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Studies on asparagus growth in relation to yield were undertaken in environmentally controlled growth cabinets and in greenhouses. Bud production during the annual growth cycle was also investigated in the field. Growth cabinet experiments showed that increasing the temperature had a significant effect on bud break and relative spear growth rate (RSGR), but although prior chilling had a significant effect on the length of time to bud break at 10°C and 15°C, the effect on RSGR was not so clear. The cytokinin-active compound, N-(2-chloro-4-pyridyl)-N'-phenylurea (CPPU), and the naturally occurring cytokinin, zeatin riboside (ZR) significantly stimulated spear elongation. However, spear leaf scale removal reduced spear elongation in the absence and presence of CPPU. CPPU only stimulated spear growth when spear leaf scales were present, indicating that other plant hormones may interact with cytokinins in promoting elongation. The importance of spear growth rate to yield was discussed. In greenhouse experiments, CPPU applied as a foliar spray at 10 or 20 mg L-1 was effective in producing longer and thicker cladodes that might be associated with increased photosynthetic rate. However, photosynthetic rate was unaffected by 10 mg L-1 CPPU treatment. Repeated CPPU applications to foliage reduced net assimilation rate (NAR) compared to untreated controls as determined by growth analysis studies. In asparagus plants, it was difficult to collect xylem sap and further experiments were undertaken with Capsicum annuum. The root exudate of CPPU-treated plants significantly decreased hypocotyl length in the lettuce gibberellin bioassay, suggesting that CPPU blocks gibberellin biosynthesis in roots. However, the application of GA3 to shoots did not reverse growth suppression caused by CPPU-treated roots. Bud production, both in growth cabinets and in open field plantings, started to occur during the spear harvest period in contrast to previously accepted views. During harvest three to four additional buds per cluster were produced in cabinet-grown plants and an average of 51 buds per m2 in field plantings. These results confirm that new bud initiation and development starts to occur during spear harvest, as well as during fern growth and establishment.

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Development of sustainable practices is an important goal in agriculture. One possibility involves the development of perennial cereal crops, but the mechanisms of perenniality first need to be understood. While in annual cereals flowering structures die following seed production, in perennial grasses, perenniality is achieved by maintaining at least one shoot in a vegetative state. There are two views on perennating tiller origin in perennial grasses: some authors suggest that all over-wintering tillers flower in spring and summer, leaving spring-initiated tillers to perennate, while others indicate that spring-initiated tillers are too immature to survive summer conditions, thereby implying that flowering must be prevented in some over-wintering tillers. An understanding of perenniality will therefore require an understanding of flowering control in these species. Temperate perennial grasses have dual induction requirements for flowering, where plants become competent to perceive inductive signals following vernalisation, and flowering is initiated by inductive photoperiods. Two hypotheses were formulated to test these models. The ‘environmental control hypothesis’ stated that all adequately vernalised perennial ryegrass tillers would flower on sufficient exposure to inductive photoperiods. Alternatively, the ‘spatial control hypothesis’ stated that in addition to the environmental mechanisms, a spatial control mechanism acts to regulate flowering. Two experiments were conducted to test these hypotheses. Perennial ryegrass and Italian (annual) ryegrass were induced to flower and differences between the annual and perennial habits at flowering time were observed. However neither hypothesis was proven. In the second experiment, flowering was studied in detail in individual tillers of perennial ryegrass. The eldest tiller flowered in all flowering plants. The second eldest tiller did not flower in 72% of plants with more than one reproductive tiller, while the third eldest tiller flowered in 94% of these plants. These data favour the spatial control hypothesis which suggests that a spatial regulatory mechanism might act to repress flowering in some competent perennial ryegrass tillers. These results were supported by studies of meristem morphology and by a preliminary gene expression study. Maintenance of older, established tillers in a vegetative state might allow the perennial plant a greater chance of survival during summer.

