Developmental Plasticity of Scaphiopus Couchii Tadpoles in an Unpredictable Environment
Couch's spadefoot toads (Scaphiopus couchii) breed in ephemeral desert ponds of variable duration. Pond duration depends on initial water depth and frequency of rainfall. In four years on Tornillo Flat (Big Bend National Park, Texas, USA), larvae metamorphosed only from low—density ponds, or po...
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Veröffentlicht in: | Ecology (Durham) 1989-12, Vol.70 (6), p.1775-1787 |
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description | Couch's spadefoot toads (Scaphiopus couchii) breed in ephemeral desert ponds of variable duration. Pond duration depends on initial water depth and frequency of rainfall. In four years on Tornillo Flat (Big Bend National Park, Texas, USA), larvae metamorphosed only from low—density ponds, or ponds that refilled before drying. With sufficient food S. couchii larvae developed very rapidly (8—16 d). Rapid development maximized the probability of completing development before the pond dried, but resulted in small size at metamorphosis. I raised larvae in a factorial field experiment manipulating food level, larval density, and pond duration to test if timing of metamorphosis can be altered by pond drying and to test if the response to drying is affected by growth history. Both pond duration and growth history affected timing of metamorphosis, but pond duration explained most of the variation in timing of metamorphosis. For a given pond duration, larvae in high—food ponds metamorphosed earlier than did larvae in low—food, low—density ponds. Short pond duration accelerated metamorphosis at a smaller size and with relatively smaller hindlimbs. Larvae may actively avoid desiccation by metamorphosing earlier from short—duration ponds, but probably benefit by delaying metamorphosis in longer duration ponds. The similar relations between pond drying and metamorphosis in experimental ponds and natural ponds indicate that developmental plasticity may play an important role in the ecology of this population. |
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Pond duration depends on initial water depth and frequency of rainfall. In four years on Tornillo Flat (Big Bend National Park, Texas, USA), larvae metamorphosed only from low—density ponds, or ponds that refilled before drying. With sufficient food S. couchii larvae developed very rapidly (8—16 d). Rapid development maximized the probability of completing development before the pond dried, but resulted in small size at metamorphosis. I raised larvae in a factorial field experiment manipulating food level, larval density, and pond duration to test if timing of metamorphosis can be altered by pond drying and to test if the response to drying is affected by growth history. Both pond duration and growth history affected timing of metamorphosis, but pond duration explained most of the variation in timing of metamorphosis. For a given pond duration, larvae in high—food ponds metamorphosed earlier than did larvae in low—food, low—density ponds. Short pond duration accelerated metamorphosis at a smaller size and with relatively smaller hindlimbs. Larvae may actively avoid desiccation by metamorphosing earlier from short—duration ponds, but probably benefit by delaying metamorphosis in longer duration ponds. The similar relations between pond drying and metamorphosis in experimental ponds and natural ponds indicate that developmental plasticity may play an important role in the ecology of this population.</description><identifier>ISSN: 0012-9658</identifier><identifier>EISSN: 1939-9170</identifier><identifier>DOI: 10.2307/1938111</identifier><identifier>CODEN: ECGYAQ</identifier><language>eng</language><publisher>Washington, DC: Ecological Society of America</publisher><subject>amphibian ; Amphibians ; Animal and plant ecology ; Animal, plant and microbial ecology ; Animals ; Autoecology ; Biological and medical sciences ; density ; desert ; Deserts ; Drying ; Ecology ; food level ; Freshwater ecology ; Fundamental and applied biological sciences. Psychology ; growth ; Larvae ; Larval development ; Metamorphosis ; phenotypic plasticity ; Ponds ; Reptiles & amphibians ; Reptilia. Amphibia ; Scaphiopus couchii ; spadefoot toad ; tadpole ; Tadpoles ; temporary pond ; Trajectories ; Vertebrata</subject><ispartof>Ecology (Durham), 1989-12, Vol.70 (6), p.1775-1787</ispartof><rights>Copyright 1989 The Ecological Society of America</rights><rights>1989 by the Ecological Society of America</rights><rights>1990 INIST-CNRS</rights><rights>Copyright Ecological Society of America Dec 1989</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4045-394e2563b6fb66eb43aeb9eb17ebb4a05abff0da6e9628eecd8d68679214f4633</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/1938111$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/1938111$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,799,27846,27901,27902,57992,58225</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6701338$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Newman, Robert A.