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Brandon M. Miller and William R. Graves

caliper) were affected by the main effect of species, whereas only root dry weight was affected by treatment ( Table 1 ). Table 1. Significance of species and treatment main effects and their interactions on six responses to pruning and auxin treatments

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Yasutaka Kano

, sucrose accumulation has been demonstrated to occur in response to cellular enlargement if cell size is increased by auxin treatment during early fruit development ( Kano, 2002 ) as well as in response to heating fruits ( Kano, 2006 ). Conversely, sucrose

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Choun-Sea Lin, Krishnan Kalpana, Wei-Chin Chang, and Na-Sheng Lin

. The auxin treatments affected the morphology and length of the roots. NAA treatment resulted in more and longer roots relative to the other auxins ( Table 4 ). Although the lower concentration (9.05 μ m ) of 2,4-D, picloram, and dicamba increased

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Toshiki Asao, Hiroaki Kitazawa, Takuya Ban, M. Habibur Rahman Pramanik, and Kenzi Tokumasa

charcoal ( Asao et al., 1998 ; Kitazawa et al., 2005 ), degradation by microbial strains ( Asao et al., 2004a ), and auxin treatment ( Kitazawa et al., 2007 ) have been tested for the detoxification of exudates. Degradation of toxic compounds by electronic

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Cary J. Hebert, Darren H. Touchell, Thomas G. Ranney, and Anthony V. LeBude

number of segments producing shoots were recorded after 4 weeks. Each set of TDZ × auxin treatments was a separate experiment with a completely randomized factorial design (five rates of TDZ × five rates of auxin = 25 total plant growth regulator

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Khalid M. Elhindi, Yaser Hassan Dewir, Abdul-Wasea Asrar, Eslam Abdel-Salam, Ahmed Sharaf El-Din, and Mohamed Ali

increased the FGP for coriander from 27% to 52.3%. All other auxins treatments at different concentrations resulted in higher FGP than the control for the three plant species. IAA was more effective than IBA and NAA and showed stimulatory effects on seed

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Asma Alhussein Alawaadh, Yaser Hassan Dewir, Mona S. Alwihibi, Abdulhakim A. Aldubai, Salah El-Hendawy, and Yougasphree Naidoo

-auxin (≤0.5 mg·L −1 ) treatments yielded fewer, but longer, roots. Together, these results clearly demonstrate that exogenous auxin treatment is necessary to improve philodendron rooting. Previous studies have reported that the addition of NAA (0.5 mg·L −1

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Aliza Vardi, Ilan Levin, and Nir Carmi

( George et al., 1984 ; Talon et al., 1990 , 1992 ). In arabidopsis, GA 3 primarily influences mesocarp cell division, whereas mesocarp and exocarp cell enlargement occur after auxin treatment. In grape, GA 3 has been observed to induce cellular

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Mohamed S. Elmongy, Xiuyun Wang, Hong Zhou, and Yiping Xia

tested transcription was found to be upregulated by auxin treatments at different levels and at different time points. Our results suggest that transcription of IAA1 , IAA9 , IAA14 , and IAA27 genes may be considered a diagnostic marker for detecting

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Satoru Kondo, Hiroko Yamada, and Sutthiwal Setha

synthase in the ethylene pathway. For example, auxin treatment increased ACS2 messenger RNA (mRNA) levels in melons ( Cucumis me lo L.) ( Ishiki et al., 2000 ) and ACS3 and ACS5 mRNA levels in tomatoes ( Lycopersicon esculentum Mill.) ( Coenen et al