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A field experiment was conducted to examine the responses in growth, total dry matter (TDM), seed yield and nitrogen (N) accumulation of Kabuli chickpea cv. Principe and narrow-leafed lupin cv. Fest to different irrigation levels and N fertilizer on a Templeton silt loam soil at Lincoln University, Canterbury, New Zealand in 2007/08. The irrigation and fertilizer treatments were double full irrigation, full irrigation, half irrigation and nil irrigation and a control, full irrigation plus 150 kg N ha⁻¹. There was a 51 % increase in the weighed mean absolute growth rate (WMAGR) by full irrigation over no irrigation. The maximum growth rates (MGR) followed a similar response. The growth rates were not significantly decreased by double irrigation. Further, N fertilizer did not significantly improve crop growth rates. With full irrigation MGRs were 27.6 and 34.1 g m⁻² day⁻¹ for Kabuli chickpea and narrow-leafed lupin, respectively. Seed yields of fully-irrigated crops were trebled over the nil irrigation treatment. With full irrigation, seed yield of chickpea was 326 and that of lupin was 581 g m⁻². Seed yield of the two legumes was reduced by 45 % with double irrigation compared with full irrigation. Nitrogen fertilizer did not increase seed yields in either legume. Increased seed yield with full irrigation was related to increased DM, and crop growth rates, seeds pod⁻¹ and seeds m⁻². Crop harvest index (CHI) was significantly (P < 0.05) increased by irrigation and was related to seed yield only in narrow-leafed lupin. With full irrigation, the crops intercepted more than 95 % of incoming incident radiation at leaf area indices (LAIs), 2.9 and 3 or greater in Kabuli chickpea and narrow-leafed lupin, respectively. In contrast, without irrigation the two legumes achieved a maximum fraction of radiation intercepted of less than 90 %. With full irrigation, total intercepted photosynthetically active radiation (PAR) was increased by 28 % and 33 % over no irrigation for Kabuli chickpea and narrow-leafed lupin, respectively. Fully-irrigated Kabuli chickpea intercepted a total amount of PAR of 807 MJ m⁻² and fully-irrigated narrow-leafed lupin intercepted 1,042 MJ m⁻². Accumulated DM was strongly related to accumulated intercepted PAR (R² ≥ 0.96**). The final RUE was significantly (P < 0.001) increased by irrigation. With full irrigation the final RUE of Kabuli chickpea was 1.49 g DM MJ⁻¹ PAR and that of narrow-leafed lupin was 2.17 g DM MJ⁻¹ PAR. Total N accumulation of Kabuli chickpea was not significantly affected by irrigation level. Kabuli chickpea total N was increased by 90 % by N fertilizer compared to fully-irrigated Kabuli chickpea which produced 17.7 g N m⁻². In contrast, total N accumulated in narrow-leafed lupin was not increased by N fertilizer but was decreased by 75 % with no irrigation and by 25 % with double irrigation (water logging) compared to full irrigation with a total N of 45.9 g m⁻². Total N was highly significantly related to TDM (R² = 0.78** for Kabuli chickpea and R² = 0.99** for narrow-leafed lupin). Nitrogen accumulation efficiency (NAE) of narrow-leafed lupin was not affected by irrigation or by N fertilizer. However, the NAE of Kabuli chickpea ranged from 0.013 (full irrigation) to 0.020 (no irrigation) and 0.017 g N g⁻¹ DM (full irrigation with N fertilizer). The N harvest index (NHI) was not affected by irrigation, N fertilizer or legume species. The NHI of Kabuli chickpea was 0.50 and that of narrow-leafed lupin was 0.51. The NHI was significantly (r ≥ 0.95 **) related to CHI.

