.1086/282602openalex-snapshot
Models of Optimal Size for Solitary Predators
inferredcites →https://doi.org/10.1086/283899openalex-snapshot
Bat Predation and Sexual Advertisement in a Neotropical Anuran
inferredcites →https://doi.org/10.1086/284042openalex-snapshot
Sexual Selection and Size Dimorphism in Anuran Amphibia
inferredcites →https://doi.org/10.1086/physzool.55.1.30158439openalex-snapshot
Oxygen Consumption during Resting, Calling, and Nest Building in the Frog Physalaemus Pustulosus
inferredcites →https://doi.org/10.1126/science.214.4521.677openalex-snapshot
Bat Predation and the Evolution of Frog Vocalizations in the Neotropics
inferredcites →https://doi.org/10.1126/science.6894203openalex-snapshot
Internal Fertilization in an Oviparous Frog
inferredcites →https://doi.org/10.2307/1443480openalex-snapshot
A Possible Prey-Call Window in Anuran Auditory Perception
inferredcites →https://doi.org/10.2307/1563065openalex-snapshot
Prey Availability, Consumption and Selection in the Cricket Frog, Acris crepitans (Amphibia, Anura, Hylidae)
inferredcites →https://doi.org/10.2307/1563741openalex-snapshot
Diet and Foraging Mode of Bufo marinus and Leptodactylus ocellatus
inferredcites →https://doi.org/10.2307/1937072openalex-snapshot
Behavioral Modification of Evaporative Water Loss by a Puerto Rican Frog
inferredcites →https://doi.org/10.2307/2309989openalex-snapshot
Introduction to Statistical Analysis.
inferredcites →https://doi.org/10.2307/2388132openalex-snapshot
Acoustical Location of Calling Frogs by Philander Opossums
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4809405openalex-extracted
The Jumping Performance of Two Eleutherodactylus Frogs: The Effect of Temperature
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Chorus participation by male bullfrogs, Rana catesbeiana: a test of the energetic constraint hypothesis
inferred← citeshttps://doi.org/10.1007/978-3-319-27721-9_3openalex-snapshot
Vocal Sound Production and Acoustic Communication in Amphibians and Reptiles
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Divergence in mate choice systems: does evolution play by rules?
inferred← citeshttps://doi.org/10.1007/bf00183479openalex-snapshot
Determinants of chorus tenure in barking treefrogs ( Hyla gratiosa )
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Growth rate and the cost of calling activity in male carpenter frogs, Rana virgatipes
inferred← citeshttps://doi.org/10.1007/bf00649512openalex-snapshot
Effects of prey size and foraging mode on the ontogenetic change in feeding niche ofColostethus stepheni (Anura: Dendrobatidae)
inferred← citeshttps://doi.org/10.1007/s002650050394openalex-snapshot
Utilization of energy substrates during calling activity in tropical frogs
inferred← citeshttps://doi.org/10.1007/s10530-011-0127-3openalex-snapshot
Coqui frog invasions change invertebrate communities in Hawaii
inferred← citeshttps://doi.org/10.1007/s10530-016-1232-0openalex-snapshot
Dietary overlap between the invasive coquí frog (Eleutherodactylus coqui) and the Hawaiian hoary bat (Lasiurus cinereus semotus) on the Island of Hawai’i
inferred← citeshttps://doi.org/10.1016/b978-0-12-374931-4.10006-9openalex-snapshot
Stress and Reproduction in Amphibians
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Stress and Reproduction in Amphibians
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CHAPTER BIBLIOGRAPHIES
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Stress and reproduction in amphibians
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Trophic niche of four sympatric direct-developing frogs (Anura: Strabomantidae) from Eastern Brazilian Amazonia
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The jumping performance of two Eleutherodactylus frog species: the effect of temperature
inferred← citeshttps://doi.org/10.1016/s0003-3472(05)80342-2openalex-snapshot
Mate choice in the neotropical frog, Eleutherodactylus coqui
inferred← citeshttps://doi.org/10.1016/s0003-3472(05)80373-2openalex-snapshot
Determinants of chorus participation and the effects of size, weight and competition on advertisement calling in the tungara frog, Physalaemus pustulosus (Leptodactylidae)
inferred← citeshttps://doi.org/10.1017/s0266467406003245openalex-snapshot
Ontogenetic and seasonal variation in the diets of a Costa Rican leaf-litter herpetofauna
inferred← citeshttps://doi.org/10.1023/a:1021284426383openalex-snapshot
Divergence in Mate Choice Systems: does Evolution Play by Rules?
