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Environmental and Developmental Effects on External Gill Loss in the Red‐Eyed Tree Frog,Agalychnis callidryas
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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/ar.1090780202openalex-snapshot
Stages in the normal development of Rana pipiens I. External form
inferredcites →https://doi.org/10.1002/ar.1091120109openalex-snapshot
Pattern series of the first embryonary stages in Bufo arenarum
inferredcites →https://doi.org/10.1002/dvg.1020140508openalex-snapshot
Pleiotropic effects of the Cardiac‐lethal gene in the axolotl (Ambystoma mexicanum)
inferredcites →https://doi.org/10.1002/jez.1402140209openalex-snapshot
The environmental control of hatching in Fundulus heteroclitus
inferredcites →https://doi.org/10.1002/jmor.1051670303openalex-snapshot
Embryonic stages of Gastrotheca riobambae (fowler) during maternal incubation and comparison of development with that of other egg‐brooding hylid frogs
inferredcites →https://doi.org/10.1006/bijl.1999.0325openalex-snapshot
Effects of hatching age on development and hatchling morphology in the red-eyed tree frog, Agalychnis callidryas
inferredcites →https://doi.org/10.1007/978-1-4615-3654-3_10openalex-snapshot
The Common Frog Rana temporaria
inferredcites →https://doi.org/10.1007/978-94-009-6536-2_3openalex-snapshot
Transition of respiratory processes during amphibian metamorphosis: from egg to adult
inferredcites →https://doi.org/10.1016/0012-1606(72)90175-3openalex-snapshot
Genetic and experimental studies on a mutant gene (c) determining absence of heart action in embryos of the Mexican axolotl (Ambystoma mexicanum)
inferredcites →https://doi.org/10.1073/pnas.92.8.3507openalex-snapshot
Adaptive plasticity in hatching age: a response to predation risk trade-offs.
inferredcites →https://doi.org/10.1086/physzool.56.4.30155875openalex-snapshot
The Relation of Air Breathing and Locomotion to Predation on Tadpoles, Rana berlandieri, by Turtles
inferredcites →https://doi.org/10.1086/physzool.58.5.30158576openalex-snapshot
Energy Conservation during the Delayed-Hatching Period in the Frog Pseudophryne bibroni
inferredcites →https://doi.org/10.1086/physzool.61.6.30156155openalex-snapshot
Influence of Environmental P o 2 on Embryonic Oxygen Consumption, Rate of Development, and Hatching in the Frog Pseudophryne bibroni
inferredcites →https://doi.org/10.1086/physzool.63.6.30152638openalex-snapshot
Incubation Time and Rate of Embryonic Development in Amphibians: The Influence of Ovum Size, Temperature, and Reproductive Mode
inferredcites →https://doi.org/10.1086/physzool.64.3.30158200openalex-snapshot
Gas Conductance of the Jelly Capsule of Terrestrial Frog Eggs Correlates with Embryonic Stage, Not Metabolic Demand or Ambient P o 2
inferredcites →https://doi.org/10.1086/physzool.68.1.30163915openalex-snapshot
Respiration of Amphibian Eggs
inferredcites →https://doi.org/10.1086/physzool.68.2.30166500openalex-snapshot
Oxygen Uptake by the Aquatic Eggs of the Australian FrogCrinia georgiana
inferredcites →https://doi.org/10.1086/physzool.69.1.30164205openalex-snapshot
Predator-Mediated Selection on Burst Swimming Performance in Tadpoles of the Pacific Tree Frog, Pseudacris regilla
