M. S.

The most important problem in using bermudagrass (Cynodon sp.) for turf at the northern limit of its adaptation is winter survival. Bermudagrass used for athletic complexes is exposed to the additional problem of uncontrolled or excessive traffic. This research was conducted to determine the effects of: 1) traffic and mineral nutrition; 2) clear plastic covers and cultural treatments and; 3) overseeding and late winter freezing on bermudagrass winter survival. Four separate experiments were conducted on field cultured Midiron bermudagrass. Various regimes of traffic, N and K fertility, clear plastic covers, cultural treatments and growth regulators were utilized to determine their affect on bermudagrass winter survival. A laboratory freeze was used, in two experiments, on plant samples taken from the field. Following the freezing procedure, the samples were then grown in the greenhouse. From these experiments, it was found that traffic applied just as turf growth initiates in the spring was the most damaging. Potassium fertility had no effect on post dormancy growth. Nitrogen did improve post dormancy growth of bermudagrass exposed to a late winter laboratory freeze and when plastic covers were applied during winter dormancy. Plastic covers enhanced post dormancy growth and offset the detrimental effect of imposed traffic. 'Stayz Green' turf colorant did increase early post dormancy growth. While, the cultivation treatments using a vertical mower alone and with an aerifier reduced early green up. Flurprimidal reduced early post dormancy growth of bermudagrass; while, mefluidide had no detrimental effect. Both growth regulators reduced the growth of the overseeded ryegrass, and mefluidide enhanced the competitiveness of bermudagrass in the ryegrass canopy. / M.S.

Bermudagrass (<i>Cynodon</i> spp.), when cultured at the northern limit of adaptation for semitropical grasses, is exposed seasonally to temperatures low enough to limit growth and turf quality. Research was conducted to investigate the influence of foliar iron and cytokinin applications on bermudagrass growth during fall and spring. The relationship of photosynthesis, respiration, and nonstructural carbohydrate composition to chilling temperatures was also studied. Foliar applications of Fe in late-summer and fall extended bermudagrass performance during low temperature periods of fall. Frequent Fe applications aided the retention of green bermudagrass turf during prolonged exposure to chilling temperatures. Iron applied the previous season stimulated post-dormancy recovery. Benzyladenine (BA) applied alone was not as effective as Fe for promoting green bermudagrass color retention during fall and BA had few effects on spring growth when applied the previous season. Applications of BA in conjunction with Fe were beneficial for retention of green bermudagrass color during late fall when clear plastic covers were used to prevent frost injury. A 6- to 8-week longer bermudagrass growing season occurred when clear plastic covers were used to prevent frost injury. Iron and BA did not significantly affect the total nonstructural carbohydrate (TNC) levels in Midiron bermudagrass rhizomes and stolons at the onset of dormancy in field studies. Midiron bermudagrass had higher photosynthetic and respiration rates than Tifgreen bermudagrass after 4 days exposure to chilling (10/7°C day/night) temperatures in controlled environment studies. Midiron recovered higher photosynthetic rates than Tifgreen when returned to a warm (30°C) environment after exposure to chilling temperatures. The TNC in leaves of Midiron and Tifgreen increased 88 and 160%, respectively, during 5 days at chilling temperatures. The inability to transport carbohydrate from and the subsequent accumulation of high photoassimilate levels in leaves was associated with the inability of bermudagrass to fully recover high photosynthetic rates following chilling. Reduced respiratory activity was apparently responsible for the accumulation of high TNC levels in leaves. In contrast to photosynthesis, respiration was reversibly inhibited by short term exposure of bermudagrass to chilling temperatures. Rapid recovery of high respiratory activity may be important for maintenance of aesthetically pleasing bermudagrass turf following chilling. Foliar applied Fe or BA generally caused darker green Midiron and Tifgreen turf after exposure to chilling temperatures in a controlled environment, although the enhancement of physiological activity differed with chemical applied and cultivar. Iron stimulated recovery of photosynthetic and respiratory activity in both cultivars after exposure to chilling temperatures. However, during chilling Midiron CO₂ exchange was more responsive to Fe applications. Benzyladenine increased photosynthesis in Tifgreen but not in Midiron and did not significantly affect respiration in either cultivar. Neither Fe nor BA had a consistent effect on TNC levels in bermudagrass leaves, rhizomes, or stolons. These investigations indicate that cultivar selection may play a major role in determining turf quality at chilling temperatures. Iron may modify bermudagrass physiology and enhance performance of bermudagrass exposed to chilling temperatures. / Ph. D. / incomplete_metadata

No description available.

Indiana University-Purdue University Indianapolis (IUPUI) / Drought and cold conditions are among the major factors affecting plant growth and crop production globally. Dehydrins are group II late embryogenesis abundant (LEA) proteins characterized by a conserved K-region (EKKGIMDKIKEKLPG consensus sequence) that accumulate in many plants during drought, low temperature, and high salinity to confer stress tolerance. While it has been demonstrated that overexpression of dehydrins improves cold tolerance in various crop plants, the mechanism leading to cold tolerance is still unclear. Previous studies reported phosphorylation of AtERD14 dehydrin by casein kinase II (CKII) led to an increase in calcium binding activity. Mass spectroscopy analysis determined that the phosphorylation was localized to a poly-serine (S) region. To further characterize the S-region, GST fused ERD14 mutants were created via site-directed mutagenesis and deletion of either the amino or carboxyl ends of ERD14 via the QuickChange® Multi Site-Directed Mutagenesis Kit. Phosphorylation of purified mutant proteins by CKII was analyzed via gel shift and direct phosphorylation assays. The effect of phosphorylation on calcium binding activity was also analyzed. Results showed the serine (S) residue at position 83 was crucial to phosphorylation-dependent molecular mass shift and Ca2+-binding activities followed by the serine residue at position 85 in importance. Mutation of serines at positions 83, 84, and 85 completely eliminated the phosphorylation-dependent gel shift and calcium binding. Examination of truncation mutants determined the N-terminal was an important region for protein structure modification and phosphorylation ability leading to Ca2+ activation. Calcium binding activity of the truncated mutants indicated the calcium binding site was localized in the region between the S-region and the K-region near the C-terminal end. To characterize the acidic dehydrins contribution to cold tolerance in vivo, three single (erd10, erd14, cor47) knockouts (KOs) were characterized. Single KOs produced no cold sensitive phenotype indicating the need for multiple dehydrin KOs in Arabidopsis in order to potentially produce a cold sensitive phenotype.

Indiana University-Purdue University Indianapolis (IUPUI) / Dehydrins are type II LEA proteins induced in many plants during drought, low temperature, and high salinity to confer stress tolerance. AtERD14 is an Arabidopsis thaliana dehydrin that functions in part of the cold stress pathway. AtERD14 has chaperone-like capabilities that allow it to bind and protect various proteins from dehydration stresses. In order to determine the necessary components for cold induction of AtERD14, AtERD14prom::GFP/GUS and AtERD14prom::AtERD14 in AtERD14 KO constructs were created and stably transformed into A. thaliana. Analysis of the constructs showed the AtERD14 promoter alone was insufficient to respond to cold, and it was necessary to attach the AtERD14 coding region to the promoter to induce a cold response in ERD14. On the other hand, the RD29aprom::GFP/GUS promoter did respond to cold stress, indicating that RD29a does not require its coding region to support an increased amount of reporter activity after cold stress. The protoplast transformation system, while capable of transient expression of introduced constructs in protoplasts, was difficult for use for cold-inducible expression.