In situ shifts of predominance between autotrophic and heterotrophic feeding in the reef-building coral Mussismilia hispida: an approach using fatty acid trophic markers
Abstract Many species of reef-building corals are mixotrophic, relying on both photoautotrophy performed by their dinoflagellate symbionts and heterotrophy from consumption of zooplankton. Autotrophy and heterotrophy supply corals with specific ω3 fatty acids, which can be used as trophic markers an...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Mies, M. [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2018 |
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| Schlagwörter: |
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| Anmerkung: |
© Springer-Verlag GmbH Germany, part of Springer Nature 2018 |
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| Übergeordnetes Werk: |
Enthalten in: Coral reefs - Berlin : Springer, 1982, 37(2018), 3 vom: 07. Mai, Seite 677-689 |
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| Übergeordnetes Werk: |
volume:37 ; year:2018 ; number:3 ; day:07 ; month:05 ; pages:677-689 |
| Links: |
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| DOI / URN: |
10.1007/s00338-018-1692-z |
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| Katalog-ID: |
SPR004063104 |
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| 520 | |a Abstract Many species of reef-building corals are mixotrophic, relying on both photoautotrophy performed by their dinoflagellate symbionts and heterotrophy from consumption of zooplankton. Autotrophy and heterotrophy supply corals with specific ω3 fatty acids, which can be used as trophic markers and record the contribution of each feeding strategy. This study investigated whether the reef-building coral Mussismilia hispida, endemic to Brazil, is able to shift between predominantly autotrophic and predominantly heterotrophic by monitoring the concentration of fatty acids in the host tissue. We then examined whether shifts are related to changes in temperature and wind stress. For that purpose, M. hispida colonies were monitored for a year with monthly tissue sampling. Symbiont concentration was determined and lipid extraction performed. Four fatty acids were quantitatively analyzed by gas chromatography with flame ionization detector: the autotrophy markers: stearidonic acid (SDA), docosapentaenoic acid (DPA), docosahexaenoic acid (DHA), and a heterotrophy marker: cis-gondoic acid (CGA). Three preliminary experiments confirmed the specificity of SDA, DPA and CGA, but not of DHA. Shifts of predominance occurred multiple times during the year and were associated with minimal temperatures and wind stress. Colonies underwent mild bleaching during summer months, which they seemed to compensate with heterotrophic feeding. Our major findings include the validation of three FATM and a trophic index for coral reef ecology studies and also describing the in situ occurrences of shifts between feeding modes, while highlighting the role of temperature and meteorological events. | ||
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| 650 | 4 | |a Scleractinia |7 (dpeaa)DE-He213 | |
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| 700 | 1 | |a Tenório, A. A. |4 aut | |
| 700 | 1 | |a Banha, T. N. S. |4 aut | |
| 700 | 1 | |a Waters, L. G. |4 aut | |
| 700 | 1 | |a Polito, P. S. |4 aut | |
| 700 | 1 | |a Taniguchi, S. |4 aut | |
| 700 | 1 | |a Bícego, M. C. |4 aut | |
| 700 | 1 | |a Sumida, P. Y. G. |4 aut | |
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10.1007/s00338-018-1692-z doi (DE-627)SPR004063104 (SPR)s00338-018-1692-z-e DE-627 ger DE-627 rakwb eng Mies, M. verfasserin (orcid)0000-0001-8925-7037 aut In situ shifts of predominance between autotrophic and heterotrophic feeding in the reef-building coral Mussismilia hispida: an approach using fatty acid trophic markers 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag GmbH Germany, part of Springer Nature 2018 Abstract Many species of reef-building corals are mixotrophic, relying on both photoautotrophy performed by their dinoflagellate symbionts and heterotrophy from consumption of zooplankton. Autotrophy and heterotrophy supply corals with specific ω3 fatty acids, which can be used as trophic markers and record the contribution of each feeding strategy. This study investigated whether the reef-building coral Mussismilia hispida, endemic to Brazil, is able to shift between predominantly autotrophic and predominantly heterotrophic by monitoring