Gas exchange and photosynthetic performance of the tropical tree Acacia nigrescens when grown in different $ CO_{2} $ concentrations
Abstract The photosynthetic responses of the tropical tree species Acacia nigrescens Oliv. grown at different atmospheric $ CO_{2} $ concentrations—from sub-ambient to super-ambient—have been studied. Light-saturated rates of net photosynthesis (Asat) in A. nigrescens, measured after 120 days exposu...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Possell, Malcolm [verfasserIn] Nicholas Hewitt, C. [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2009 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Planta - Berlin : Springer, 1925, 229(2009), 4 vom: 04. Jan., Seite 837-846 |
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| Übergeordnetes Werk: |
volume:229 ; year:2009 ; number:4 ; day:04 ; month:01 ; pages:837-846 |
| Links: |
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| DOI / URN: |
10.1007/s00425-008-0883-1 |
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| Katalog-ID: |
SPR005656869 |
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| 100 | 1 | |a Possell, Malcolm |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Gas exchange and photosynthetic performance of the tropical tree Acacia nigrescens when grown in different $ CO_{2} $ concentrations |
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| 520 | |a Abstract The photosynthetic responses of the tropical tree species Acacia nigrescens Oliv. grown at different atmospheric $ CO_{2} $ concentrations—from sub-ambient to super-ambient—have been studied. Light-saturated rates of net photosynthesis (Asat) in A. nigrescens, measured after 120 days exposure, increased significantly from sub-ambient (196 μL $ L^{−1} $) to current ambient (386 μL $ L^{−1} $) $ CO_{2} $ growth conditions but did not increase any further as [$ CO_{2} $] became super-ambient (597 μL $ L^{−1} $). Examination of photosynthetic $ CO_{2} $ response curves, leaf nitrogen content, and leaf thickness showed that this acclimation was most likely caused by reduction in Rubisco activity and a shift towards ribulose-1,5-bisphosphate regeneration-limited photosynthesis, but not a consequence of changes in mesophyll conductance. Also, measurements of the maximum efficiency of PSII and the carotenoid to chlorophyll ratio of leaves indicated that it was unlikely that the pattern of Asat seen was a consequence of growth [$ CO_{2} $] induced stress. Many of the photosynthetic responses examined were not linear with respect to the concentration of $ CO_{2} $ but could be explained by current models of photosynthesis. | ||
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| 650 | 4 | |a Nitrogen content |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Photosynthesis |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Sub-ambient CO |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Water-use efficiency |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Nicholas Hewitt, C. |e verfasserin |4 aut | |
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10.1007/s00425-008-0883-1 doi (DE-627)SPR005656869 (SPR)s00425-008-0883-1-e DE-627 ger DE-627 rakwb eng 580 ASE 42.38 bkl Possell, Malcolm verfasserin aut Gas exchange and photosynthetic performance of the tropical tree Acacia nigrescens when grown in different $ CO_{2} $ concentrations 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The photosynthetic responses of the tropical tree species Acacia nigrescens Oliv. grown at different atmospheric $ CO_{2} $ concentrations—from sub-ambient to super-ambient—have been studied. Light-saturated rates of net photosynthesis (Asat) in A. nigrescens, measured after 120 days exposure, increased significantly from sub-ambient (196 μL $ L^{−1} $) to current ambient (386 μL $ L^{−1} $) $ CO_{2} $ growth conditions but did not increase any further as [$ CO_{2} $] became super-ambient (597 μL $ L^{−1} $). Examination of photosynthetic $ CO_{2} $ response curves, leaf nitrogen content, and leaf thickness showed that this acclimation was most likely caused by reduction in Rubisco activity and a shift towards ribulose-1,5-bisphosphate regeneration-limited photosynthesis, but not a consequence of changes in mesophyll conductance. Also, measurements