Bioerosion of coral reefs by two Hawaiian parrotfishes: species, size differences and fishery implications

Abstract Parrotfishes can be significant bioeroders and sediment producers on coral reefs. We quantified the bioerosion rates of two similarly sized Hawaiian parrotfishes with two different feeding modes (Scarus rubroviolaceus—a scraper and Chlorurus perspicillatus—an excavator). The results showed...
Ausführliche Beschreibung

Gespeichert in:

Autor*in:	Ong, Ling [verfasserIn] Holland, Kim N.

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2010

Schlagwörter:	Fork Length Fore Reef Bite Volume Live Coral Turf Alga

Anmerkung:	© Springer-Verlag 2010

Übergeordnetes Werk:	Enthalten in: Marine biology - Berlin : Springer, 1967, 157(2010), 6 vom: 05. März, Seite 1313-1323
Übergeordnetes Werk:	volume:157 ; year:2010 ; number:6 ; day:05 ; month:03 ; pages:1313-1323

Links:	Volltext

DOI / URN:	10.1007/s00227-010-1411-y

Katalog-ID:	SPR002538431

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520			\|a Abstract Parrotfishes can be significant bioeroders and sediment producers on coral reefs. We quantified the bioerosion rates of two similarly sized Hawaiian parrotfishes with two different feeding modes (Scarus rubroviolaceus—a scraper and Chlorurus perspicillatus—an excavator). The results showed that feeding modes did not affect bioerosion rates but that bioerosion rates were size dependent, with largest individuals (S. rubroviolaceus 45–54 cm FL) bioeroding up to 380 ± 67 kg $ ind^{−1} $ $ year^{−1} $. The size for onset of bioerosion capabilities for both species was 15 cm. Grazing by the two species consumed 60% of the carbonate production of the fore reef area, suggesting that large parrotfishes in Hawaii are ecologically important bioeroders. As individual large S. rubroviolaceus contributed disproportionately more to bioerosion and sediment production than the equivalent biomass of smaller conspecifics, management strategies designed to retain normal reef bioerosion rates should seek to preserve the historical size structure of S. rubroviolaceus populations and to especially protect the larger size classes.
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matchkey_str	article:14321793:2010----::ieoinfoaresywhwiaprofseseisieifrn
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publishDate	2010
allfields	10.1007/s00227-010-1411-y doi (DE-627)SPR002538431 (SPR)s00227-010-1411-y-e DE-627 ger DE-627 rakwb eng Ong, Ling verfasserin aut Bioerosion of coral reefs by two Hawaiian parrotfishes: species, size differences and fishery implications 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 2010 Abstract Parrotfishes can be significant bioeroders and sediment producers on coral reefs. We quantified the bioerosion rates of two similarly sized Hawaiian parrotfishes with two different feeding modes (Scarus rubroviolaceus—a scraper and Chlorurus perspicillatus—an excavator). The results showed that feeding modes did not affect bioerosion rates but that bioerosion rates were size dependent, with largest individuals (S. rubroviolaceus 45–54 cm FL) bioeroding up to 380 ± 67 kg $ ind^{−1} $ $ year^{−1} $. The size for onset of bioerosion capabilities for both species was 15 cm. Grazing by the two species consumed 60% of the carbonate production of the fore reef area, suggesting that large parrotfishes in Hawaii are ecologically important bioeroders. As individual large S. rubroviolaceus contributed disproportionately more to bioerosion and sediment production than the equivalent biomass of smaller conspecifics, management strategies designed to retain normal reef bioerosion rates should seek to preserve the historical size structure of S. rubroviolaceus populations and to especially protect the larger size classes. Fork Length (dpeaa)DE-He213 Fore Reef (dpeaa)DE-He213 Bite Volume (dpeaa)DE-He213 Live Coral (dpeaa)DE-He213 Turf Alga (dpeaa)DE-He213 Holland, Kim N. aut Enthalten in Marine biology Berlin : Springer, 1967 157(2010), 6 vom: 05. März, Seite 1313-1323 (DE-627)25377067X (DE-600)1459413-4 1432-1793 nnns volume:157 year:2010 number:6 day:05 month:03 pages:1313-1323 https://dx.doi.org/10.1007/s00227-010-1411-y 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_206 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_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 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_2056 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_4277 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 157 2010 6 05 03 1313-1323