the concentration of fatty acids in the host tissue. We then examined whether shifts are related to changes in temperature and wind stress. For that purpose, M. hispida colonies were monitored for a year with monthly tissue sampling. Symbiont concentration was determined and lipid extraction performed. Four fatty acids were quantitatively analyzed by gas chromatography with flame ionization detector: the autotrophy markers: stearidonic acid (SDA), docosapentaenoic acid (DPA), docosahexaenoic acid (DHA), and a heterotrophy marker: cis-gondoic acid (CGA). Three preliminary experiments confirmed the specificity of SDA, DPA and CGA, but not of DHA. Shifts of predominance occurred multiple times during the year and were associated with minimal temperatures and wind stress. Colonies underwent mild bleaching during summer months, which they seemed to compensate with heterotrophic feeding. Our major findings include the validation of three FATM and a trophic index for coral reef ecology studies and also describing the in situ occurrences of shifts between feeding modes, while highlighting the role of temperature and meteorological events. Mixotrophy (dpeaa)DE-He213 Lipids (dpeaa)DE-He213 Bleaching (dpeaa)DE-He213 Scleractinia (dpeaa)DE-He213 Chromatography (dpeaa)DE-He213 Güth, A. Z. aut Tenório, A. A. aut Banha, T. N. S. aut Waters, L. G. aut Polito, P. S. aut Taniguchi, S. aut Bícego, M. C. aut Sumida, P. Y. G. aut Enthalten in Coral reefs Berlin : Springer, 1982 37(2018), 3 vom: 07. Mai, Seite 677-689 (DE-627)268756112 (DE-600)1472576-9 1432-0975 nnns volume:37 year:2018 number:3 day:07 month:05 pages:677-689 https://dx.doi.org/10.1007/s00338-018-1692-z lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 37 2018 3 07 05 677-689 |
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10.1007/s00338-018-1692-z doi (DE-627)SPR004063104 (SPR)s00338-018-1692-z-e DE-627 ger DE-627 rakwb eng Mies, M. verfasserin (orcid)0000-0001-8925-7037 aut In situ shifts of predominance between autotrophic and heterotrophic feeding in the reef-building coral Mussismilia hispida: an approach using fatty acid trophic markers 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag GmbH Germany, part of Springer Nature 2018 Abstract Many species of reef-building corals are mixotrophic, relying on both photoautotrophy performed by their dinoflagellate symbionts and heterotrophy from consumption of zooplankton. Autotrophy and heterotrophy supply corals with specific ω3 fatty acids, which can be used as trophic markers and record the contribution of each feeding strategy. This study investigated whether the reef-building coral Mussismilia hispida, endemic to Brazil, is able to shift between predominantly autotrophic and predominantly heterotrophic by monitoring the concentration of fatty acids in the host tissue. We then examined whether shifts are related to changes in temperature and wind stress. For that purpose, M. hispida colonies were monitored for a year with monthly tissue sampling. Symbiont concentration was determined and lipid extraction performed. Four fatty acids were quantitatively analyzed by gas chromatography with flame ionization detector: the autotrophy markers: stearidonic acid (SDA), docosapentaenoic acid (DPA), docosahexaenoic acid (DHA), and a heterotrophy marker: cis-gondoic acid (CGA). Three preliminary experiments confirmed the specificity of SDA, DPA and CGA, but not of DHA. Shifts of predominance occurred multiple times during the year and were associated with minimal temperatures and wind stress. Colonies underwent mild bleaching during summer months, which they seemed to compensate with heterotrophic feeding. Our major findings include the validation of three FATM and a trophic index for coral reef ecology studies and also describing the in situ occurrences of shifts between feeding modes, while highlighting the role of temperature and meteorological events. Mixotrophy (dpeaa)DE-He213 Lipids (dpeaa)DE-He213 Bleaching (dpeaa)DE-He213 Scleractinia (dpeaa)DE-He213 Chromatography (dpeaa)DE-He213 Güth, A. Z. aut Tenório, A. A. aut Banha, T. N. S. aut Waters, L. G. aut Polito, P. S. aut Taniguchi, S. aut Bícego, M. C. aut Sumida, P. Y. G. aut Enthalten in Coral reefs Berlin : Springer, 1982 37(2018), 3 vom: 07. Mai, Seite 677-689 (DE-627)268756112 (DE-600)1472576-9 1432-0975 nnns volume:37 year:2018 number:3 day:07 month:05 pages:677-689 https://dx.doi.org/10.1007/s00338-018-1692-z lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 37 2018 3 07 05 677-689 |