of the maximum efficiency of PSII and the carotenoid to chlorophyll ratio of leaves indicated that it was unlikely that the pattern of Asat seen was a consequence of growth [$ CO_{2} $] induced stress. Many of the photosynthetic responses examined were not linear with respect to the concentration of $ CO_{2} $ but could be explained by current models of photosynthesis. Elevated CO (dpeaa)DE-He213 Nitrogen content (dpeaa)DE-He213 Photosynthesis (dpeaa)DE-He213 Sub-ambient CO (dpeaa)DE-He213 Water-use efficiency (dpeaa)DE-He213 Nicholas Hewitt, C. verfasserin aut Enthalten in Planta Berlin : Springer, 1925 229(2009), 4 vom: 04. Jan., Seite 837-846 (DE-627)254639100 (DE-600)1463030-8 1432-2048 nnns volume:229 year:2009 number:4 day:04 month:01 pages:837-846 https://dx.doi.org/10.1007/s00425-008-0883-1 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_65 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_374 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_2018 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_2946 GBV_ILN_2949 GBV_ILN_2951 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 42.38 ASE AR 229 2009 4 04 01 837-846 |
| spelling |
10.1007/s00425-008-0883-1 doi (DE-627)SPR005656869 (SPR)s00425-008-0883-1-e DE-627 ger DE-627 rakwb eng 580 ASE 42.38 bkl Possell, Malcolm verfasserin aut Gas exchange and photosynthetic performance of the tropical tree Acacia nigrescens when grown in different $ CO_{2} $ concentrations 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The photosynthetic responses of the tropical tree species Acacia nigrescens Oliv. grown at different atmospheric $ CO_{2} $ concentrations—from sub-ambient to super-ambient—have been studied. Light-saturated rates of net photosynthesis (Asat) in A. nigrescens, measured after 120 days exposure, increased significantly from sub-ambient (196 μL $ L^{−1} $) to current ambient (386 μL $ L^{−1} $) $ CO_{2} $ growth conditions but did not increase any further as [$ CO_{2} $] became super-ambient (597 μL $ L^{−1} $). Examination of photosynthetic $ CO_{2} $ response curves, leaf nitrogen content, and leaf thickness showed that this acclimation was most likely caused by reduction in Rubisco activity and a shift towards ribulose-1,5-bisphosphate regeneration-limited photosynthesis, but not a consequence of changes in mesophyll conductance. Also, measurements of the maximum efficiency of PSII and the carotenoid to chlorophyll ratio of leaves indicated that it was unlikely that the pattern of Asat seen was a consequence of growth [$ CO_{2} $] induced stress. Many of the photosynthetic responses examined were not linear with respect to the concentration of $ CO_{2} $ but could be explained by current models of photosynthesis. Elevated CO (dpeaa)DE-He213 Nitrogen content (dpeaa)DE-He213 Photosynthesis (dpeaa)DE-He213 Sub-ambient CO (dpeaa)DE-He213 Water-use efficiency (dpeaa)DE-He213 Nicholas Hewitt, C. verfasserin aut Enthalten in Planta Berlin : Springer, 1925 229(2009), 4 vom: 04. Jan., Seite 837-846 (DE-627)254639100 (DE-600)1463030-8 1432-2048 nnns volume:229 year:2009 number:4 day:04 month:01 pages:837-846 https://dx.doi.org/10.1007/s00425-008-0883-1 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_65 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_374 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_2018 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_2946 GBV_ILN_2949 GBV_ILN_2951 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 42.38 ASE AR 229 2009 4 04 01 837-846 |
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10.1007/s00425-008-0883-1 doi (DE-627)SPR005656869 (SPR)s00425-008-0883-1-e DE-627 ger DE-627 rakwb eng 580 ASE 42.38 bkl Possell, Malcolm verfasserin aut Gas exchange and photosynthetic performance of the tropical tree Acacia nigrescens when grown in different $ CO_{2} $ concentrations 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The photosynthetic responses of the tropical tree species Acacia nigrescens Oliv. grown at different atmospheric $ CO_{2} $ concentrations—from sub-ambient to super-ambient—have been studied. Light-saturated rates of net photosynthesis (Asat) in A. nigrescens, measured after 120 days exposure, increased significantly from sub-ambient (196 μL $ L^{−1} $) to current ambient (386 μL $ L^{−1} $) $ CO_{2} $ growth conditions but did not increase any further as [$ CO_{2} $] became super-ambient (597 μL $ L^{−1} $). Examination of photosynthetic $ CO_{2} $ response curves, leaf nitrogen content, and leaf thickness showed that this acclimation was most likely caused by reduction in Rubisco activity and a shift towards ribulose-1,5-bisphosphate regeneration-limited photosynthesis, but not a consequence of changes in mesophyll conductance. Also, measurements of the maximum efficiency of PSII and the carotenoid to chlorophyll ratio of leaves indicated that it was unlikely that the pattern of Asat seen was a consequence of growth [$ CO_{2} $] induced stress. Many of the photosynthetic responses examined were not linear with respect to the concentration of $ CO_{2} $ but could be explained by current models of photosynthesis. Elevated CO (dpeaa)DE-He213 Nitrogen content (dpeaa)DE-He213 Photosynthesis (dpeaa)DE-He213 Sub-ambient CO (dpeaa)DE-He213 Water-use efficiency (dpeaa)DE-He213 Nicholas Hewitt, C. verfasserin aut Enthalten in Planta Berlin : Springer, 1925 229(2009), 4 vom: 04. Jan., Seite 837-846 (DE-627)254639100 (DE-600)1463030-8 1432-2048 nnns volume:229 year:2009 number:4 day:04 month:01 pages:837-846 https://dx.doi.org/10.1007/s00425-008-0883-1 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_65 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_374 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_2018 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_2946 GBV_ILN_2949 GBV_ILN_2951 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 42.38 ASE AR 229 2009 4 04 01 837-846 |
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10.1007/s00425-008-0883-1 doi (DE-627)SPR005656869 (SPR)s00425-008-0883-1-e DE-627 ger DE-627 rakwb eng 580 ASE 42.38 bkl Possell, Malcolm verfasserin aut Gas exchange and photosynthetic performance of the tropical tree Acacia nigrescens when grown in different $ CO_{2} $ concentrations 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The photosynthetic responses of the tropical tree species Acacia nigrescens Oliv. grown at different atmospheric $ CO_{2} $ concentrations—from sub-ambient to super-ambient—have been studied. Light-saturated rates of net photosynthesis (Asat) in A. nigrescens, measured after 120 days exposure, increased significantly from sub-ambient (196 μL $ L^{−1} $) to current ambient (386 μL $ L^{−1} $) $ CO_{2} $ growth conditions but did not increase any further as [$ CO_{2} $] became super-ambient (597 μL $ L^{−1} $). Examination of photosynthetic $ CO_{2} $ response curves, leaf nitrogen content, and leaf thickness showed that this acclimation was most likely caused by reduction in Rubisco activity and a shift towards ribulose-1,5-bisphosphate regeneration-limited photosynthesis, but not a consequence of changes in mesophyll conductance. Also, measurements of the maximum efficiency of PSII and the carotenoid to chlorophyll ratio of leaves indicated that it was unlikely that the pattern of Asat seen was a consequence of growth [$ CO_{2} $] induced stress. Many of the photosynthetic responses examined were not linear with respect to the concentration of $ CO_{2} $ but could be explained by current models of photosynthesis. Elevated CO (dpeaa)DE-He213 Nitrogen content (dpeaa)DE-He213 Photosynthesis (dpeaa)DE-He213 Sub-ambient CO (dpeaa)DE-He213 Water-use efficiency (dpeaa)DE-He213 Nicholas Hewitt, C. verfasserin aut Enthalten in Planta Berlin : Springer, 1925 229(2009), 4 vom: 04. Jan., Seite 837-846 (DE-627)254639100 (DE-600)1463030-8 1432-2048 nnns volume:229 year:2009 number:4 day:04 month:01 pages:837-846 https://dx.doi.org/10.1007/s00425-008-0883-1 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_65 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_374 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_2018 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_2946 GBV_ILN_2949 GBV_ILN_2951 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 42.38 ASE AR 229 2009 4 04 01 837-846 |