spelling	10.1007/s00227-010-1411-y doi (DE-627)SPR002538431 (SPR)s00227-010-1411-y-e DE-627 ger DE-627 rakwb eng Ong, Ling verfasserin aut Bioerosion of coral reefs by two Hawaiian parrotfishes: species, size differences and fishery implications 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 2010 Abstract Parrotfishes can be significant bioeroders and sediment producers on coral reefs. We quantified the bioerosion rates of two similarly sized Hawaiian parrotfishes with two different feeding modes (Scarus rubroviolaceus—a scraper and Chlorurus perspicillatus—an excavator). The results showed that feeding modes did not affect bioerosion rates but that bioerosion rates were size dependent, with largest individuals (S. rubroviolaceus 45–54 cm FL) bioeroding up to 380 ± 67 kg $ ind^{−1} $ $ year^{−1} $. The size for onset of bioerosion capabilities for both species was 15 cm. Grazing by the two species consumed 60% of the carbonate production of the fore reef area, suggesting that large parrotfishes in Hawaii are ecologically important bioeroders. As individual large S. rubroviolaceus contributed disproportionately more to bioerosion and sediment production than the equivalent biomass of smaller conspecifics, management strategies designed to retain normal reef bioerosion rates should seek to preserve the historical size structure of S. rubroviolaceus populations and to especially protect the larger size classes. Fork Length (dpeaa)DE-He213 Fore Reef (dpeaa)DE-He213 Bite Volume (dpeaa)DE-He213 Live Coral (dpeaa)DE-He213 Turf Alga (dpeaa)DE-He213 Holland, Kim N. aut Enthalten in Marine biology Berlin : Springer, 1967 157(2010), 6 vom: 05. März, Seite 1313-1323 (DE-627)25377067X (DE-600)1459413-4 1432-1793 nnns volume:157 year:2010 number:6 day:05 month:03 pages:1313-1323 https://dx.doi.org/10.1007/s00227-010-1411-y 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_206 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_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 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_2056 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_4277 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 157 2010 6 05 03 1313-1323
allfields_unstemmed	10.1007/s00227-010-1411-y doi (DE-627)SPR002538431 (SPR)s00227-010-1411-y-e DE-627 ger DE-627 rakwb eng Ong, Ling verfasserin aut Bioerosion of coral reefs by two Hawaiian parrotfishes: species, size differences and fishery implications 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 2010 Abstract Parrotfishes can be significant bioeroders and sediment producers on coral reefs. We quantified the bioerosion rates of two similarly sized Hawaiian parrotfishes with two different feeding modes (Scarus rubroviolaceus—a scraper and Chlorurus perspicillatus—an excavator). The results showed that feeding modes did not affect bioerosion rates but that bioerosion rates were size dependent, with largest individuals (S. rubroviolaceus 45–54 cm FL) bioeroding up to 380 ± 67 kg $ ind^{−1} $ $ year^{−1} $. The size for onset of bioerosion capabilities for both species was 15 cm. Grazing by the two species consumed 60% of the carbonate production of the fore reef area, suggesting that large parrotfishes in Hawaii are ecologically important bioeroders. As individual large S. rubroviolaceus contributed disproportionately more to bioerosion and sediment production than the equivalent biomass of smaller conspecifics, management strategies designed to retain normal reef bioerosion rates should seek to preserve the historical size structure of S. rubroviolaceus populations and to especially protect the larger size classes. Fork Length (dpeaa)DE-He213 Fore Reef (dpeaa)DE-He213 Bite Volume (dpeaa)DE-He213 Live Coral (dpeaa)DE-He213 Turf Alga (dpeaa)DE-He213 Holland, Kim N. aut Enthalten in Marine biology Berlin : Springer, 1967 157(2010), 6 vom: 05. März, Seite 1313-1323 (DE-627)25377067X (DE-600)1459413-4 1432-1793 nnns volume:157 year:2010 number:6 day:05 month:03 pages:1313-1323 https://dx.doi.org/10.1007/s00227-010-1411-y 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_206 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_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 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_2056 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_4277 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 157 2010 6 05 03 1313-1323
allfieldsGer	10.1007/s00227-010-1411-y doi (DE-627)SPR002538431 (SPR)s00227-010-1411-y-e DE-627 ger DE-627 rakwb eng Ong, Ling verfasserin aut Bioerosion of coral reefs by two Hawaiian parrotfishes: species, size differences and fishery implications 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 2010 Abstract Parrotfishes can be significant bioeroders and sediment producers on coral reefs. We quantified the bioerosion rates of two similarly sized Hawaiian parrotfishes with two different feeding modes (Scarus rubroviolaceus—a scraper and Chlorurus perspicillatus—an excavator). The results showed that feeding modes did not affect bioerosion rates but that bioerosion rates were size dependent, with largest individuals (S. rubroviolaceus 45–54 cm FL) bioeroding up to 