inferred← citeshttps://doi.org/10.1080/00222930903015824openalex-snapshot
Sexual dimorphism, reproduction and diet of the casque-headed treefrogItapotihyla langsdorffii(Hylidae: Lophiohylini)
inferred← citeshttps://doi.org/10.1080/00222933.2017.1297504openalex-snapshot
Arboreality predicts Batrachochytrium dendrobatidis infection level in tropical direct-developing frogs
inferred← citeshttps://doi.org/10.1080/01650521.2015.1048613openalex-snapshot
Diet ofAdenomera thomei(Almeida and Angulo, 2006) (Anura: Leptodactylidae) from a rubber tree plantation in southern Bahia, Brazil
inferred← citeshttps://doi.org/10.1080/01650521.2018.1485313openalex-snapshot
Trophic ecology of twoPithecopusspecies (Anura: Phyllomedusidae) living in syntopy in southern Bahia, Brazil
inferred← citeshttps://doi.org/10.1086/physzool.65.1.30158244openalex-snapshot
Reproductive Energetics of the African Reed Frogs, Hyperolius viridiflavus and Hyperolius marmoratus
inferred← citeshttps://doi.org/10.1093/beheco/arad116openalex-snapshot
Inter- and intraspecific female behavioral plasticity drive temporal niche segregation in two Tribolium species
inferred← citeshttps://doi.org/10.1111/1365-2656.70282openalex-snapshot
Playing it safe at early life stages: Balancing energy allocations to maximize fitness under seasonal pathogen dynamics
inferred← citeshttps://doi.org/10.1111/aec.12959openalex-snapshot
A continental assessment of diurnality in frog calling behaviour
inferred← citeshttps://doi.org/10.1111/j.1366-9516.2005.00178.xopenalex-snapshot
Potential consequences of the coqui frog invasion in Hawaii
inferred← citeshttps://doi.org/10.1111/j.1439-0310.1992.tb00970.xopenalex-snapshot
Territoriality and Male Mating Success in the Dart‐poison Frog,Epipedobates femoralis(Dendrobatidae, Anura)
inferred← citeshttps://doi.org/10.1111/j.1469-7998.1996.tb05294.xopenalex-snapshot
Energetic constraints and steroid hormone correlates of male calling behaviour in the túngara frog
inferred← citeshttps://doi.org/10.1111/j.1469-7998.1996.tb05487.xopenalex-snapshot
The evolution of myrmecophagy and its correlates in poison frogs (Family Dendrobatidae)
inferred← citeshttps://doi.org/10.1139/cjz-2014-0320openalex-snapshot
Ontogenetic shifts in ambush-site selection of a sit-and-wait predator, the Chacoan Horned Frog (Ceratophrys cranwelli)
inferred← citeshttps://doi.org/10.11606/0031-1049.2017.57.07openalex-snapshot
Diet of Dendropsophus microcephalus and Scarthyla vigilans (Anura: Hylidae) at a locality in north-western Venezuela with notes on microhabitat occupation
inferred← citeshttps://doi.org/10.11606/issn.2316-9079.v7i2p109-119openalex-snapshot
Diet, microhabitat and time of activity in a Pristimantis (Anura, Strabomantidae) assemblage
inferred← citeshttps://doi.org/10.1163/156853804322992832openalex-snapshot
The effect of supplemental feeding on the territorial behavior of the green frog (Rana clamitans)
inferred← citeshttps://doi.org/10.1186/2193-1801-1-51openalex-snapshot
Alkaloids from single skins of the Argentinian toad Melanophryniscus rubriventris (ANURA, BUFONIDAE): An unexpected variability in alkaloid profiles and a profusion of new structures
inferred← citeshttps://doi.org/10.1186/s40850-022-00117-wopenalex-snapshot
Endurance rivalry and female choice jointly influence male mating success in the emerald treefrog (Zhangixalus prasinatus), a lek-chorusing anuran
inferred← citeshttps://doi.org/10.13128/acta_herpetol-3414openalex-snapshot