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10.1007/s00338-018-1692-z doi (DE-627)SPR004063104 (SPR)s00338-018-1692-z-e DE-627 ger DE-627 rakwb eng Mies, M. verfasserin (orcid)0000-0001-8925-7037 aut In situ shifts of predominance between autotrophic and heterotrophic feeding in the reef-building coral Mussismilia hispida: an approach using fatty acid trophic markers 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag GmbH Germany, part of Springer Nature 2018 Abstract Many species of reef-building corals are mixotrophic, relying on both photoautotrophy performed by their dinoflagellate symbionts and heterotrophy from consumption of zooplankton. Autotrophy and heterotrophy supply corals with specific ω3 fatty acids, which can be used as trophic markers and record the contribution of each feeding strategy. This study investigated whether the reef-building coral Mussismilia hispida, endemic to Brazil, is able to shift between predominantly autotrophic and predominantly heterotrophic by monitoring the concentration of fatty acids in the host tissue. We then examined whether shifts are related to changes in temperature and wind stress. For that purpose, M. hispida colonies were monitored for a year with monthly tissue sampling. Symbiont concentration was determined and lipid extraction performed. Four fatty acids were quantitatively analyzed by gas chromatography with flame ionization detector: the autotrophy markers: stearidonic acid (SDA), docosapentaenoic acid (DPA), docosahexaenoic acid (DHA), and a heterotrophy marker: cis-gondoic acid (CGA). Three preliminary experiments confirmed the specificity of SDA, DPA and CGA, but not of DHA. Shifts of predominance occurred multiple times during the year and were associated with minimal temperatures and wind stress. Colonies underwent mild bleaching during summer months, which they seemed to compensate with heterotrophic feeding. Our major findings include the validation of three FATM and a trophic index for coral reef ecology studies and also describing the in situ occurrences of shifts between feeding modes, while highlighting the role of temperature and meteorological events. Mixotrophy (dpeaa)DE-He213 Lipids (dpeaa)DE-He213 Bleaching (dpeaa)DE-He213 Scleractinia (dpeaa)DE-He213 Chromatography (dpeaa)DE-He213 Güth, A. Z. aut Tenório, A. A. aut Banha, T. N. S. aut Waters, L. G. aut Polito, P. S. aut Taniguchi, S. aut Bícego, M. C. aut Sumida, P. Y. G. aut Enthalten in Coral reefs Berlin : Springer, 1982 37(2018), 3 vom: 07. Mai, Seite 677-689 (DE-627)268756112 (DE-600)1472576-9 1432-0975 nnns volume:37 year:2018 number:3 day:07 month:05 pages:677-689 https://dx.doi.org/10.1007/s00338-018-1692-z lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 37 2018 3 07 05 677-689 |
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10.1007/s00338-018-1692-z doi (DE-627)SPR004063104 (SPR)s00338-018-1692-z-e DE-627 ger DE-627 rakwb eng Mies, M. verfasserin (orcid)0000-0001-8925-7037 aut In situ shifts of predominance between autotrophic and heterotrophic feeding in the reef-building coral Mussismilia hispida: an approach using fatty acid trophic markers 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag GmbH Germany, part of Springer Nature 2018 Abstract Many species of reef-building corals are mixotrophic, relying on both photoautotrophy performed by their dinoflagellate symbionts and heterotrophy from consumption of zooplankton. Autotrophy and heterotrophy supply corals with specific ω3 fatty acids, which can be used as trophic markers and record the contribution of each feeding strategy. This study investigated whether the reef-building coral Mussismilia hispida, endemic to Brazil, is able to shift between predominantly autotrophic and predominantly heterotrophic by monitoring the concentration of fatty acids in the host tissue. We then examined whether shifts are related to changes in temperature and wind stress. For that purpose, M. hispida colonies were monitored for a year with monthly tissue sampling. Symbiont concentration was determined and lipid extraction performed. Four fatty acids were quantitatively analyzed by gas chromatography with flame ionization detector: the autotrophy markers: stearidonic acid (SDA), docosapentaenoic acid (DPA), docosahexaenoic acid (DHA), and a heterotrophy marker: cis-gondoic acid (CGA). Three preliminary experiments confirmed the specificity of SDA, DPA and CGA, but not of DHA. Shifts of predominance occurred multiple times during the year and were associated