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10.1007/s00425-008-0883-1 doi (DE-627)SPR005656869 (SPR)s00425-008-0883-1-e DE-627 ger DE-627 rakwb eng 580 ASE 42.38 bkl Possell, Malcolm verfasserin aut Gas exchange and photosynthetic performance of the tropical tree Acacia nigrescens when grown in different $ CO_{2} $ concentrations 2009 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract The photosynthetic responses of the tropical tree species Acacia nigrescens Oliv. grown at different atmospheric $ CO_{2} $ concentrations—from sub-ambient to super-ambient—have been studied. Light-saturated rates of net photosynthesis (Asat) in A. nigrescens, measured after 120 days exposure, increased significantly from sub-ambient (196 μL $ L^{−1} $) to current ambient (386 μL $ L^{−1} $) $ CO_{2} $ growth conditions but did not increase any further as [$ CO_{2} $] became super-ambient (597 μL $ L^{−1} $). Examination of photosynthetic $ CO_{2} $ response curves, leaf nitrogen content, and leaf thickness showed that this acclimation was most likely caused by reduction in Rubisco activity and a shift towards ribulose-1,5-bisphosphate regeneration-limited photosynthesis, but not a consequence of changes in mesophyll conductance. Also, measurements of the maximum efficiency of PSII and the carotenoid to chlorophyll ratio of leaves indicated that it was unlikely that the pattern of Asat seen was a consequence of growth [$ CO_{2} $] induced stress. Many of the photosynthetic responses examined were not linear with respect to the concentration of $ CO_{2} $ but could be explained by current models of photosynthesis. Elevated CO (dpeaa)DE-He213 Nitrogen content (dpeaa)DE-He213 Photosynthesis (dpeaa)DE-He213 Sub-ambient CO (dpeaa)DE-He213 Water-use efficiency (dpeaa)DE-He213 Nicholas Hewitt, C. verfasserin aut Enthalten in Planta Berlin : Springer, 1925 229(2009), 4 vom: 04. Jan., Seite 837-846 (DE-627)254639100 (DE-600)1463030-8 1432-2048 nnns volume:229 year:2009 number:4 day:04 month:01 pages:837-846 https://dx.doi.org/10.1007/s00425-008-0883-1 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_65 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_374 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_2018 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_2946 GBV_ILN_2949 GBV_ILN_2951 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 42.38 ASE AR 229 2009 4 04 01 837-846 |
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Enthalten in Planta 229(2009), 4 vom: 04. Jan., Seite 837-846 volume:229 year:2009 number:4 day:04 month:01 pages:837-846 |
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Possell, Malcolm @@aut@@ Nicholas Hewitt, C. @@aut@@ |
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Light-saturated rates of net photosynthesis (Asat) in A. nigrescens, measured after 120 days exposure, increased significantly from sub-ambient (196 μL $ L^{−1} $) to current ambient (386 μL $ L^{−1} $) $ CO_{2} $ growth conditions but did not increase any further as [$ CO_{2} $] became super-ambient (597 μL $ L^{−1} $). Examination of photosynthetic $ CO_{2} $ response curves, leaf nitrogen content, and leaf thickness showed that this acclimation was most likely caused by reduction in Rubisco activity and a shift towards ribulose-1,5-bisphosphate regeneration-limited photosynthesis, but not a consequence of changes in mesophyll conductance. Also, measurements of the maximum efficiency of PSII and the carotenoid to chlorophyll ratio of leaves indicated that it was unlikely that the pattern of Asat seen was a consequence of growth [$ CO_{2} $] induced stress. 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Possell, Malcolm |
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Possell, Malcolm ddc 580 bkl 42.38 misc Elevated CO misc Nitrogen content misc Photosynthesis misc Sub-ambient CO misc Water-use efficiency Gas exchange and photosynthetic performance of the tropical tree Acacia nigrescens when grown in different $ CO_{2} $ concentrations |
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580 ASE 42.38 bkl Gas exchange and photosynthetic performance of the tropical tree Acacia nigrescens when grown in different $ CO_{2} $ concentrations Elevated CO (dpeaa)DE-He213 Nitrogen content (dpeaa)DE-He213 Photosynthesis (dpeaa)DE-He213 Sub-ambient CO (dpeaa)DE-He213 Water-use efficiency (dpeaa)DE-He213 |