For millennia, scions have been grafted onto dwarfing apple rootstocks to reduce final tree size. However, it is unclear how scion architecture is first modified by the dwarfing apple rootstock, the time from grafting when this occurs and the endogenous hormonal signalling mechanisms that may cause the initial modifications in growth that then define the future architecture of the scion. In this study, the dwarfing (M.9) rootstock significantly decreased the mean total shoot length and node number of ‘Royal Gala’ apple scions by the end of the first year of growth from grafting when compared with rootstock(s) of greater vigour (MM.106, M.793 and a ‘Royal Gala’ rootstock control). Similarly, the auxin transport inhibitor 1-N-naphthylphthalamic acid (NPA) applied to the stem of vigorous rootstocks significantly decreased mean total shoot length and node number of the scion, and the architectural changes imposed were generally similar to those imposed by M.9. For example, both treatments decreased the mean length and node number of the primary shoot, reduced the formation of secondary axes on the primary shoot and caused a greater proportion of primary and secondary shoots (if present) to terminate growth early. Decreased formation of secondary axes imposed by both treatments was reversed by applying the cytokinin benzylaminopurine (BAP) repeatedly to the scion, whilst applications of gibberellins (GA4+7) reduced the proportion of primary and secondary shoots that terminated growth early, therefore increasing the final mean length and node number of these shoot types. Both M.9 and NPA also significantly decreased the final mean dry mass and length of the root system. Given these general similarities, it is proposed that the basipetal IAA signal is of central importance in rootstock-induced scion dwarfing, and that a shoot/root/shoot signalling mechanism may exist whereby the stem tissue of the M.9 rootstock decreases the basipetal transport of IAA to the root during summer, thereby decreasing root growth and the amount of rootproduced cytokinin and gibberellin transported to scion. Reduced amounts of cytokinin transported to the scion may decrease branching, whilst reduced amounts of gibberellins may decrease the duration for which a large proportion of primary and secondary shoots grow. Analysis of endogenous hormones for newly grafted composite ‘Royal Gala’ apple trees on rootstocks of different vigour provided some additional support for these ideas. It is recommended that future studies elucidate what unique properties of the M.9 bark act to restrict IAA transport, whilst it is concluded that gene(s) regulating rootstock-induced scion dwarfing are likely to control processes within the rootstock that modify the metabolism of IAA, its basipetal transport and the subsequent synthesis of root-produced vigour-inducing hormones including cytokinins and gibberellins.

Willow and poplar are the main trees used for soil erosion control in New Zealand (NZ) with successful establishment critical to greater use of this technology. Five experiments were conducted at the Pasture and Crop Research Unit, Massey University Palmerston North, NZ to examine the ability of willow and poplar to establish as a willow/poplar pasture system in NZ over a period of 3 years from December 2002 to April 2005. With an objective to select the best size for low cost planting, stem diameters (10 mm, 25 mm and 35 mm) were planted vertically and stem lengths (50 mm, 200 mm and 600 mm) were planted horizontally to determine their growth, establishment, biomass production and regrowth after browsing. From December 2002 to March 2003, three management treatments, mowing, herbicide and control (no weed control) treatments, were designed and applied to determine their effects on growth and shoot biomass production. From September 2004 to April 2005, mowing was replaced by sheep browsing and the effect of browsing, herbicide and control treatments on soil and tree water status (soil water content, soil water loss and deficit, and stem water potential) were examined. Longer (600 mm) and thicker stem diameters (35 mm) produced the greatest shoot biomass (edible biomass, total biomass and root biomass) compared to the thin stem cuttings (50 mm length and 10 mm diameter). Higher tree survival was also found for longer (600 mm) and thicker stems diameter (35 mm). The mown treatment produced significantly more edible and total shoot dry matter (DM) than the herbicide and control treatments, with willow clone 'Kinuyanagi' producing higher total shoot DM than 'Tangoio'. Pasture management had no significant effect on soil water content during spring 2004 and late summer/autumn 2005, however, it was significant during early and mid summer. Strong relationships between (i) soil water content and stem water potential (SWP), and (ii) SWP and soil water deficit were found and could help growers to predict the amount of water required during the growing season. The results clearly demonstrated that sheep grazing had negligible damaging effect on willow and poplar (main stem, branch breakage and tree leaning) and tree mortality, and that young trees can be browsed during pasture shortages in summer drought. Cutting size and understorey control for establishing willow and poplar into pasture have been better defined by this research. It is recommended that farmers establishing willow and poplar for fodder plant thick (vertical planting) and long stems (horizontal planting) for higher growth and biomass production.