with minimal temperatures and wind stress. Colonies underwent mild bleaching during summer months, which they seemed to compensate with heterotrophic feeding. Our major findings include the validation of three FATM and a trophic index for coral reef ecology studies and also describing the in situ occurrences of shifts between feeding modes, while highlighting the role of temperature and meteorological events. Mixotrophy (dpeaa)DE-He213 Lipids (dpeaa)DE-He213 Bleaching (dpeaa)DE-He213 Scleractinia (dpeaa)DE-He213 Chromatography (dpeaa)DE-He213 Güth, A. Z. aut Tenório, A. A. aut Banha, T. N. S. aut Waters, L. G. aut Polito, P. S. aut Taniguchi, S. aut Bícego, M. C. aut Sumida, P. Y. G. aut Enthalten in Coral reefs Berlin : Springer, 1982 37(2018), 3 vom: 07. Mai, Seite 677-689 (DE-627)268756112 (DE-600)1472576-9 1432-0975 nnns volume:37 year:2018 number:3 day:07 month:05 pages:677-689 https://dx.doi.org/10.1007/s00338-018-1692-z lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 37 2018 3 07 05 677-689 |
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10.1007/s00338-018-1692-z doi (DE-627)SPR004063104 (SPR)s00338-018-1692-z-e DE-627 ger DE-627 rakwb eng Mies, M. verfasserin (orcid)0000-0001-8925-7037 aut In situ shifts of predominance between autotrophic and heterotrophic feeding in the reef-building coral Mussismilia hispida: an approach using fatty acid trophic markers 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag GmbH Germany, part of Springer Nature 2018 Abstract Many species of reef-building corals are mixotrophic, relying on both photoautotrophy performed by their dinoflagellate symbionts and heterotrophy from consumption of zooplankton. Autotrophy and heterotrophy supply corals with specific ω3 fatty acids, which can be used as trophic markers and record the contribution of each feeding strategy. This study investigated whether the reef-building coral Mussismilia hispida, endemic to Brazil, is able to shift between predominantly autotrophic and predominantly heterotrophic by monitoring the concentration of fatty acids in the host tissue. We then examined whether shifts are related to changes in temperature and wind stress. For that purpose, M. hispida colonies were monitored for a year with monthly tissue sampling. Symbiont concentration was determined and lipid extraction performed. Four fatty acids were quantitatively analyzed by gas chromatography with flame ionization detector: the autotrophy markers: stearidonic acid (SDA), docosapentaenoic acid (DPA), docosahexaenoic acid (DHA), and a heterotrophy marker: cis-gondoic acid (CGA). Three preliminary experiments confirmed the specificity of SDA, DPA and CGA, but not of DHA. Shifts of predominance occurred multiple times during the year and were associated with minimal temperatures and wind stress. Colonies underwent mild bleaching during summer months, which they seemed to compensate with heterotrophic feeding. Our major findings include the validation of three FATM and a trophic index for coral reef ecology studies and also describing the in situ occurrences of shifts between feeding modes, while highlighting the role of temperature and meteorological events. Mixotrophy (dpeaa)DE-He213 Lipids (dpeaa)DE-He213 Bleaching (dpeaa)DE-He213 Scleractinia (dpeaa)DE-He213 Chromatography (dpeaa)DE-He213 Güth, A. Z. aut Tenório, A. A. aut Banha, T. N. S. aut Waters, L. G. aut Polito, P. S. aut Taniguchi, S. aut Bícego, M. C. aut Sumida, P. Y. G. aut Enthalten in Coral reefs Berlin : Springer, 1982 37(2018), 3 vom: 07. Mai, Seite 677-689 (DE-627)268756112 (DE-600)1472576-9 1432-0975 nnns volume:37 year:2018 number:3 day:07 month:05 pages:677-689 https://dx.doi.org/10.1007/s00338-018-1692-z lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 37 2018 3 07 05 677-689 |
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Enthalten in Coral reefs 37(2018), 3 vom: 07. Mai, Seite 677-689 volume:37 year:2018 number:3 day:07 month:05 pages:677-689 |
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Enthalten in Coral reefs 37(2018), 3 vom: 07. Mai, Seite 677-689 volume:37 year:2018 number:3 day:07 month:05 pages:677-689 |
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Mies, M. @@aut@@ Güth, A. Z. @@aut@@ Tenório, A. A. @@aut@@ Banha, T. N. S. @@aut@@ Waters, L. G. @@aut@@ Polito, P. S. @@aut@@ Taniguchi, S. @@aut@@ Bícego, M. C. @@aut@@ Sumida, P. Y. G. @@aut@@ |
