Interactions between the brown tide-causing microalga Aureococcus anophagefferens and the small diatom Minutocellus polymorphus under laboratory culture

Abstract Brown tides caused by Aureococcus anophagefferens (Pelagophyta) have broken out frequently and have caused serious ecological problems in the coastal waters of the Bohai Sea, China, since 2009. During the brown tides caused by A. anophagefferens, the small marine diatom Minutocellus polymor...
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Autor*in:	Chen, Yanghang [verfasserIn] Gao, Yahui [verfasserIn] Chen, Changping [verfasserIn] Li, Xuesong [verfasserIn] Liang, Junrong [verfasserIn] Sun, Lin [verfasserIn] Wang, Yingyue [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2018

Schlagwörter:	Allelopathy Brown tide Succession

Übergeordnetes Werk:	Enthalten in: Journal of applied phycology - Dordrecht [u.a.] : Springer Science + Business Media B.V, 1989, 31(2018), 3 vom: 18. Dez., Seite 1793-1803
Übergeordnetes Werk:	volume:31 ; year:2018 ; number:3 ; day:18 ; month:12 ; pages:1793-1803

Links:	Volltext

DOI / URN:	10.1007/s10811-018-1704-y

Katalog-ID:	SPR013488783

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520			\|a Abstract Brown tides caused by Aureococcus anophagefferens (Pelagophyta) have broken out frequently and have caused serious ecological problems in the coastal waters of the Bohai Sea, China, since 2009. During the brown tides caused by A. anophagefferens, the small marine diatom Minutocellus polymorphus has often become dominant, co-existing with A. anophagefferens. To investigate the bloom formation mechanisms and co-existence factors involved, bi-algal culture and growth experiments with culture filtrates were performed under laboratory-controlled conditions. In our experiments, A. anophagefferens and M. polymorphus growth was allelopathically suppressed by the other species, depending on initial cell densities and growth stages; however, the species did not outcompete each other during the observed time frame. The results also suggested that the relevant allelochemicals might be a mixture containing some temperature-sensitive compounds. Growth simulation performed via the Lotka-Volterra model indicated that the initial cell density of these two species was critical in determining their growth and competition in bi-algal culture. Our results showed that a similar allelopathic effect was exerted by A. anophagefferens on M. polymorphus and vice versa. This effect could be important in allowing the observed co-existence of these two species in natural waters during brown tides.
650		4	\|a Allelopathy \|7 (dpeaa)DE-He213
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700	1		\|a Liang, Junrong \|e verfasserin \|4 aut
700	1		\|a Sun, Lin \|e verfasserin \|4 aut
700	1		\|a Wang, Yingyue \|e verfasserin \|4 aut
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author_variant	y c yc y g yg c c cc x l xl j l jl l s ls y w yw
matchkey_str	article:15735176:2018----::neatoseweterwtdcuigiragaroocsnpaefrnadhsalitmiuoe
hierarchy_sort_str	2018
bklnumber	42.00
publishDate	2018
allfields	10.1007/s10811-018-1704-y doi (DE-627)SPR013488783 (SPR)s10811-018-1704-y-e DE-627 ger DE-627 rakwb eng 580 570 ASE 42.00 bkl Chen, Yanghang verfasserin aut Interactions between the brown tide-causing microalga Aureococcus anophagefferens and the small diatom Minutocellus polymorphus under laboratory culture 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Brown tides caused by Aureococcus anophagefferens (Pelagophyta) have broken out frequently and have caused serious ecological problems in the coastal waters of the Bohai Sea, China, since 2009. During the brown tides caused by A. anophagefferens, the small marine diatom Minutocellus polymorphus has often become dominant, co-existing with A. anophagefferens. To investigate the bloom formation mechanisms and co-existence factors involved, bi-algal culture and growth experiments with culture filtrates were performed under laboratory-controlled conditions. In our experiments, A. anophagefferens and M. polymorphus growth was allelopathically suppressed by the other species, depending on initial cell densities and growth stages; however, the species did not outcompete each other during the observed time frame. The results also suggested that the relevant allelochemicals might be a mixture containing some temperature-sensitive compounds. Growth simulation performed via the Lotka-Volterra model indicated that the initial cell density of these two species was critical in determining their growth and competition in bi-algal culture. Our results showed that a similar allelopathic effect was exerted by A. anophagefferens on M. polymorphus and vice versa. This effect could be important in allowing the observed co-existence of these two species in natural waters during brown