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Junji Amano, Sachiko Kuwayama, Yoko Mizuta, Masaru Nakano, Toshinari Godo, and Hajime Okuno

the parental plants. After 2 years of cultivation, tubers of the hybrids were divided and transplanted to new pots as were the parental plants. Three years after cultivation of the hybrid plants in the greenhouse, morphological characterization

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Dario J. Chavez and Paul M. Lyrene

); and 4) tetraploid plants with both pollen tetrads and stomatal guard cell length large (4x–4x). Morphological studies of colchicine-derived plants Ten 2x–2x V. darrowii genotypes, one 4x–2x periclinal chimera, three 2x–4x periclinal chimeras

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Daljeet S. Dhaliwal and Martin M. Williams II

seed cost. The objectives of this study were to a) evaluate edamame plant morphology and yield response to plant density and b) determine the EOPD of machine-harvested edamame. Materials and Methods Germplasm selection and seed treatment. Edamame

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Martin M. Williams II

energy and driving photosynthesis, undergoes distinct morphological changes as planting date is delayed. The extent to which this information results in crop management improvements remains to be seen. Perhaps optimal level of certain crop management

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Jack E. Staub, Matthew D. Robbins, Yingmei Ma, and Paul G. Johnson

9025897. Because historical information about this population is limited, very little is known about the genetic or morphological characteristics of this plant material. Using five plants of FEID 9025897 in an AFLP-based analysis, Jones et al. (2008

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Brian Christensen, Sridevy Sriskandarajah, and Renate Müller

Union ( European Union, 2001 ). Furthermore, by using wild-type strains, no marker genes are needed for selection, because transformed plants can be selected based on the hairy root morphology ( Christensen et al., 2008 ; Giovannini et al., 1997

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Gyeong Ran Do, Ju Hee Rhee, Wan Soon Kim, Yun Im Kang, In Myung Choi, Jeom Hwa Han, Hyun Hee Han, Su Hyun Ryu, and Han Chan Lee

al., 2005 , 2006 ). The gross morphology of the diploid form with numerous stem-bulbils closely resembles that of the triploid form ( Kim et al., 2005 ; Noda, 1978 ). The fact that triploid plants have mostly sterile pollens is already widely known

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Kelly M. Oates, Darren H. Touchell, and Thomas G. Ranney

Institute Inc., Cary, NC). Evaluation of morphology, phenology, survival, and pollen viability. Plant height, number of flowers, diameter of flowers (six per plant), date of first anthesis, winter survival, pollen viability, number of stems, number of nodes

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Juran C. Goyali, Abir U. Igamberdiev, and Samir C. Debnath

unintended clonal variability. Several strategies have been used to assess the clonal fidelity of TC derived plants of several fruit species but with limited success ( Debnath, 2008 ). Phenotypic identification based on morphological traits is influenced by

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Hamidou F. Sakhanokho and M. Nurul Islam-Faridi

culture potential through shoot apex culture and somatic embryogenesis. Among the clonally propagated plants through shoot, apex of one the accessions (PI 636107) was a single plant that was morphologically different from all the rest. This particular