Change in pH regimes and adventitious root induction in semi-hardwood cuttings of Gmelina arborea Roxb.
Abstract Change in pH regimes (pH 5.5–8.5), IBA (0.5 mM) and their interactions significantly influenced adventitious root induction and growth in semi-hardwood shoot cuttings collected from annually hedged Gmelina arborea Roxb. stockplants of 4 years of age and maintained in earthen pots. Acidic pH...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Kumar, Pramod [verfasserIn] Jharia, Surendra Kumar [verfasserIn] Ansari, Shamim Akhtar [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2011 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Plant growth regulation - Dordrecht : Springer Science + Business Media B.V., 1982, 65(2011), 3 vom: 27. Juli, Seite 531-536 |
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| Übergeordnetes Werk: |
volume:65 ; year:2011 ; number:3 ; day:27 ; month:07 ; pages:531-536 |
| Links: |
|---|
| DOI / URN: |
10.1007/s10725-011-9617-7 |
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| Katalog-ID: |
SPR012761702 |
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| 520 | |a Abstract Change in pH regimes (pH 5.5–8.5), IBA (0.5 mM) and their interactions significantly influenced adventitious root induction and growth in semi-hardwood shoot cuttings collected from annually hedged Gmelina arborea Roxb. stockplants of 4 years of age and maintained in earthen pots. Acidic pH 5.5 administered for 4 h as 5.0 mM potassium phosphate buffer significantly promoted rooting ability (%) and root number $ cutting^{−1} $ and was the second best for root biomass after neutral pH 7.0. The effectiveness for induction and growth of adventitious roots was as follows: pH 5.5 > pH 8.5 > pH 7.0. Addition of IBA was ineffective at pH 5.5–7.0 and inhibitory at pH 8.5 for induction and growth of adventitious roots. The findings suggest a direct role of acidic pH, independent of auxin, in the process of adventitious root formation, encouraging in depth investigation for detection and characterization of pH dependent expression of early transcriptomes and their association with functioning of auxin signal transduction system in the process. | ||
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| 650 | 4 | |a Cellular competence |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Clonal propagation |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a pH |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Indole 3-butyric acid (IBA) |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a White teak |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Jharia, Surendra Kumar |e verfasserin |4 aut | |
| 700 | 1 | |a Ansari, Shamim Akhtar |e verfasserin |4 aut | |
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10.1007/s10725-011-9617-7 doi (DE-627)SPR012761702 (SPR)s10725-011-9617-7-e DE-627 ger DE-627 rakwb eng 333.7 580 ASE 48.50 bkl 42.41 bkl 48.52 bkl Kumar, Pramod verfasserin aut Change in pH regimes and adventitious root induction in semi-hardwood cuttings of Gmelina arborea Roxb. 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Change in pH regimes (pH 5.5–8.5), IBA (0.5 mM) and their interactions significantly influenced adventitious root induction and growth in semi-hardwood shoot cuttings collected from annually hedged Gmelina arborea Roxb. stockplants of 4 years of age and maintained in earthen pots. Acidic pH 5.5 administered for 4 h as 5.0 mM potassium phosphate buffer significantly promoted rooting ability (%) and root number $ cutting^{−1} $ and was the second best for root biomass after neutral pH 7.0. The effectiveness for induction and growth of adventitious roots was as follows: pH 5.5 > pH 8.5 > pH 7.0. Addition of IBA was ineffective at pH 5.5–7.0 and inhibitory at pH 8.5 for induction and growth of adventitious roots. The findings suggest a direct role of acidic pH, independent of auxin, in the process of adventitious root formation, encouraging in depth investigation for detection and characterization of pH dependent expression of early transcriptomes and their association with functioning of auxin signal transduction system in the process. Adventitious rooting (dpeaa)DE-He213 Beechwood (dpeaa)DE-He213 Cellular competence (dpeaa)DE-He213 Clonal propagation (dpeaa)DE-He213 pH (dpeaa)DE-He213 Indole 3-butyric acid (IBA) (dpeaa)DE-He213 White teak (dpeaa)DE-He213 Jharia, Surendra Kumar verfasserin aut Ansari, Shamim Akhtar verfasserin aut Enthalten in Plant growth regulation Dordrecht : Springer Science + Business Media B.V., 1982 65(2011), 3 vom: 27. Juli, Seite 531-536 (DE-627)270932941 (DE-600)1478400-2 1573-5087 nnns volume:65 year:2011 number:3 day:27 month:07 pages:531-536 https://dx.doi.org/10.1007/s10725-011-9617-7 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_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 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_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 48.50 ASE 42.41 ASE 48.52 ASE AR 65 2011 3 27 07 531-536 |