tides. Allelopathy (dpeaa)DE-He213 Brown tide (dpeaa)DE-He213 Succession (dpeaa)DE-He213 Gao, Yahui verfasserin aut Chen, Changping verfasserin aut Li, Xuesong verfasserin aut Liang, Junrong verfasserin aut Sun, Lin verfasserin aut Wang, Yingyue verfasserin aut Enthalten in Journal of applied phycology Dordrecht [u.a.] : Springer Science + Business Media B.V, 1989 31(2018), 3 vom: 18. Dez., Seite 1793-1803 (DE-627)270429980 (DE-600)1477703-4 1573-5176 nnns volume:31 year:2018 number:3 day:18 month:12 pages:1793-1803 https://dx.doi.org/10.1007/s10811-018-1704-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_101 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_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_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_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_2360 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 42.00 ASE AR 31 2018 3 18 12 1793-1803
spelling	10.1007/s10811-018-1704-y doi (DE-627)SPR013488783 (SPR)s10811-018-1704-y-e DE-627 ger DE-627 rakwb eng 580 570 ASE 42.00 bkl Chen, Yanghang verfasserin aut Interactions between the brown tide-causing microalga Aureococcus anophagefferens and the small diatom Minutocellus polymorphus under laboratory culture 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Brown tides caused by Aureococcus anophagefferens (Pelagophyta) have broken out frequently and have caused serious ecological problems in the coastal waters of the Bohai Sea, China, since 2009. During the brown tides caused by A. anophagefferens, the small marine diatom Minutocellus polymorphus has often become dominant, co-existing with A. anophagefferens. To investigate the bloom formation mechanisms and co-existence factors involved, bi-algal culture and growth experiments with culture filtrates were performed under laboratory-controlled conditions. In our experiments, A. anophagefferens and M. polymorphus growth was allelopathically suppressed by the other species, depending on initial cell densities and growth stages; however, the species did not outcompete each other during the observed time frame. The results also suggested that the relevant allelochemicals might be a mixture containing some temperature-sensitive compounds. Growth simulation performed via the Lotka-Volterra model indicated that the initial cell density of these two species was critical in determining their growth and competition in bi-algal culture. Our results showed that a similar allelopathic effect was exerted by A. anophagefferens on M. polymorphus and vice versa. This effect could be important in allowing the observed co-existence of these two species in natural waters during brown tides. Allelopathy (dpeaa)DE-He213 Brown tide (dpeaa)DE-He213 Succession (dpeaa)DE-He213 Gao, Yahui verfasserin aut Chen, Changping verfasserin aut Li, Xuesong verfasserin aut Liang, Junrong verfasserin aut Sun, Lin verfasserin aut Wang, Yingyue verfasserin aut Enthalten in Journal of applied phycology Dordrecht [u.a.] : Springer Science + Business Media B.V, 1989 31(2018), 3 vom: 18. Dez., Seite 1793-1803 (DE-627)270429980 (DE-600)1477703-4 1573-5176 nnns volume:31 year:2018 number:3 day:18 month:12 pages:1793-1803 https://dx.doi.org/10.1007/s10811-018-1704-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_101 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_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_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_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_2360 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 42.00 ASE AR 31 2018 3 18 12 1793-1803
allfields_unstemmed	10.1007/s10811-018-1704-y doi (DE-627)SPR013488783 (SPR)s10811-018-1704-y-e DE-627 ger DE-627 rakwb eng 580 570 ASE 42.00 bkl Chen, Yanghang verfasserin aut Interactions between the brown tide-causing microalga Aureococcus anophagefferens and the small diatom Minutocellus polymorphus under laboratory culture 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Brown tides caused by Aureococcus anophagefferens (Pelagophyta) have broken out frequently and have caused serious ecological problems in the coastal waters of the Bohai Sea, China, since 2009. During the brown tides caused by A. anophagefferens, the small marine diatom Minutocellus polymorphus has often become dominant, co-existing with A. anophagefferens. To investigate the bloom formation mechanisms and co-existence factors involved, bi-algal culture and growth experiments with culture filtrates were performed under laboratory-controlled conditions. In our experiments, A. anophagefferens and M. polymorphus growth was allelopathically suppressed by the other species, depending on initial cell densities and growth stages; however, the species did not outcompete each other during the observed time frame. The results also suggested that the relevant