This research examined the mechanisms by which temperature, water availability and nitrogen (N) affect the dry matter (DM) yield potential of cocksfoot (Dactylis glomerata L.) dominant pastures. The experiment was a split plot design with main plots of fully irrigated (I) or dryland (D), sub-plots of N fertiliser at 800 kg N/ha in 2003/04; and 1600 kg N/ha in 2004/05 (+N) or 0 kg N/ha (-N). The potential environmental yield of an established 8 year old cocksfoot dominant pasture was 21.9 t DM/ha/y from I+N pastures compared with 9.8 t DM/ha by I-N pastures and 15.1 t DM/ha/y by D+N pastures. The lowest yields were from dryland pastures with no N which produced 7.5 t DM/ha/y in 2003/03 and 5.0 t DM/ha/y in 2004/05. The effect of seasonal temperatures on the DM production, when periods of water stress were excluded, was quantified using thermal time accumulated above a base temperature of 3°C as 7.0 kg DM/°Cd/ha for N fertilised pastures and 3.3 kg DM/°Cd/ha for pastures with no N. The 2.5 t DM/ha difference in yields of D-N pastures in 2003/04 and 2004/05 was the result of the duration, extent and timing of the water stress period. In both years the critical limiting deficit (DL) was calculated as 78 mm from the soil moisture deficit in the 0-0.8 m soil layers. Beyond DL yield decreased at a rate of 1.45%/mm in +N and –N pastures, relative to fully irrigated control pastures. Yields of D+N and D-N pastures were similar during periods of water stress with 0.4±0.1 t/DM/ha produced during the rotation ending 30/12/2003. This was less than from either the I-N (1.2 t DM/ha) or I+N (3.5 t DM/ha) pastures due to the reduction in the amount of photosynthetically active radiation intercepted by the canopies of the dryland pastures. However, in the rotation ending 2/5/2004, after autumn rain alleviated drought conditions, yield of the D+N pasture was 2.1 t DM/ha compared with 1.7 t DM/ha by I+N pastures. The effect of N on yield was described using a nutrition index which showed that as DM yield increased N% in the herbage declined. This is a function of the ratio between metabolic and structural N requirements rather than caused by ontogeny alone. Specific leaf N was determined at two harvests and appeared constant at a given point in time (1.0-1.6 g N/m² leaf). In contrast, specific pseudostem N increased from 0.8-1.0 g N/m² pseudostem at an NNI of 0.4 in –N pastures to 2.6-3.0 g N/m² pseudostem at an NNI of 1.2 in the +N pastures. Differences between the yields of +N and –N pastures were caused by differences in radiation use efficiency (RUE) as determined by the linear relationship (R²=0.76) between RUE and the nitrogen nutrition index (NNI). In this thesis, empirical relationships for the effects of temperature, water availability and N were derived and the physiological mechanisms which underlie these descriptions were identified. These relationships provide clear and simple explanations of the effects of environmental variables on the productivity of cocksfoot based pastures which will enhance understanding of the benefits and limitations of cocksfoot, particularly in dryland farming systems.

Genotypic differences in growth and yield of two common bean (Phaseolus vulgaris L) cultivars to Rhizobium inoculation and management were investigated. In 2003-04, the two bean cultivars (Scylla and T-49) were combined with three inoculant treatments (strains CC 511 and RCR 3644, and a control of no inoculation), two fertiliser levels (0 and 150 kg N ha⁻¹) and two irrigation treatments (irrigated and rainfed). There was no nodulation on either cultivar. To further investigate the symbiotic relationship, 16 rhizobial isolates, including the two used in the first field experiment, were combined with the cultivar Scylla and evaluated in a greenhouse. Subsequently, five Rhizobium isolates were chosen for further field evaluation, based on signs of early nodulation in the greenhouse trial. The second field experiment in 2004-05 combined the five inoculant strains (RCR 3644, UK 2, H 20, PRF 81, PhP 17 and a control) with two bean cultivars (Scylla and T-49). In the greenhouse, nodule number varied from 7 (UK 2) to 347 (H 441) nodules plant⁻¹ at 51 DAS and from 13 (UK 1) to 335 (CIAT 899) nodules plant⁻¹ at 85 DAS. In 2004-05, in the field, nodulation was also variable, ranging between 1 and approximately 70 nodules plant⁻¹, with higher nodules numbers plant⁻¹ being found on cultivar T-49. Of the isolates used in the field, strains H 20, PRF 81 and PhP 17 produced 70, 25 and 12 nodules plant⁻¹ at 70, 40 and 54 DAS respectively. Nodules formed were of various sizes and more than 80 % were pink to dark red in colour denoting the presence of leghaemoglobin and active N fixation. The remaining nodules were either green or white. The importance of selecting an appropriate cultivar for the growing conditions was highlighted in these experiments. Leaf area index, leaf area duration intercepted radiation and final utilisation efficiency were significantly affected by cultivar. In both seasons cv. T-49 reached maturity (dry seed) before Scylla, while unirrigated plants reached green pod