Graduation date: 1994

Graduation date: 1993

The role of light and temperature on flowering of South African Watsonia species were evaluated to assess the potential for this genus as a commercial flower crop. Species were selected that represent different climatic regions of South Africa, with the aim of understanding how ecologically distinct species perform under cultivation. The four selected species were W. borbonica and W. tabularis (winter-rainfall area), W. angusta (shared rainfall) and W. pillansii (summer-rainfall area). In order to establish the optimum temperature required for flowering, plants were exposed for 12 weeks to three temperature regimes (12/7 °C, 21/15 °C and 29/21 °C) after attaining their first and/or second leaves. A temperature shift of 12/7 °C was used to assess if the plants had a vemalisation requirement. Controls were maintained under 25 % shade under natural conditions, with an average temperature of 24/7 °C. An elevated temperature of 29/21 °C was detrimental to plant growth. Moderate temperatures of 21/15 °C significantly (P<0.001) increased the height and the number of leaves produced per plant relative to the 12/7 °C treatment. These temperatures significantly (P<0.001) increased the total number of flowers produced per plant compared to low temperatures. However, flowering percentage and quality of flowers were reduced. A low temperature regime of 12/7 °C was efficient in satisfying vernalisation requirements and inducing flowering in four selected species. However, the total number of leaves produced per plant was signifcantly reduced. The summer-rainfall species, W pillansii, displayed a qualitative response to vernalisation, as no flowering was observed in non-vernalised plants. Two winter-rainfall species, W borbonica and W. tabularis, demonstrated a quantitative response to vernalisation. These species flowered at non-vernalising temperatures. W angusta behaved like the winter-rainfall species in terms of flowering. Overall, a vernalisaton treatment marginally reduced days to flower while flowering percentage was increased compared to other temperature regimes. However, there was no increase in the total number of flowers produced per plant. Low temperatures were not only effective for flower induction, but also for releasing corm dormancy, thus synchronising growth. Storing corms at either 4 or 10 QC resulted in 100 % sprouting within 4-6 weeks. The role of daylength in flowering of Watsonia plants was established by subjecting plants to long days (LO) of 16 h light and 8 h dark and to short days (SO) of 8 h light and 16 h dark. The number of leaves and flowering were significantly (P<0.01) promoted under the LO regime. However, there was strong temperature and daylength interaction in terms of flowering potential, as at low temperatures flowering was induced irrespective of daylength. In W. pillansii, flowering was obtained under both regimes (LO and SO) applied at the second leaf stage. Flowering in W. borbonica and W. tabularis was only observed under the LO regime at the second leaf stage. In both species, flowering was also obtained in SD-treated plants, provided treatment occurred after the formation of the third leaf. However, the total number and quality of flowers were reduced. To examine the effect of light intensity on flowering, plants at different developmental stages (first and/or second or beyond the third leaf stage) were exposed to photosynthetically active radiation (PAR) of 150 jJmol m-2s-1 or 39.5 jJmol m-2s-1 for 7 weeks. Exposure to low light intensity at either developmental stage compromised leaf quality. No flowering was observed following low light intensity treatment during the first to third leaf stages, even though plants were exposed to low temperature and LO regimes, both of which promoted flowering. Observation of the shoot apical meristem revealed that the second leaf stage was critical as the anatomical transition to flowering occurred at this level. When beyond the third leaf stage, low light intensity did not prevent flowering. However, the number of flowers produced per plant was reduced compared to plants maintained at 150 jJmol m-2s-1. Thus, light intensity played a role in both plant morphogenesis and flowering. LDs were effective in promoting vegetative growth whereas high light intensity and low temperature regimes played pivotal roles in flower induction. This makes them useful horticulture tools to produce desirable Watsonia plants for commercialisation. / Thesis (M.Sc.)-University of KwaZulu-Natal, Pietermaritzburg, 2006.

Indiana University-Purdue University Indianapolis (IUPUI) / The phototropin photoreceptors are important regulators of plant growth and development and can therefore affect the photosynthetic activity of plants. Phototropin1 and Phototropin2 are versatile protein kinases that become activated when exposed to blue light. Their photobiological actions are best understood in the model plant Arabidopsis thaliana, where they are known to trigger several responses to blue light, one of which is phototropism, the bending of plant organs towards light. Additionally, phot1 and phot2 drive stomatal opening, chloroplast arrangement in leaf cells, leaf expansion, and leaf orientation. The phot1-specific response is rapid inhibition of hypocotyl growth, leaf positioning and mRNA stability whereas phot2 mediates the chloroplast avoidance response to high light. These responses impact a plant’s ability to capture light for photosynthesis, therefore the phototropins play important roles in optimizing a plant’s photosynthetic activity. Soybean (Glycine max) is a very important crop plant in Indiana known for its nutritional versatility and is also utilized for biodiesel production.In spite of soybean being a key crop, there is currently no information about the functionality of soybean phototropins. Also, being a legume, soybean has many structural and functional features that are not present in Arabidopsis. Interestingly, PsPHOT1A (a photoreceptor from garden pea) was found to be a functional phototropin as it was able to complement the phot1 mutation in Arabidopsis. The roles of these proteins in soybean will be elucidated based on the hypothesis that soybean phototropins play essential roles in regulating photosynthetic activity as do the Arabidopsis phototropins. To date, five soybean phototropins, 3 PHOT1s and 2 PHOT2s, are believed to exist. These GmPHOT protein coding regions were amplified by RT-PCR and cloned into pCR8/TOPO or pENTR-D/TOPO vectors via TOPO cloning to utilize Gateway cloning technology to create plant transformation constructs subsequently. The cloned GmPHOT cDNAs from each of the 5 GmPHOTs were sequenced and compared to the GmPHOT sequences from the Phytozome database to assess the accuracy of the gene models. The gene models of all the GmPHOTs were found to be accurate except that of GmPHOT1B-2. The high level of sequence identity between the GmPHOTs and AtPHOTs and the conservation of LOV domains and catalytic domains indicate structural resemblance between them. This suggests that soybean phototropins should encode active photoreceptors. The cloned protein coding regions from soybean were then recombined into a plant expression vector via Gateway technology,which were then used for transformation of Agrobacterium tumefaciens. These plant expression constructs will be utilized in the future to determine the functionality of soybean phototropins in Arabidopsis.