allelochemicals might be a mixture containing some temperature-sensitive compounds. Growth simulation performed via the Lotka-Volterra model indicated that the initial cell density of these two species was critical in determining their growth and competition in bi-algal culture. Our results showed that a similar allelopathic effect was exerted by A. anophagefferens on M. polymorphus and vice versa. This effect could be important in allowing the observed co-existence of these two species in natural waters during brown tides. Allelopathy (dpeaa)DE-He213 Brown tide (dpeaa)DE-He213 Succession (dpeaa)DE-He213 Gao, Yahui verfasserin aut Chen, Changping verfasserin aut Li, Xuesong verfasserin aut Liang, Junrong verfasserin aut Sun, Lin verfasserin aut Wang, Yingyue verfasserin aut Enthalten in Journal of applied phycology Dordrecht [u.a.] : Springer Science + Business Media B.V, 1989 31(2018), 3 vom: 18. Dez., Seite 1793-1803 (DE-627)270429980 (DE-600)1477703-4 1573-5176 nnns volume:31 year:2018 number:3 day:18 month:12 pages:1793-1803 https://dx.doi.org/10.1007/s10811-018-1704-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_101 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_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_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_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_2360 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 42.00 ASE AR 31 2018 3 18 12 1793-1803
allfieldsGer	10.1007/s10811-018-1704-y doi (DE-627)SPR013488783 (SPR)s10811-018-1704-y-e DE-627 ger DE-627 rakwb eng 580 570 ASE 42.00 bkl Chen, Yanghang verfasserin aut Interactions between the brown tide-causing microalga Aureococcus anophagefferens and the small diatom Minutocellus polymorphus under laboratory culture 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Brown tides caused by Aureococcus anophagefferens (Pelagophyta) have broken out frequently and have caused serious ecological problems in the coastal waters of the Bohai Sea, China, since 2009. During the brown tides caused by A. anophagefferens, the small marine diatom Minutocellus polymorphus has often become dominant, co-existing with A. anophagefferens. To investigate the bloom formation mechanisms and co-existence factors involved, bi-algal culture and growth experiments with culture filtrates were performed under laboratory-controlled conditions. In our experiments, A. anophagefferens and M. polymorphus growth was allelopathically suppressed by the other species, depending on initial cell densities and growth stages; however, the species did not outcompete each other during the observed time frame. The results also suggested that the relevant allelochemicals might be a mixture containing some temperature-sensitive compounds. Growth simulation performed via the Lotka-Volterra model indicated that the initial cell density of these two species was critical in determining their growth and competition in bi-algal culture. Our results showed that a similar allelopathic effect was exerted by A. anophagefferens on M. polymorphus and vice versa. This effect could be important in allowing the observed co-existence of these two species in natural waters during brown tides. Allelopathy (dpeaa)DE-He213 Brown tide (dpeaa)DE-He213 Succession (dpeaa)DE-He213 Gao, Yahui verfasserin aut Chen, Changping verfasserin aut Li, Xuesong verfasserin aut Liang, Junrong verfasserin aut Sun, Lin verfasserin aut Wang, Yingyue verfasserin aut Enthalten in Journal of applied phycology Dordrecht [u.a.] : Springer Science + Business Media B.V, 1989 31(2018), 3 vom: 18. Dez., Seite 1793-1803 (DE-627)270429980 (DE-600)1477703-4 1573-5176 nnns volume:31 year:2018 number:3 day:18 month:12 pages:1793-1803 https://dx.doi.org/10.1007/s10811-018-1704-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_101 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_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_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_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_2360 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 42.00 ASE AR 31 2018 3 18 12 1793-1803