</creatorcontrib><title>Developmental Plasticity of Scaphiopus Couchii Tadpoles in an Unpredictable Environment</title><title>Ecology (Durham)</title><description>Couch's spadefoot toads (Scaphiopus couchii) breed in ephemeral desert ponds of variable duration. Pond duration depends on initial water depth and frequency of rainfall. In four years on Tornillo Flat (Big Bend National Park, Texas, USA), larvae metamorphosed only from low—density ponds, or ponds that refilled before drying. With sufficient food S. couchii larvae developed very rapidly (8—16 d). Rapid development maximized the probability of completing development before the pond dried, but resulted in small size at metamorphosis. I raised larvae in a factorial field experiment manipulating food level, larval density, and pond duration to test if timing of metamorphosis can be altered by pond drying and to test if the response to drying is affected by growth history. Both pond duration and growth history affected timing of metamorphosis, but pond duration explained most of the variation in timing of metamorphosis. For a given pond duration, larvae in high—food ponds metamorphosed earlier than did larvae in low—food, low—density ponds. Short pond duration accelerated metamorphosis at a smaller size and with relatively smaller hindlimbs. Larvae may actively avoid desiccation by metamorphosing earlier from short—duration ponds, but probably benefit by delaying metamorphosis in longer duration ponds. The similar relations between pond drying and metamorphosis in experimental ponds and natural ponds indicate that developmental plasticity may play an important role in the ecology of this population.</description><subject>amphibian</subject><subject>Amphibians</subject><subject>Animal and plant ecology</subject><subject>Animal, plant and microbial ecology</subject><subject>Animals</subject><subject>Autoecology</subject><subject>Biological and medical sciences</subject><subject>density</subject><subject>desert</subject><subject>Deserts</subject><subject>Drying</subject><subject>Ecology</subject><subject>food level</subject><subject>Freshwater ecology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>growth</subject><subject>Larvae</subject><subject>Larval development</subject><subject>Metamorphosis</subject><subject>phenotypic plasticity</subject><subject>Ponds</subject><subject>Reptiles & amphibians</subject><subject>Reptilia. Amphibia</subject><subject>Scaphiopus couchii</subject><subject>spadefoot toad</subject><subject>tadpole</subject><subject>Tadpoles</subject><subject>temporary pond</subject><subject>Trajectories</subject><subject>Vertebrata</subject><issn>0012-9658</issn><issn>1939-9170</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>K30</sourceid><recordid>eNp90F1rFDEUBuBBFFyr-BMMKvRqNCfJ5ONS1q0KBYV2Ea-GJHNis0wnYzJb2X9vyi56VXNzcvHwno-meQn0HeNUvQfDNQA8alb1Z1oDij5uVpQCa43s9NPmWSk7Wh8IvWq-f8Q7HNN8i9NiR_JttGWJPi4HkgK58na-iWneF7JOe38TI7m2w5xGLCROxE5kO80Zh-gX60Ykm-ku5jTdZz1vngQ7FnxxqmfN9mJzvf7cXn799GX94bL1goqu5UYg6yR3Mjgp0Qlu0Rl0oNA5YWlnXQh0sBKNZBrRD3qQWirDQAQhOT9rXh9z55x-7bEs_S7t81Rb9gy0qU7Sit48hIAZKbjWSlV1flQ-p1Iyhn7O8dbmQw-0vz9tfzptlW9PebZ4O4ZsJx_LXy4VBc51ZfzIfscRDw-l9Zv1DzDaKCpBqe5f-K4sKf9nhldHFmzq7c9c-2-vGK3rUlBMguB_AGVUmmc</recordid><startdate>198912</startdate><enddate>198912</enddate><creator>Newman, Robert A.</creator><general>Ecological Society of America</general><general>The Ecological Society of America</general><general>Brooklyn Botanic Garden, etc</general><scope>FBQ</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>FIXVA</scope><scope>FKUCP</scope><scope>IOIBA</scope><scope>K30</scope><scope>PAAUG</scope><scope>PAWHS</scope><scope>PAWZZ</scope><scope>PAXOH</scope><scope>PBHAV</scope><scope>PBQSW</scope><scope>PBYQZ</scope><scope>PCIWU</scope><scope>PCMID</scope><scope>PCZJX</scope><scope>PDGRG</scope><scope>PDWWI</scope><scope>PETMR</scope><scope>PFVGT</scope><scope>PGXDX</scope><scope>PIHIL</scope><scope>PISVA</scope><scope>PJCTQ</scope><scope>PJTMS</scope><scope>PLCHJ</scope><scope>PMHAD</scope><scope>PNQDJ</scope><scope>POUND</scope><scope>PPLAD</scope><scope>PQAPC</scope><scope>PQCAN</scope><scope>PQCMW</scope><scope>PQEME</scope><scope>PQHKH</scope><scope>PQMID</scope><scope>PQNCT</scope><scope>PQNET</scope><scope>PQSCT</scope><scope>PQSET</scope><scope>PSVJG</scope><scope>PVMQY</scope><scope>PZGFC</scope><scope>7QG</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>SOI</scope></search><sort><creationdate>198912</creationdate><title>Developmental Plasticity of Scaphiopus Couchii Tadpoles in an Unpredictable Environment</title><author>Newman, Robert A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4045-394e2563b6fb66eb43aeb9eb17ebb4a05abff0da6e9628eecd8d68679214f4633</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>amphibian</topic><topic>Amphibians</topic><topic>Animal and plant ecology</topic><topic>Animal, plant and microbial ecology</topic><topic>Animals</topic><topic>Autoecology</topic><topic>Biological and medical sciences</topic><topic>density</topic><topic>desert</topic><topic>Deserts</topic><topic>Drying</topic><topic>Ecology</topic><topic>food level</topic><topic>Freshwater ecology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>growth</topic><topic>Larvae</topic><topic>Larval development</topic><topic>Metamorphosis</topic><topic>phenotypic plasticity</topic><topic>Ponds</topic><topic>Reptiles & amphibians</topic><topic>Reptilia. Amphibia</topic><topic>Scaphiopus couchii</topic><topic>spadefoot toad</topic><topic>tadpole</topic><topic>Tadpoles</topic><topic>temporary pond</topic><topic>Trajectories</topic><topic>Vertebrata</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Newman, Robert A.