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Autotrophy and heterotrophy supply corals with specific ω3 fatty acids, which can be used as trophic markers and record the contribution of each feeding strategy. This study investigated whether the reef-building coral Mussismilia hispida, endemic to Brazil, is able to shift between predominantly autotrophic and predominantly heterotrophic by monitoring the concentration of fatty acids in the host tissue. We then examined whether shifts are related to changes in temperature and wind stress. For that purpose, M. hispida colonies were monitored for a year with monthly tissue sampling. Symbiont concentration was determined and lipid extraction performed. Four fatty acids were quantitatively analyzed by gas chromatography with flame ionization detector: the autotrophy markers: stearidonic acid (SDA), docosapentaenoic acid (DPA), docosahexaenoic acid (DHA), and a heterotrophy marker: cis-gondoic acid (CGA). Three preliminary experiments confirmed the specificity of SDA, DPA and CGA, but not of DHA. Shifts of predominance occurred multiple times during the year and were associated with minimal temperatures and wind stress. Colonies underwent mild bleaching during summer months, which they seemed to compensate with heterotrophic feeding. 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Mies, M. |
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Mies, M. misc Mixotrophy misc Lipids misc Bleaching misc Scleractinia misc Chromatography In situ shifts of predominance between autotrophic and heterotrophic feeding in the reef-building coral Mussismilia hispida: an approach using fatty acid trophic markers |
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In situ shifts of predominance between autotrophic and heterotrophic feeding in the reef-building coral Mussismilia hispida: an approach using fatty acid trophic markers Mixotrophy (dpeaa)DE-He213 Lipids (dpeaa)DE-He213 Bleaching (dpeaa)DE-He213 Scleractinia (dpeaa)DE-He213 Chromatography (dpeaa)DE-He213 |
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In situ shifts of predominance between autotrophic and heterotrophic feeding in the reef-building coral Mussismilia hispida: an approach using fatty acid trophic markers |
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In situ shifts of predominance between autotrophic and heterotrophic feeding in the reef-building coral Mussismilia hispida: an approach using fatty acid trophic markers |
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Mies, M. Güth, A. Z. Tenório, A. A. Banha, T. N. S. Waters, L. G. Polito, P. S. Taniguchi, S. Bícego, M. C. Sumida, P. Y. G. |
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in situ shifts of predominance between autotrophic and heterotrophic feeding in the reef-building coral mussismilia hispida: an approach using fatty acid trophic markers |
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In situ shifts of predominance between autotrophic and heterotrophic feeding in the reef-building coral Mussismilia hispida: an approach using fatty acid trophic markers |
| abstract |
Abstract Many species of reef-building corals are mixotrophic, relying on both photoautotrophy performed by their dinoflagellate symbionts and heterotrophy from consumption of zooplankton. Autotrophy and heterotrophy supply corals with specific ω3 fatty acids, which can be used as trophic markers and record the contribution of each feeding strategy. This study investigated whether the reef-building coral Mussismilia hispida, endemic to Brazil, is able to shift between predominantly autotrophic and predominantly heterotrophic by monitoring the concentration of fatty acids in the host tissue. We then examined whether shifts are related to changes in temperature and wind stress. For that purpose, M. hispida colonies were monitored for a year with monthly tissue sampling. Symbiont concentration was determined and lipid extraction performed. Four fatty acids were quantitatively analyzed by gas chromatography with flame ionization detector: the autotrophy markers: stearidonic acid (SDA), docosapentaenoic acid (DPA), docosahexaenoic acid (DHA), and a heterotrophy marker: cis-gondoic acid (CGA). Three preliminary experiments confirmed the specificity of SDA, DPA and CGA, but not of DHA. Shifts of predominance occurred multiple times during the year and were associated with minimal temperatures and wind stress. Colonies underwent mild bleaching during summer months, which they seemed to compensate with heterotrophic feeding. Our major findings include the validation of three FATM and a trophic index for coral reef ecology studies and also describing the in situ occurrences of shifts between feeding modes, while highlighting the role of temperature and meteorological events. © Springer-Verlag GmbH Germany, part of Springer Nature 2018 |