allfieldsSound	10.1007/s10811-018-1704-y doi (DE-627)SPR013488783 (SPR)s10811-018-1704-y-e DE-627 ger DE-627 rakwb eng 580 570 ASE 42.00 bkl Chen, Yanghang verfasserin aut Interactions between the brown tide-causing microalga Aureococcus anophagefferens and the small diatom Minutocellus polymorphus under laboratory culture 2018 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Brown tides caused by Aureococcus anophagefferens (Pelagophyta) have broken out frequently and have caused serious ecological problems in the coastal waters of the Bohai Sea, China, since 2009. During the brown tides caused by A. anophagefferens, the small marine diatom Minutocellus polymorphus has often become dominant, co-existing with A. anophagefferens. To investigate the bloom formation mechanisms and co-existence factors involved, bi-algal culture and growth experiments with culture filtrates were performed under laboratory-controlled conditions. In our experiments, A. anophagefferens and M. polymorphus growth was allelopathically suppressed by the other species, depending on initial cell densities and growth stages; however, the species did not outcompete each other during the observed time frame. The results also suggested that the relevant allelochemicals might be a mixture containing some temperature-sensitive compounds. Growth simulation performed via the Lotka-Volterra model indicated that the initial cell density of these two species was critical in determining their growth and competition in bi-algal culture. Our results showed that a similar allelopathic effect was exerted by A. anophagefferens on M. polymorphus and vice versa. This effect could be important in allowing the observed co-existence of these two species in natural waters during brown tides. Allelopathy (dpeaa)DE-He213 Brown tide (dpeaa)DE-He213 Succession (dpeaa)DE-He213 Gao, Yahui verfasserin aut Chen, Changping verfasserin aut Li, Xuesong verfasserin aut Liang, Junrong verfasserin aut Sun, Lin verfasserin aut Wang, Yingyue verfasserin aut Enthalten in Journal of applied phycology Dordrecht [u.a.] : Springer Science + Business Media B.V, 1989 31(2018), 3 vom: 18. Dez., Seite 1793-1803 (DE-627)270429980 (DE-600)1477703-4 1573-5176 nnns volume:31 year:2018 number:3 day:18 month:12 pages:1793-1803 https://dx.doi.org/10.1007/s10811-018-1704-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA 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_101 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_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_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_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_2360 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 42.00 ASE AR 31 2018 3 18 12 1793-1803
language	English
source	Enthalten in Journal of applied phycology 31(2018), 3 vom: 18. Dez., Seite 1793-1803 volume:31 year:2018 number:3 day:18 month:12 pages:1793-1803
sourceStr	Enthalten in Journal of applied phycology 31(2018), 3 vom: 18. Dez., Seite 1793-1803 volume:31 year:2018 number:3 day:18 month:12 pages:1793-1803
format_phy_str_mv	Article
institution	findex.gbv.de
topic_facet	Allelopathy Brown tide Succession
dewey-raw	580
isfreeaccess_bool	false
container_title	Journal of applied phycology
authorswithroles_txt_mv	Chen, Yanghang @@aut@@ Gao, Yahui @@aut@@ Chen, Changping @@aut@@ Li, Xuesong @@aut@@ Liang, Junrong @@aut@@ Sun, Lin @@aut@@ Wang, Yingyue @@aut@@
publishDateDaySort_date	2018-12-18T00:00:00Z
hierarchy_top_id	270429980
dewey-sort	3580
id	SPR013488783
language_de	englisch
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author	Chen, Yanghang
spellingShingle	Chen, Yanghang ddc 580 bkl 42.00 misc Allelopathy misc Brown tide misc Succession Interactions between the brown tide-causing microalga Aureococcus anophagefferens and the small diatom Minutocellus polymorphus under laboratory culture
authorStr	Chen, Yanghang
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topic_title	580 570 ASE 42.00 bkl Interactions between the brown tide-causing microalga Aureococcus anophagefferens and the small diatom Minutocellus polymorphus under laboratory culture Allelopathy (dpeaa)DE-He213 Brown tide (dpeaa)DE-He213 Succession (dpeaa)DE-He213
topic	ddc 580 bkl 42.00 misc Allelopathy misc Brown tide misc Succession
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title	Interactions between the brown tide-causing microalga Aureococcus anophagefferens and the small diatom Minutocellus polymorphus under laboratory culture
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title_full	Interactions between the brown tide-causing microalga Aureococcus anophagefferens and the small diatom Minutocellus polymorphus under laboratory culture
author_sort	Chen, Yanghang
journal	Journal of applied phycology
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author_browse	Chen, Yanghang Gao, Yahui Chen, Changping Li, Xuesong Liang, Junrong Sun, Lin Wang, Yingyue
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title_sort	interactions between the brown tide-causing microalga aureococcus anophagefferens and the small diatom minutocellus polymorphus under laboratory culture
title_auth	Interactions between the brown tide-causing microalga Aureococcus anophagefferens and the small diatom Minutocellus polymorphus under laboratory culture