</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Periodicals Index Online Segment 03</collection><collection>Periodicals Index Online Segment 04</collection><collection>Periodicals Index Online Segment 29</collection><collection>Periodicals Index Online</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - West</collection><collection>Primary Sources Access (Plan D) - International</collection><collection>Primary Sources Access & Build (Plan A) - MEA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Midwest</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Northeast</collection><collection>Primary Sources Access (Plan D) - Southeast</collection><collection>Primary Sources Access (Plan D) - North Central</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Southeast</collection><collection>Primary Sources Access (Plan D) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - UK / I</collection><collection>Primary Sources Access (Plan D) - Canada</collection><collection>Primary Sources Access (Plan D) - EMEALA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - North Central</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - International</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - International</collection><collection>Primary Sources Access (Plan D) - West</collection><collection>Periodicals Index Online Segments 1-50</collection><collection>Primary Sources Access (Plan D) - APAC</collection><collection>Primary Sources Access (Plan D) - Midwest</collection><collection>Primary Sources Access (Plan D) - MEA</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - Canada</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - UK / I</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - EMEALA</collection><collection>Primary Sources Access & Build (Plan A) - APAC</collection><collection>Primary Sources Access & Build (Plan A) - Canada</collection><collection>Primary Sources Access & Build (Plan A) - West</collection><collection>Primary Sources Access & Build (Plan A) - EMEALA</collection><collection>Primary Sources Access (Plan D) - Northeast</collection><collection>Primary Sources Access & Build (Plan A) - Midwest</collection><collection>Primary Sources Access & Build (Plan A) - North Central</collection><collection>Primary Sources Access & Build (Plan A) - Northeast</collection><collection>Primary Sources Access & Build (Plan A) - South Central</collection><collection>Primary Sources Access & Build (Plan A) - Southeast</collection><collection>Primary Sources Access (Plan D) - UK / I</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - APAC</collection><collection>Primary Sources Access—Foundation Edition (Plan E) - MEA</collection><collection>Animal Behavior Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>Environment Abstracts</collection><jtitle>Ecology (Durham)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Newman, Robert A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Developmental Plasticity of Scaphiopus Couchii Tadpoles in an Unpredictable Environment</atitle><jtitle>Ecology (Durham)</jtitle><date>1989-12</date><risdate>1989</risdate><volume>70</volume><issue>6</issue><spage>1775</spage><epage>1787</epage><pages>1775-1787</pages><issn>0012-9658</issn><eissn>1939-9170</eissn><coden>ECGYAQ</coden><abstract>Couch's spadefoot toads (Scaphiopus couchii) breed in ephemeral desert ponds of variable duration. Pond duration depends on initial water depth and frequency of rainfall. In four years on Tornillo Flat (Big Bend National Park, Texas, USA), larvae metamorphosed only from low—density ponds, or ponds that refilled before drying. With sufficient food S. couchii larvae developed very rapidly (8—16 d). Rapid development maximized the probability of completing development before the pond dried, but resulted in small size at metamorphosis. I raised larvae in a factorial field experiment manipulating food level, larval density, and pond duration to test if timing of metamorphosis can be altered by pond drying and to test if the response to drying is affected by growth history. Both pond duration and growth history affected timing of metamorphosis, but pond duration explained most of the variation in timing of metamorphosis. For a given pond duration, larvae in high—food ponds metamorphosed earlier than did larvae in low—food, low—density ponds. Short pond duration accelerated metamorphosis at a smaller size and with relatively smaller hindlimbs. Larvae may actively avoid desiccation by metamorphosing earlier from short—duration ponds, but probably benefit by delaying metamorphosis in longer duration ponds. The similar relations between pond drying and metamorphosis in experimental ponds and natural ponds indicate that developmental plasticity may play an important role in the ecology of this population.</abstract><cop>Washington, DC</cop><pub>Ecological Society of America</pub><doi>10.2307/1938111</doi><tpages>13</tpages></addata></record> |
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source | Jstor Complete Legacy; Periodicals Index Online |
subjects | amphibian Amphibians Animal and plant ecology Animal, plant and microbial ecology Animals Autoecology Biological and medical sciences density desert Deserts Drying Ecology food level Freshwater ecology Fundamental and applied biological sciences. Psychology growth Larvae Larval development Metamorphosis phenotypic plasticity Ponds Reptiles & amphibians Reptilia. Amphibia Scaphiopus couchii spadefoot toad tadpole Tadpoles temporary pond Trajectories Vertebrata |
title | Developmental Plasticity of Scaphiopus Couchii Tadpoles in an Unpredictable Environment |
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