inferredcites →https://doi.org/10.1093/beheco/10.3.251openalex-snapshot
The development of behavioral defenses: a mechanistic analysis of vulnerability in red-eyed tree frog hatchlings
inferredcites →https://doi.org/10.1126/science.159.3810.101openalex-snapshot
Induction and Survival of Hemoglobin-Less and Erythrocyte-Less Tadpoles and Young Bullfrogs
inferredcites →https://doi.org/10.1126/science.7089563openalex-snapshot
Hatching of Amphibian Embryos: The Physiological Trigger
inferredcites →https://doi.org/10.1161/01.res.79.2.358openalex-snapshot
Disruption of Hemoglobin Oxygen Transport Does Not Impact Oxygen-Dependent Physiological Processes in Developing Embryos of Zebra Fish ( Danio rerio )
inferredcites →https://doi.org/10.1201/9781003064565openalex-snapshot
Normal Table of Xenopus Laevis (Daudin)
inferredcites →https://doi.org/10.1242/jeb.108.1.231openalex-snapshot
Aerial Versus Aquatic Oxygen Consumption in Larvae of the Clawed Frog, Xenopus Laevis
inferredcites →https://doi.org/10.1242/jeb.152.1.129openalex-snapshot
Developmental Changes in Cardiac and Metabolic Physiology of the Direct-Developing Tropical FrogEleutherodactylus Coqui
inferredcites →https://doi.org/10.1242/jeb.197.1.31openalex-snapshot
Embryonic and Larval Respiration In the Arboreal foam Nests of the African Frog Chiromantis Xerampelina
inferredcites →https://doi.org/10.1242/jeb.201.9.1461openalex-snapshot
Cardio-Respiratory Ontogeny During Chronic Carbon Monoxide Exposure in the Clawed Frog Xenopus Laevis
inferredcites →https://doi.org/10.2307/1439811openalex-snapshot
Embryonic and Larval Development of Hyla avivoca
inferredcites →https://doi.org/10.2307/1440765openalex-snapshot
Embryonic and Larval Development of Heleioporus eyrei (Amphibia: Leptodactylidae)
inferredcites →https://doi.org/10.2307/1446276openalex-snapshot
The Implications of Shape and Metamorphosis for Drag Forces on a Generalized Pond Tadpole (Rana catesbeiana)
inferredcites →https://doi.org/10.2307/1447109openalex-snapshot
Environmental Physiology of the Amphibians
inferredcites →https://doi.org/10.2307/1564939openalex-snapshot
Observations on the Natural History of Stephopaedes anotis (Bufonidae)
inferredcites →https://doi.org/10.2307/1938739openalex-snapshot
Greater Maternal Investment Can Decrease Offspring Survival in the Frog Bombina Orientalis
inferredcites →https://doi.org/10.2307/2390151openalex-snapshot
Maternal Investment and Developmental Plasticity: Functional Consequences for Locomotor Performance of Hatchling Frog Larvae
inferredcites →https://doi.org/10.2307/3222683openalex-snapshot
Studies on the Normal Development of Scaphiopus bombifrons Cope. II. The Later Embryonic and Larval Periods
inferredcites →https://doi.org/10.2307/3498751openalex-snapshot
Nonparametric Statistics for the Behavioral Sciences
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/vz.76.e205950zenodo-depositor-declared
Cutting out the excess: Reduction of larval structures in Asian tree frogs (Anura: Rhacophoridae) from Vietnam with different modes of reproduction and development
inferred← citeshttps://doi.org/10.1002/jez.1018openalex-snapshot
Do prostaglandins regulate external gill regression in anurans?