380 ± 67 kg $ ind^{−1} $ $ year^{−1} $. The size for onset of bioerosion capabilities for both species was 15 cm. Grazing by the two species consumed 60% of the carbonate production of the fore reef area, suggesting that large parrotfishes in Hawaii are ecologically important bioeroders. As individual large S. rubroviolaceus contributed disproportionately more to bioerosion and sediment production than the equivalent biomass of smaller conspecifics, management strategies designed to retain normal reef bioerosion rates should seek to preserve the historical size structure of S. rubroviolaceus populations and to especially protect the larger size classes. Fork Length (dpeaa)DE-He213 Fore Reef (dpeaa)DE-He213 Bite Volume (dpeaa)DE-He213 Live Coral (dpeaa)DE-He213 Turf Alga (dpeaa)DE-He213 Holland, Kim N. aut Enthalten in Marine biology Berlin : Springer, 1967 157(2010), 6 vom: 05. März, Seite 1313-1323 (DE-627)25377067X (DE-600)1459413-4 1432-1793 nnns volume:157 year:2010 number:6 day:05 month:03 pages:1313-1323 https://dx.doi.org/10.1007/s00227-010-1411-y 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_206 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_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 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_2056 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_4277 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 157 2010 6 05 03 1313-1323
allfieldsSound	10.1007/s00227-010-1411-y doi (DE-627)SPR002538431 (SPR)s00227-010-1411-y-e DE-627 ger DE-627 rakwb eng Ong, Ling verfasserin aut Bioerosion of coral reefs by two Hawaiian parrotfishes: species, size differences and fishery implications 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 2010 Abstract Parrotfishes can be significant bioeroders and sediment producers on coral reefs. We quantified the bioerosion rates of two similarly sized Hawaiian parrotfishes with two different feeding modes (Scarus rubroviolaceus—a scraper and Chlorurus perspicillatus—an excavator). The results showed that feeding modes did not affect bioerosion rates but that bioerosion rates were size dependent, with largest individuals (S. rubroviolaceus 45–54 cm FL) bioeroding up to 380 ± 67 kg $ ind^{−1} $ $ year^{−1} $. The size for onset of bioerosion capabilities for both species was 15 cm. Grazing by the two species consumed 60% of the carbonate production of the fore reef area, suggesting that large parrotfishes in Hawaii are ecologically important bioeroders. As individual large S. rubroviolaceus contributed disproportionately more to bioerosion and sediment production than the equivalent biomass of smaller conspecifics, management strategies designed to retain normal reef bioerosion rates should seek to preserve the historical size structure of S. rubroviolaceus populations and to especially protect the larger size classes. Fork Length (dpeaa)DE-He213 Fore Reef (dpeaa)DE-He213 Bite Volume (dpeaa)DE-He213 Live Coral (dpeaa)DE-He213 Turf Alga (dpeaa)DE-He213 Holland, Kim N. aut Enthalten in Marine biology Berlin : Springer, 1967 157(2010), 6 vom: 05. März, Seite 1313-1323 (DE-627)25377067X (DE-600)1459413-4 1432-1793 nnns volume:157 year:2010 number:6 day:05 month:03 pages:1313-1323 https://dx.doi.org/10.1007/s00227-010-1411-y 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_206 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_647 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 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_2056 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_4277 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 157 2010 6 05 03 1313-1323
language	English
source	Enthalten in Marine biology 157(2010), 6 vom: 05. März, Seite 1313-1323 volume:157 year:2010 number:6 day:05 month:03 pages:1313-1323
sourceStr	Enthalten in Marine biology 157(2010), 6 vom: 05. März, Seite 1313-1323 volume:157 year:2010 number:6 day:05 month:03 pages:1313-1323
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	Fork Length Fore Reef Bite Volume Live Coral Turf Alga
isfreeaccess_bool	false
container_title	Marine biology
authorswithroles_txt_mv	Ong, Ling @@aut@@ Holland, Kim N. @@aut@@
publishDateDaySort_date	2010-03-05T00:00:00Z
hierarchy_top_id	25377067X
id	SPR002538431
language_de	englisch
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author	Ong, Ling
spellingShingle	Ong, Ling misc Fork Length misc Fore Reef misc Bite Volume misc Live Coral misc Turf Alga Bioerosion of coral reefs by two Hawaiian parrotfishes: species, size differences and fishery implications
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topic_title	Bioerosion of coral reefs by two Hawaiian parrotfishes: species, size differences and fishery implications Fork Length (dpeaa)DE-He213 Fore Reef (dpeaa)DE-He213 Bite Volume (dpeaa)DE-He213 Live Coral (dpeaa)DE-He213 Turf Alga (dpeaa)DE-He213
