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Bermuda Capacity Principles in the Seventies, and Their Implication for JordanEl-Zoubi, Yousef Mohammad January 1977 (has links)
No description available.
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Grooming frequency and spacing effects on a TifEagle bermudagrass putting greenDunnivant, William Edwin, Guertal, Elizabeth A., January 2008 (has links) (PDF)
Thesis (M.S.)--Auburn University, 2008. / Abstract. Vita. Includes bibliographical references (p. 28-32).
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Bermudagrass dry matter yields as affected by nitrogen fertilizer, harvest frequency, clipping height and cultivarsSuwaysī, Muḥammad January 1981 (has links)
No description available.
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Mowing height, nitrogen rate and source effects on establishment and maintenance of Tifway and TifSport bermudagrassHicks, Christy Agnew, Guertal, Elizabeth A. January 2006 (has links) (PDF)
Thesis(M.S.)--Auburn University, 2006. / Abstract. Vita. Includes bibliographic references.
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CONTROL OF CYNODON DACTYLON WITH SETHOXYDIM AND FLUAZIFOP-BUTYL.de la Concha Duprat, Horacio A. January 1983 (has links)
No description available.
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Population dynamics and ecology of spiny lobsters Panulirus argus and P. guttatus at BermudaEvans, C. R. January 1989 (has links)
No description available.
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The evaluation of reserve carbohydrates in Midland Bermudagrass (Cynodon dactylon L.).Burris, Joseph Stephen, January 1965 (has links)
Thesis (M.S.)--Virginia Polytechnic Institute, 1966. / Typewritten. Vita. Abstract at end. Bibliography: leaves 30-32. Also available via the Internet.
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INFLUENCE OF NITROGEN, PHOSPHORUS, IRRIGATION, AND ROOT RESERVE LEVELS ON SEED YIELD COMPONENTS OF BERMUDAGRASSNascimento, Domicio do January 1978 (has links)
No description available.
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The pachytene and somatic chromosome morphology of Cynodon dactylon (L.) Pers.Brilman, Leah Ann Moore January 1978 (has links)
No description available.
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CHROMOSOME MORPHOLOGY IN CYNODON DACTYLON (L.) PERS.Brilman, Leah Ann Moore January 1981 (has links)
The pachytene bivalents of the tetraploid Cynodon dactylon var. dactylon could all be identified on the basis of characteristic morphological features including knobs, prominent chromomeres, chromosome length, long arm length, short arm length, arm ratio and relative length. The bivalents could be separated into two sets of chromosomes, D and D', with the D genome being homologous to that found in the diploids, C. dactylon vars. aridus and afghanicus. The two sets are homoeologous as shown by the occasional formation of quadrivalents and the closeness of chromosome measurements, although chromomere patterns and knobs differed. C. dactylon var. dactylon therefore appears to be a segmental allotetraploid. In prophase somatic spreads of var. dactylon two sets of chromosomes could also be separated by heterochromatic patterns. In both the diploids, vars. aridus and afghanicus, and the tetraploid the somatic chromosomes could be homologised with their corresponding pachytene bivalents. The chromosomes were of different relative lengths during the two phases. A polyhaploid obtained from a twin seedling of C. dactylon var. dactylon showed both univalents and bivalents in a diplotene spread, supporting a segmental allopolyploid origin of var. dactylon. This plant reverted back to a tetraploid state before further studies could be made. Giemsa C-banding, using barium hydroxide at room temperature for 50 minutes and 2xSSC at 60°C for 30 minutes to pretreat the slides before staining, produced telomeric bands in the position of the knobs seen in standard acetocarmine squash.
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