inferred← citeshttps://doi.org/10.1002/jmor.10655openalex-snapshot
The external gills of anuran amphibians: Comparative morphology and ultrastructure
inferred← citeshttps://doi.org/10.1007/s00442-007-0708-0openalex-snapshot
To hatch and hatch not: similar selective trade-offs but different responses to egg predators in two closely related, syntopic treefrogs
inferred← citeshttps://doi.org/10.1007/s10228-011-0217-3openalex-snapshot
Embryonic development and larval behavior of the kissing loach (Parabotia curta): adaptations to an ephemeral, hypoxic environment
inferred← citeshttps://doi.org/10.1016/j.anbehav.2005.06.007openalex-snapshot
Development of red-eyed treefrog eggs affects efficiency and choices of egg-foraging wasps
inferred← citeshttps://doi.org/10.1016/j.anbehav.2017.05.008openalex-snapshot
Developmental onset of escape-hatching responses in red-eyed treefrogs depends on cue type
inferred← citeshttps://doi.org/10.1016/j.cbpa.2007.02.009openalex-snapshot
Oxygen, gills, and embryo behavior: mechanisms of adaptive plasticity in hatching
inferred← citeshttps://doi.org/10.1016/j.cbpa.2007.05.027openalex-snapshot
Plasticity in the timing of physiological development: Physiological heterokairy — What is it, how frequent is it, and does it matter?
inferred← citeshttps://doi.org/10.1086/339214openalex-snapshot
Hatching Timing, Oxygen Availability, and External Gill Regression in the Tree Frog,Agalychnis callidryas
inferred← citeshttps://doi.org/10.1086/432849openalex-snapshot
Development, Surface Exposure, and Embryo Behavior Affect Oxygen Levels in Eggs of the Red‐Eyed Treefrog,Agalychnis callidryas
inferred← citeshttps://doi.org/10.1093/biolinnean/blac059openalex-snapshot
Finding a pathway through the rocks: the role of development on the evolution of quasi-terrestriality and the origin of endotrophism in cycloramphids (Anura)
inferred← citeshttps://doi.org/10.1093/biolinnean/bly214openalex-snapshot
Two types of hatching gland cells facilitate escape-hatching at different developmental stages in red-eyed treefrogs,Agalychnis callidryas(Anura: Phyllomedusidae)
inferred← citeshttps://doi.org/10.1093/zoolinnean/zlag081openalex-snapshot
Embryonic development of South American frogs: new insights into the evolution of Neoaustrarana and Telmatobiidae
inferred← citeshttps://doi.org/10.1111/aec.13367openalex-snapshot
The case for studying tadpole autecology, with comments on strategies to study other small, fast‐moving animals in nature
inferred← citeshttps://doi.org/10.1111/jzo.13060openalex-snapshot
Exceptional features of the embryonic ontogeny of a direct‐developing Robber frog
inferred← citeshttps://doi.org/10.11606/issn.2316-9079.v12i1p13-32openalex-snapshot
Estrutura do ninho, incubação e eclosão de Phyllomedusa trinitatis (Anura: Hylidae)
inferred← citeshttps://doi.org/10.1242/jeb.020958openalex-snapshot
External gills and adaptive embryo behavior facilitate synchronous development and hatching plasticity under respiratory constraint
inferred← citeshttps://doi.org/10.1371/journal.pone.0218733openalex-snapshot
Early ontogeny and sequence heterochronies in Leiuperinae frogs (Anura: Leptodactylidae)
inferred← citeshttps://doi.org/10.1655/02-82openalex-snapshot
EVALUATION OF THE HATCHING TRIGGER AND LARVAL ECOLOGY OF THE SALAMANDER AMPHIUMA MEANS
inferred← citeshttps://doi.org/10.1655/07-055.1openalex-snapshot
“EYE OF NEWT AND TOE OF FROG”: HERPETOLOGY IN 21STCENTURY SCIENCE
inferred← citeshttps://doi.org/10.1890/07-0529.1openalex-snapshot
EVOLUTION OF ADAPTIVE PLASTICITY: RISK‐SENSITIVE HATCHING IN NEOTROPICAL LEAF‐BREEDING TREEFROGS
inferred← citeshttps://doi.org/10.1890/12-0194.1openalex-snapshot
Effects of plastic hatching timing carry over through metamorphosis in red‐eyed treefrogs
inferred← citeshttps://doi.org/10.7717/peerj.6018openalex-snapshot
When and where to hatch? Red-eyed treefrog embryos use light cues in two contexts
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