Feeding pattern and use of reproductive habitat of the Striped toad Rhinella crucifer (Anura: Bufonidae) from Southeastern Brazil
inferred← citeshttps://doi.org/10.1371/journal.pone.0201883openalex-snapshot
Foraging connections: Patterns of prey use linked to invasive predator diel movement
inferred← citeshttps://doi.org/10.15446/abc.v20n1.41153openalex-snapshot
DIET OF DIRECT-DEVELOPING FROGS (ANURA: CRAUGASTORIDAE: Pristimantis) FROM THE ANDES OF WESTERN COLOMBIA
inferred← citeshttps://doi.org/10.15446/caldasia.v48.120422openalex-snapshot
Comparación de la dieta y atributos corporales de poblaciones de Rheohyla miotympanum (Anura: Hylidae) en dos hábitats contrastantes en México
inferred← citeshttps://doi.org/10.1590/1676-0611-bn-2020-1098openalex-snapshot
Feeding habits of the Robber Frog Pristimantis paulodutrai (Bokermann, 1975) in northeastern Brazil
inferred← citeshttps://doi.org/10.1590/s0101-81751996000200002openalex-snapshot
Alimentação e variação sazonal na freqüência de capturas de anuros em duas localidades do Brasil central
inferred← citeshttps://doi.org/10.1590/s0101-81751998000200011openalex-snapshot
Food habits and ontogenetic diet shifts of the litter dwelling frog proceratophrys boiei (wied)
inferred← citeshttps://doi.org/10.1643/0045-8511(2001)001[1064:vimaci]2.0.co;2openalex-snapshot
Variation in Male Advertisement Calls in the Neotropical Frog Physalaemus enesefae
inferred← citeshttps://doi.org/10.1643/0045-8511(2003)003[0248:reaboa]2.0.co;2openalex-snapshot
Reproductive Energetics and Behavior of an Australian Myobatrachid Frog Crinia georgiana
inferred← citeshttps://doi.org/10.1643/0045-8511(2007)7[281:dotife]2.0.co;2openalex-snapshot
Diet of the Invasive Frog, Eleutherodactylus Coqui, in Hawaii
inferred← citeshttps://doi.org/10.1643/ce-08-036openalex-snapshot
Beastly Bondage: The Costs of Amplexus in Cane Toads (Bufo marinus)
inferred← citeshttps://doi.org/10.1655/0018-0831(2007)63[245:gattdo]2.0.co;2openalex-snapshot
GROWING APART TOGETHER: THE DEVELOPMENT OF CONTRASTING SEXUAL SIZE DIMORPHISMS IN SYMPATRIC SCELOPORUS LIZARDS
inferred← citeshttps://doi.org/10.1655/herpmonographs-d-11-00010openalex-snapshot
Breeding Dynamics, Diet, and Body Condition of the Hong Kong Newt (Paramesotriton hongkongensis)
inferred← citeshttps://doi.org/10.1670/0022-1511(2002)036[0193:pdoeci]2.0.co;2openalex-snapshot
Population Dynamics of Eleutherodactylus coqui in Cordillera Forest Reserves of Puerto Rico
inferred← citeshttps://doi.org/10.1670/14-103openalex-snapshot
Diet of the Nonnative Greenhouse Frog (Eleutherodactylus planirostris) in Maui, Hawaii
inferred← citeshttps://doi.org/10.1670/15-170openalex-snapshot
Temporal Foraging Patterns of Nonnative Coqui Frogs (Eleutherodactylus coqui) in Hawaii
inferred← citeshttps://doi.org/10.1670/30-04aopenalex-snapshot
Diet of Epipedobates flavopictus (Anura: Dendrobatidae) in a Neotropical Savanna
inferred← citeshttps://doi.org/10.17161/randa.v27i1.14436openalex-snapshot
Male movement patterns and bioacoustic activity of the Western Cuban Grassfrog, Eleutherodactylus varleyi (Anura: Eleutherodactylidae)
inferred← citeshttps://doi.org/10.22201/ib.20078706e.2020.91.2748openalex-snapshot
Dieta de la rana de invernadero Eleutherodactylus planirostris (Amphibia: Eleutherodactylidae) en la península de Yucatán, México
inferred← citeshttps://doi.org/10.2307/1446096openalex-snapshot