topic	misc Fork Length misc Fore Reef misc Bite Volume misc Live Coral misc Turf Alga
topic_unstemmed	misc Fork Length misc Fore Reef misc Bite Volume misc Live Coral misc Turf Alga
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title	Bioerosion of coral reefs by two Hawaiian parrotfishes: species, size differences and fishery implications
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title_full	Bioerosion of coral reefs by two Hawaiian parrotfishes: species, size differences and fishery implications
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author_browse	Ong, Ling Holland, Kim N.
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doi_str_mv	10.1007/s00227-010-1411-y
title_sort	bioerosion of coral reefs by two hawaiian parrotfishes: species, size differences and fishery implications
title_auth	Bioerosion of coral reefs by two Hawaiian parrotfishes: species, size differences and fishery implications
abstract	Abstract Parrotfishes can be significant bioeroders and sediment producers on coral reefs. We quantified the bioerosion rates of two similarly sized Hawaiian parrotfishes with two different feeding modes (Scarus rubroviolaceus—a scraper and Chlorurus perspicillatus—an excavator). The results showed that feeding modes did not affect bioerosion rates but that bioerosion rates were size dependent, with largest individuals (S. rubroviolaceus 45–54 cm FL) bioeroding up to 380 ± 67 kg $ ind^{−1} $ $ year^{−1} $. The size for onset of bioerosion capabilities for both species was 15 cm. Grazing by the two species consumed 60% of the carbonate production of the fore reef area, suggesting that large parrotfishes in Hawaii are ecologically important bioeroders. As individual large S. rubroviolaceus contributed disproportionately more to bioerosion and sediment production than the equivalent biomass of smaller conspecifics, management strategies designed to retain normal reef bioerosion rates should seek to preserve the historical size structure of S. rubroviolaceus populations and to especially protect the larger size classes. © Springer-Verlag 2010
abstractGer	Abstract Parrotfishes can be significant bioeroders and sediment producers on coral reefs. We quantified the bioerosion rates of two similarly sized Hawaiian parrotfishes with two different feeding modes (Scarus rubroviolaceus—a scraper and Chlorurus perspicillatus—an excavator). The results showed that feeding modes did not affect bioerosion rates but that bioerosion rates were size dependent, with largest individuals (S. rubroviolaceus 45–54 cm FL) bioeroding up to 380 ± 67 kg $ ind^{−1} $ $ year^{−1} $. The size for onset of bioerosion capabilities for both species was 15 cm. Grazing by the two species consumed 60% of the carbonate production of the fore reef area, suggesting that large parrotfishes in Hawaii are ecologically important bioeroders. As individual large S. rubroviolaceus contributed disproportionately more to bioerosion and sediment production than the equivalent biomass of smaller conspecifics, management strategies designed to retain normal reef bioerosion rates should seek to preserve the historical size structure of S. rubroviolaceus populations and to especially protect the larger size classes. © Springer-Verlag 2010
abstract_unstemmed	Abstract Parrotfishes can be significant bioeroders and sediment producers on coral reefs. We quantified the bioerosion rates of two similarly sized Hawaiian parrotfishes with two different feeding modes (Scarus rubroviolaceus—a scraper and Chlorurus perspicillatus—an excavator). The results showed that feeding modes did not affect bioerosion rates but that bioerosion rates were size dependent, with largest individuals (S. rubroviolaceus 45–54 cm FL) bioeroding up to 380 ± 67 kg $ ind^{−1} $ $ year^{−1} $. The size for onset of bioerosion capabilities for both species was 15 cm. Grazing by the two species consumed 60% of the carbonate production of the fore reef area, suggesting that large parrotfishes in Hawaii are ecologically important bioeroders. As individual large S. rubroviolaceus contributed disproportionately more to bioerosion and sediment production than the equivalent biomass of smaller conspecifics, management strategies designed to retain normal reef bioerosion rates should seek to preserve the historical size structure of S. rubroviolaceus populations and to especially protect the larger size classes. © Springer-Verlag 2010
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container_issue	6
title_short	Bioerosion of coral reefs by two Hawaiian parrotfishes: species, size differences and fishery implications
url	https://dx.doi.org/10.1007/s00227-010-1411-y
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Bioerosion of coral reefs by two Hawaiian parrotfishes: species, size differences and fishery implications

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