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Wenhao Dai and Cielo Castillo

medium containing 0.65% agar with four different auxin treatments (0, 0.1, 1, and 10 μ m NAA) under regular tissue culture conditions (described in “Plant Materials”). Rooting percentage and root number were recorded after 4 weeks of root development

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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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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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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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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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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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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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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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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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Michael T. Martin Jr., Geoffrey M. Weaver, Matthew R. Chappell, and Jerry Davis

of all nutrients in the leaves, upper, and lower stems remained constant over a 27-d propagation period; no nutrient mobility was observed. In a later study, nutrient movement was characterized in box-leaved holly cuttings with and without auxin