| spelling |
10.1007/s10725-011-9617-7 doi (DE-627)SPR012761702 (SPR)s10725-011-9617-7-e DE-627 ger DE-627 rakwb eng 333.7 580 ASE 48.50 bkl 42.41 bkl 48.52 bkl Kumar, Pramod verfasserin aut Change in pH regimes and adventitious root induction in semi-hardwood cuttings of Gmelina arborea Roxb. 2011 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Change in pH regimes (pH 5.5–8.5), IBA (0.5 mM) and their interactions significantly influenced adventitious root induction and growth in semi-hardwood shoot cuttings collected from annually hedged Gmelina arborea Roxb. stockplants of 4 years of age and maintained in earthen pots. Acidic pH 5.5 administered for 4 h as 5.0 mM potassium phosphate buffer significantly promoted rooting ability (%) and root number $ cutting^{−1} $ and was the second best for root biomass after neutral pH 7.0. The effectiveness for induction and growth of adventitious roots was as follows: pH 5.5 > pH 8.5 > pH 7.0. Addition of IBA was ineffective at pH 5.5–7.0 and inhibitory at pH 8.5 for induction and growth of adventitious roots. The findings suggest a direct role of acidic pH, independent of auxin, in the process of adventitious root formation, encouraging in depth investigation for detection and characterization of pH dependent expression of early transcriptomes and their association with functioning of auxin signal transduction system in the process. Adventitious rooting (dpeaa)DE-He213 Beechwood (dpeaa)DE-He213 Cellular competence (dpeaa)DE-He213 Clonal propagation (dpeaa)DE-He213 pH (dpeaa)DE-He213 Indole 3-butyric acid (IBA) (dpeaa)DE-He213 White teak (dpeaa)DE-He213 Jharia, Surendra Kumar verfasserin aut Ansari, Shamim Akhtar verfasserin aut Enthalten in Plant growth regulation Dordrecht : Springer Science + Business Media B.V., 1982 65(2011), 3 vom: 27. Juli, Seite 531-536 (DE-627)270932941 (DE-600)1478400-2 1573-5087 nnns volume:65 year:2011 number:3 day:27 month:07 pages:531-536 https://dx.doi.org/10.1007/s10725-011-9617-7 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_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 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_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 48.50 ASE 42.41 ASE 48.52 ASE AR 65 2011 3 27 07 531-536 |
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Enthalten in Plant growth regulation 65(2011), 3 vom: 27. Juli, Seite 531-536 volume:65 year:2011 number:3 day:27 month:07 pages:531-536 |
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Adventitious rooting Beechwood Cellular competence Clonal propagation pH Indole 3-butyric acid (IBA) White teak |
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Kumar, Pramod @@aut@@ Jharia, Surendra Kumar @@aut@@ Ansari, Shamim Akhtar @@aut@@ |
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Kumar, Pramod |
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Kumar, Pramod ddc 333.7 bkl 48.50 bkl 42.41 bkl 48.52 misc Adventitious rooting misc Beechwood misc Cellular competence misc Clonal propagation misc pH misc Indole 3-butyric acid (IBA) misc White teak Change in pH regimes and adventitious root induction in semi-hardwood cuttings of Gmelina arborea Roxb. |
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333.7 580 ASE 48.50 bkl 42.41 bkl 48.52 bkl Change in pH regimes and adventitious root induction in semi-hardwood cuttings of Gmelina arborea Roxb Adventitious rooting (dpeaa)DE-He213 Beechwood (dpeaa)DE-He213 Cellular competence (dpeaa)DE-He213 Clonal propagation (dpeaa)DE-He213 pH (dpeaa)DE-He213 Indole 3-butyric acid (IBA) (dpeaa)DE-He213 White teak (dpeaa)DE-He213 |
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ddc 333.7 bkl 48.50 bkl 42.41 bkl 48.52 misc Adventitious rooting misc Beechwood misc Cellular competence misc Clonal propagation misc pH misc Indole 3-butyric acid (IBA) misc White teak |