| abstractGer |
Abstract Many species of reef-building corals are mixotrophic, relying on both photoautotrophy performed by their dinoflagellate symbionts and heterotrophy from consumption of zooplankton. Autotrophy and heterotrophy supply corals with specific ω3 fatty acids, which can be used as trophic markers and record the contribution of each feeding strategy. This study investigated whether the reef-building coral Mussismilia hispida, endemic to Brazil, is able to shift between predominantly autotrophic and predominantly heterotrophic by monitoring the concentration of fatty acids in the host tissue. We then examined whether shifts are related to changes in temperature and wind stress. For that purpose, M. hispida colonies were monitored for a year with monthly tissue sampling. Symbiont concentration was determined and lipid extraction performed. Four fatty acids were quantitatively analyzed by gas chromatography with flame ionization detector: the autotrophy markers: stearidonic acid (SDA), docosapentaenoic acid (DPA), docosahexaenoic acid (DHA), and a heterotrophy marker: cis-gondoic acid (CGA). Three preliminary experiments confirmed the specificity of SDA, DPA and CGA, but not of DHA. Shifts of predominance occurred multiple times during the year and were associated with minimal temperatures and wind stress. Colonies underwent mild bleaching during summer months, which they seemed to compensate with heterotrophic feeding. Our major findings include the validation of three FATM and a trophic index for coral reef ecology studies and also describing the in situ occurrences of shifts between feeding modes, while highlighting the role of temperature and meteorological events. © Springer-Verlag GmbH Germany, part of Springer Nature 2018 |
| abstract_unstemmed |
Abstract Many species of reef-building corals are mixotrophic, relying on both photoautotrophy performed by their dinoflagellate symbionts and heterotrophy from consumption of zooplankton. Autotrophy and heterotrophy supply corals with specific ω3 fatty acids, which can be used as trophic markers and record the contribution of each feeding strategy. This study investigated whether the reef-building coral Mussismilia hispida, endemic to Brazil, is able to shift between predominantly autotrophic and predominantly heterotrophic by monitoring the concentration of fatty acids in the host tissue. We then examined whether shifts are related to changes in temperature and wind stress. For that purpose, M. hispida colonies were monitored for a year with monthly tissue sampling. Symbiont concentration was determined and lipid extraction performed. Four fatty acids were quantitatively analyzed by gas chromatography with flame ionization detector: the autotrophy markers: stearidonic acid (SDA), docosapentaenoic acid (DPA), docosahexaenoic acid (DHA), and a heterotrophy marker: cis-gondoic acid (CGA). Three preliminary experiments confirmed the specificity of SDA, DPA and CGA, but not of DHA. Shifts of predominance occurred multiple times during the year and were associated with minimal temperatures and wind stress. Colonies underwent mild bleaching during summer months, which they seemed to compensate with heterotrophic feeding. Our major findings include the validation of three FATM and a trophic index for coral reef ecology studies and also describing the in situ occurrences of shifts between feeding modes, while highlighting the role of temperature and meteorological events. © Springer-Verlag GmbH Germany, part of Springer Nature 2018 |
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| title_short |
In situ shifts of predominance between autotrophic and heterotrophic feeding in the reef-building coral Mussismilia hispida: an approach using fatty acid trophic markers |
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https://dx.doi.org/10.1007/s00338-018-1692-z |
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Güth, A. Z. Tenório, A. A. Banha, T. N. S. Waters, L. G. Polito, P. S. Taniguchi, S. Bícego, M. C. Sumida, P. Y. G. |
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Güth, A. Z. Tenório, A. A. Banha, T. N. S. Waters, L. G. Polito, P. S. Taniguchi, S. Bícego, M. C. Sumida, P. Y. G. |
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| score |
7.4008837 |