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Xuan Wu, Shuyin Liang, and David H. Byrne

interaction of morphological traits in a tetraploid rose population BioMed Central Genet. 15 146 159 Godin, C. Costes, E. Sinoquet, H. 1999 A method for describing plant architecture which integrates topology and geometry Ann. Bot. 84 343 357 Green Industry

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C. Michael Bourget

than the LED's specified value and can potentially damage or destroy the LED. A circuit called a driver is used to regulate the current flowing through LEDs. There are many different driver designs and topologies available. The driver is the interface

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Thomas E. Marler, Vivian Lee, and Christopher A. Shaw

. 8 446 452 Cantatore, J.L. Murphy, S.M. Lynch, D.V. 2000 Compartmentation and topology of glucosylceramide synthesis Biochem. Soc. Trans. 28 748 750 Dehgan, B. Schutzman, B

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Arthur Villordon, Julio Solis, Don LaBonte, and Christopher Clark

was also classified into two distinct phenological stages: SR1 (1 to 10 DAT) and SR2 (10 to 20 DAT) ( Villordon et al., 2009a ). Where present, SR1 and SR2 were treated as “latent nodes” or “hidden variables.” The network structures or topologies of

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Rachel S. Leisso, Ines Hanrahan, James P. Mattheis, and David R. Rudell

analysis and “relative-betweenness centrality” for pathway topology analysis. Results and Discussion Values for harvest maturity indices were as follows: starch index (1–6) = 5.7 ± 0.072 ( se ), soluble solids = 12.9 ± 0.10 °Brix, titratable acidity = 0

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Antar Nasr El-Banna, Mohammed Elsayed El-Mahrouk, Mohammed Eraky El-Denary, Yaser Hassan Dewir, and Yougasphree Naidoo

accessions varied from 0.00% to 11.0%. The highest similarity value (11%) was between accession nos. 8 and 11. A dendrogram constructed by UPGMA cluster analysis using RAPD-based genetic distance is presented in Fig. 2 . The overall tree topology suggested a

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Karen Mitchell, Elizabeth French, Janna Beckerman, Anjali Iyer-Pascuzzi, Jeff Volenec, and Kevin Gibson

. However, this conclusion was based on a small number of studies ( n = 10) ( Biederman and Harpole, 2013 ), and the effect of biochar on RSA, which is the spatial arrangement or topology of plant roots, has been examined in only a few studies ( Abiven et

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Deborah Pagliaccia, Georgios Vidalakis, Greg W. Douhan, Ramiro Lobo, and Gary Tanizaki

genetic distances the mean character difference option and unweighted pair-group method with arithmetic averaging (UPGMA) were conducted using PAUP* (Version 4.0 beta 10) ( Swofford, 2002 ). Confidence in tree topology was examined using non

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Kalpana Sharma, Erica Goss, and Ariena H.C. van Bruggen

with both subtree pruning and regrafting and nearest neighbor interchange (NNI) topology searches. The size of the final alignment was 502 bp. Based on the phylogenetic relationships in Cannon et al. (2012) , C. dracaenophilum was included as an

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Jennifer A. Kimball, M. Carolina Zuleta, Matthew C. Martin, Kevin E. Kenworthy, Ambika Chandra, and Susana R. Milla-Lewis

and the dendrograms in NTSYSpc Version 2.2. To assess the robustness of the cluster analyses, topologies generated by UPGMA and NJ were compared and bootstrapping was performed ( Felsenstein, 1985 ) with 1000 replications using the Phylogenetic