Vocalizations and the Defense of Retreat Sites by Male and Female Frogs, Eleutherodactylus coqui
inferred← citeshttps://doi.org/10.2307/1447755openalex-snapshot
Use of Metabolic Substrates in the Gray Treefrog Hyla versicolor. Implications for Calling Behavior
inferred← citeshttps://doi.org/10.2307/1564677openalex-snapshot
Reproductive Ecology of the Puerto Rican Frog Eleutherodactylus coqui
inferred← citeshttps://doi.org/10.2307/1564775openalex-snapshot
Diet of the Frog Eleutherodactylus johnstonei (Leptodactylidae) in Barbados, West Indies
inferred← citeshttps://doi.org/10.2307/1564995openalex-snapshot
Climate Driven Population Fluctuations in Rain Forest Frogs
inferred← citeshttps://doi.org/10.2984/049.063.0301openalex-snapshot
Biology and Impacts of Pacific Island Invasive Species. 5.Eleutherodactylus coqui, the Coqui Frog (Anura: Leptodactylidae)
inferred← citeshttps://doi.org/10.2994/057.005.0105openalex-snapshot
Diet of the Cane Toad in Different Vegetation Covers in the Productive Systems of the Colombian Coffee Region
inferred← citeshttps://doi.org/10.2994/sajh-d-20-00047.1openalex-snapshot
Diet, Density, Biomass, and Prey Consumption through Ontogeny of a Dominant Frog Species at Different Distances from Streams in a Tropical Rainforest
inferred← citeshttps://doi.org/10.2994/sajh-d-21-00035.1openalex-snapshot
Diet and Habitat Use of Proceratophrys ararype (Anura: Odontophrynidae), an Endemic Frog from the Chapada do Araripe, Northeastern Brazil
inferred← citeshttps://doi.org/10.31611/ch.76openalex-snapshot
Diet of a community of frogs in an agroecosystem in western Cuba
inferred← citeshttps://doi.org/10.31611/ch.85openalex-snapshot
Diet of juveniles and adults of the Cuban Giant Frog, Eleutherodactylus zeus (Anura: Eleutherodactylidae)
inferred← citeshttps://doi.org/10.3390/ijms241210174openalex-snapshot
Metabolic Adaption of Flexor Carpi Radialis to Amplexus Behavior in Asiatic Toads (Bufo gargarizans)
inferred← citeshttps://doi.org/10.5962/bhl.title.16167openalex-snapshot
Trophic ecology of a tropical anuran assemblage / by Jeffrey R. Parmelee.
inferred← citeshttps://doi.org/10.64628/aai.fqm4fq49uopenalex-snapshot
How young coquí frogs balance the competing demands of growth and fighting disease
inferred← citeshttps://doi.org/10.64628/aai.rjmgttkmnopenalex-snapshot
¿Cómo las ranitas coquí jóvenes equilibran las demandas de crecimiento y de combatir enfermedades?
inferred← citeshttps://doi.org/10.7287/peerj.4059v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Lowland extirpation of anuran populations on a tropical mountain (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.4059v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Lowland extirpation of anuran populations on a tropical mountain (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.4059v0.2/reviews/1openalex-snapshot
Peer Review #1 of "Lowland extirpation of anuran populations on a tropical mountain (v0.2)"
inferred← citeshttps://doi.org/10.7554/elife.73401openalex-snapshot
The big potential of the small frog Eleutherodactylus coqui
inferred← citeshttps://doi.org/10.7717/peerj.4059openalex-snapshot
Lowland extirpation of anuran populations on a tropical mountain
inferred← citeshttps://doi.org/10.7717/peerj.496openalex-snapshot
Eleutherodactylus frogs show frequency but no temporal partitioning: implications for the acoustic niche hypothesis
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