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ddc 333.7 bkl 48.50 bkl 42.41 bkl 48.52 misc Adventitious rooting misc Beechwood misc Cellular competence misc Clonal propagation misc pH misc Indole 3-butyric acid (IBA) misc White teak |
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Change in pH regimes and adventitious root induction in semi-hardwood cuttings of Gmelina arborea Roxb. |
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Change in pH regimes and adventitious root induction in semi-hardwood cuttings of Gmelina arborea Roxb |
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change in ph regimes and adventitious root induction in semi-hardwood cuttings of gmelina arborea roxb |
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Change in pH regimes and adventitious root induction in semi-hardwood cuttings of Gmelina arborea Roxb. |
| abstract |
Abstract Change in pH regimes (pH 5.5–8.5), IBA (0.5 mM) and their interactions significantly influenced adventitious root induction and growth in semi-hardwood shoot cuttings collected from annually hedged Gmelina arborea Roxb. stockplants of 4 years of age and maintained in earthen pots. Acidic pH 5.5 administered for 4 h as 5.0 mM potassium phosphate buffer significantly promoted rooting ability (%) and root number $ cutting^{−1} $ and was the second best for root biomass after neutral pH 7.0. The effectiveness for induction and growth of adventitious roots was as follows: pH 5.5 > pH 8.5 > pH 7.0. Addition of IBA was ineffective at pH 5.5–7.0 and inhibitory at pH 8.5 for induction and growth of adventitious roots. The findings suggest a direct role of acidic pH, independent of auxin, in the process of adventitious root formation, encouraging in depth investigation for detection and characterization of pH dependent expression of early transcriptomes and their association with functioning of auxin signal transduction system in the process. |
| abstractGer |
Abstract Change in pH regimes (pH 5.5–8.5), IBA (0.5 mM) and their interactions significantly influenced adventitious root induction and growth in semi-hardwood shoot cuttings collected from annually hedged Gmelina arborea Roxb. stockplants of 4 years of age and maintained in earthen pots. Acidic pH 5.5 administered for 4 h as 5.0 mM potassium phosphate buffer significantly promoted rooting ability (%) and root number $ cutting^{−1} $ and was the second best for root biomass after neutral pH 7.0. The effectiveness for induction and growth of adventitious roots was as follows: pH 5.5 > pH 8.5 > pH 7.0. Addition of IBA was ineffective at pH 5.5–7.0 and inhibitory at pH 8.5 for induction and growth of adventitious roots. The findings suggest a direct role of acidic pH, independent of auxin, in the process of adventitious root formation, encouraging in depth investigation for detection and characterization of pH dependent expression of early transcriptomes and their association with functioning of auxin signal transduction system in the process. |
| abstract_unstemmed |
Abstract Change in pH regimes (pH 5.5–8.5), IBA (0.5 mM) and their interactions significantly influenced adventitious root induction and growth in semi-hardwood shoot cuttings collected from annually hedged Gmelina arborea Roxb. stockplants of 4 years of age and maintained in earthen pots. Acidic pH 5.5 administered for 4 h as 5.0 mM potassium phosphate buffer significantly promoted rooting ability (%) and root number $ cutting^{−1} $ and was the second best for root biomass after neutral pH 7.0. The effectiveness for induction and growth of adventitious roots was as follows: pH 5.5 > pH 8.5 > pH 7.0. Addition of IBA was ineffective at pH 5.5–7.0 and inhibitory at pH 8.5 for induction and growth of adventitious roots. The findings suggest a direct role of acidic pH, independent of auxin, in the process of adventitious root formation, encouraging in depth investigation for detection and characterization of pH dependent expression of early transcriptomes and their association with functioning of auxin signal transduction system in the process. |
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Change in pH regimes and adventitious root induction in semi-hardwood cuttings of Gmelina arborea Roxb. |
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| score |
7.4021244 |