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gas exchange and photosynthetic performance of the tropical tree acacia nigrescens when grown in different $ co_{2} $ concentrations |
| title_auth |
Gas exchange and photosynthetic performance of the tropical tree Acacia nigrescens when grown in different $ CO_{2} $ concentrations |
| abstract |
Abstract The photosynthetic responses of the tropical tree species Acacia nigrescens Oliv. grown at different atmospheric $ CO_{2} $ concentrations—from sub-ambient to super-ambient—have been studied. Light-saturated rates of net photosynthesis (Asat) in A. nigrescens, measured after 120 days exposure, increased significantly from sub-ambient (196 μL $ L^{−1} $) to current ambient (386 μL $ L^{−1} $) $ CO_{2} $ growth conditions but did not increase any further as [$ CO_{2} $] became super-ambient (597 μL $ L^{−1} $). Examination of photosynthetic $ CO_{2} $ response curves, leaf nitrogen content, and leaf thickness showed that this acclimation was most likely caused by reduction in Rubisco activity and a shift towards ribulose-1,5-bisphosphate regeneration-limited photosynthesis, but not a consequence of changes in mesophyll conductance. Also, measurements of the maximum efficiency of PSII and the carotenoid to chlorophyll ratio of leaves indicated that it was unlikely that the pattern of Asat seen was a consequence of growth [$ CO_{2} $] induced stress. Many of the photosynthetic responses examined were not linear with respect to the concentration of $ CO_{2} $ but could be explained by current models of photosynthesis. |
| abstractGer |
Abstract The photosynthetic responses of the tropical tree species Acacia nigrescens Oliv. grown at different atmospheric $ CO_{2} $ concentrations—from sub-ambient to super-ambient—have been studied. Light-saturated rates of net photosynthesis (Asat) in A. nigrescens, measured after 120 days exposure, increased significantly from sub-ambient (196 μL $ L^{−1} $) to current ambient (386 μL $ L^{−1} $) $ CO_{2} $ growth conditions but did not increase any further as [$ CO_{2} $] became super-ambient (597 μL $ L^{−1} $). Examination of photosynthetic $ CO_{2} $ response curves, leaf nitrogen content, and leaf thickness showed that this acclimation was most likely caused by reduction in Rubisco activity and a shift towards ribulose-1,5-bisphosphate regeneration-limited photosynthesis, but not a consequence of changes in mesophyll conductance. Also, measurements of the maximum efficiency of PSII and the carotenoid to chlorophyll ratio of leaves indicated that it was unlikely that the pattern of Asat seen was a consequence of growth [$ CO_{2} $] induced stress. Many of the photosynthetic responses examined were not linear with respect to the concentration of $ CO_{2} $ but could be explained by current models of photosynthesis. |
| abstract_unstemmed |
Abstract The photosynthetic responses of the tropical tree species Acacia nigrescens Oliv. grown at different atmospheric $ CO_{2} $ concentrations—from sub-ambient to super-ambient—have been studied. Light-saturated rates of net photosynthesis (Asat) in A. nigrescens, measured after 120 days exposure, increased significantly from sub-ambient (196 μL $ L^{−1} $) to current ambient (386 μL $ L^{−1} $) $ CO_{2} $ growth conditions but did not increase any further as [$ CO_{2} $] became super-ambient (597 μL $ L^{−1} $). Examination of photosynthetic $ CO_{2} $ response curves, leaf nitrogen content, and leaf thickness showed that this acclimation was most likely caused by reduction in Rubisco activity and a shift towards ribulose-1,5-bisphosphate regeneration-limited photosynthesis, but not a consequence of changes in mesophyll conductance. Also, measurements of the maximum efficiency of PSII and the carotenoid to chlorophyll ratio of leaves indicated that it was unlikely that the pattern of Asat seen was a consequence of growth [$ CO_{2} $] induced stress. Many of the photosynthetic responses examined were not linear with respect to the concentration of $ CO_{2} $ but could be explained by current models of photosynthesis. |
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Gas exchange and photosynthetic performance of the tropical tree Acacia nigrescens when grown in different $ CO_{2} $ concentrations |
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| score |
7.3994255 |