abstract	Abstract Brown tides caused by Aureococcus anophagefferens (Pelagophyta) have broken out frequently and have caused serious ecological problems in the coastal waters of the Bohai Sea, China, since 2009. During the brown tides caused by A. anophagefferens, the small marine diatom Minutocellus polymorphus has often become dominant, co-existing with A. anophagefferens. To investigate the bloom formation mechanisms and co-existence factors involved, bi-algal culture and growth experiments with culture filtrates were performed under laboratory-controlled conditions. In our experiments, A. anophagefferens and M. polymorphus growth was allelopathically suppressed by the other species, depending on initial cell densities and growth stages; however, the species did not outcompete each other during the observed time frame. The results also suggested that the relevant allelochemicals might be a mixture containing some temperature-sensitive compounds. Growth simulation performed via the Lotka-Volterra model indicated that the initial cell density of these two species was critical in determining their growth and competition in bi-algal culture. Our results showed that a similar allelopathic effect was exerted by A. anophagefferens on M. polymorphus and vice versa. This effect could be important in allowing the observed co-existence of these two species in natural waters during brown tides.
abstractGer	Abstract Brown tides caused by Aureococcus anophagefferens (Pelagophyta) have broken out frequently and have caused serious ecological problems in the coastal waters of the Bohai Sea, China, since 2009. During the brown tides caused by A. anophagefferens, the small marine diatom Minutocellus polymorphus has often become dominant, co-existing with A. anophagefferens. To investigate the bloom formation mechanisms and co-existence factors involved, bi-algal culture and growth experiments with culture filtrates were performed under laboratory-controlled conditions. In our experiments, A. anophagefferens and M. polymorphus growth was allelopathically suppressed by the other species, depending on initial cell densities and growth stages; however, the species did not outcompete each other during the observed time frame. The results also suggested that the relevant allelochemicals might be a mixture containing some temperature-sensitive compounds. Growth simulation performed via the Lotka-Volterra model indicated that the initial cell density of these two species was critical in determining their growth and competition in bi-algal culture. Our results showed that a similar allelopathic effect was exerted by A. anophagefferens on M. polymorphus and vice versa. This effect could be important in allowing the observed co-existence of these two species in natural waters during brown tides.
abstract_unstemmed	Abstract Brown tides caused by Aureococcus anophagefferens (Pelagophyta) have broken out frequently and have caused serious ecological problems in the coastal waters of the Bohai Sea, China, since 2009. During the brown tides caused by A. anophagefferens, the small marine diatom Minutocellus polymorphus has often become dominant, co-existing with A. anophagefferens. To investigate the bloom formation mechanisms and co-existence factors involved, bi-algal culture and growth experiments with culture filtrates were performed under laboratory-controlled conditions. In our experiments, A. anophagefferens and M. polymorphus growth was allelopathically suppressed by the other species, depending on initial cell densities and growth stages; however, the species did not outcompete each other during the observed time frame. The results also suggested that the relevant allelochemicals might be a mixture containing some temperature-sensitive compounds. Growth simulation performed via the Lotka-Volterra model indicated that the initial cell density of these two species was critical in determining their growth and competition in bi-algal culture. Our results showed that a similar allelopathic effect was exerted by A. anophagefferens on M. polymorphus and vice versa. This effect could be important in allowing the observed co-existence of these two species in natural waters during brown tides.
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container_issue	3
title_short	Interactions between the brown tide-causing microalga Aureococcus anophagefferens and the small diatom Minutocellus polymorphus under laboratory culture
url	https://dx.doi.org/10.1007/s10811-018-1704-y
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author2	Gao, Yahui Chen, Changping Li, Xuesong Liang, Junrong Sun, Lin Wang, Yingyue
author2Str	Gao, Yahui Chen, Changping Li, Xuesong Liang, Junrong Sun, Lin Wang, Yingyue
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doi_str	10.1007/s10811-018-1704-y
up_date	2024-07-03T20:04:44.905Z
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Interactions between the brown tide-causing microalga Aureococcus anophagefferens and the small diatom Minutocellus polymorphus under laboratory culture

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