maturity seven days before irrigated plants. Plants of cv. Scylla gave a final TDM of 730 g m⁻²; compared to the 530 g m⁻² produced by T-49. The average growth rate was 7.0 and 5.2 g m⁻² day⁻¹ for Scylla and T-49 respectively (2003-04). Plants receiving 150 kg N ha⁻¹ produced 665 g m⁻² TDM which was 12 % more than was produced by unfertilised plants. The application of 150 kg N ha⁻¹ gave an average growth rate of 6.4 g m⁻² day⁻¹ compared to 5.7 g m⁻² day⁻¹ from plants with no N. Inoculation in the field had no significant effect on TDM in both seasons. Temperature affected growth and DM accumulation. Accumulated DM was highly dependent on cumulative intercepted PAR. Air temperatures below the base temperature (10 °C) affected growth in 2004-05, resulting in plants accumulating just 0.24 g DM MJ⁻¹ PAR during early growth. This increased to 2.26 g DM MJ⁻¹ PAR when the temperature was increased above the base temperature. There was a strong relationship between LAI and intercepted PAR. A LAI of 4.0-4.5 was required to intercept 90-95 % of incident solar radiation. Cultivar significantly (p < 0.001) affected radiation use efficiency (RUE). Scylla had a RUE of 1.02 g DM MJ⁻¹ PAR compared to T-49 at 1.18 g DM MJ⁻¹ PAR. Seed yield was significantly (p < 0.001) affected by cultivar and fertiliser application. Cultivar Scylla produced 467 g m⁻² which was 76 % more than T-49, while a 12 % increase in seed yield was observed in N fertilised plants over unfertilised plants. Only cultivar significantly affected HI, while the yield components that had the greatest effect on seed yield were hundred seed weight and pods plant⁻¹. Inoculation significantly (p< 0.05) affected 100 seed weight (2004-05). Plants inoculated with strain H 20 had the highest 100 seed weight at 25.2 g with cv. Scylla producing larger seeds than T-49. The belief that local environmental conditions play a major role on field survival of bacteria, led to the use of PCR methods to identify field nodulating organisms. Amplification of genomic DNA from parent isolates using primers fC and rD generated a single band for each isolate. Isolates were identified to the species level as either Rhizobium or Agrobacterium, using the highly conserved internally transcribed spacer (ITS) region and are known to nodulate common bean. The DNA extracted from the isolates recovered from nodules of field grown beans gave multiple bands with primers fC and rD. Five distinct banding patterns were observed. All of these were different from those of parent isolates. Sequencing of the 16S rRNA demonstrated that nodules of field grown beans in Canterbury were inhabited by Pseudomonads either alone or in association with other root nodulating organisms. The inability to identify the inoculant strains in nodules of field grown beans does not rule out their infection and nodulating function in the cultivars used. The results suggest the possibility of both Rhizobium and Pseudomonads cohabiting in the nodules of field grown beans. The aggressive nature of Pseudomonads on artificial media, possibly out competing the inoculant rhizobia is proposed, leading to the inability to identify the inoculant strain from the nodules of the field grown beans by PCR methods. The need to identify the nodule forming or nodule inhabiting bacteria in the nodules is necessary to classify the importance of these organisms and their economic benefit to agricultural production. This study also underlines the importance of using PCR methods to gain valuable insights into the ecological behaviour of Rhizobium inoculants and nodule inhabiting organisms.

This thesis is presented in the form of a series of papers some of which have already been published. It is prefaced by a review of research on the agronomy and physiology of wheat yield in New Zealand, and concluded with a general discussion, Other relevant papers in which the author was a contributor may be found in the Appendix. / Between 1972 and 1976 a series of field experiments were conducted to investigate the factors limiting grain yield in wheat (Triticum aestivum L). Spike population restricted yield when it was below about 500 spikes/m² but once it exceeded 700/m² grain yield declined due to a reduction in the number of grains per spikelet. Irrigation, high sowing rate, and nitrogen fertiliser generally increased spike number but the effects on the number of grains/spikelet were variable, apparently depending on processes related to leaf area index. The semi-dwarf Karamu outyielded New Zealand wheats when spring-sown because it produced more spikelets/spike and more grains/ spikelet than the other cultivars. The superior grain set of Karamu was because more of the distal florets within each spikelet produced grain than in the other cultivars. The results are discussed in relation to cultural practices and plant breeding.

The vegetative and reproductive development of balansa clover (Trifolium michelianum Savi.) were quantified in relation to the environmental drivers of each phenophase in field and controlled environments. In a grazed experiment over 6 years, balansa clover sown with cocksfoot (Dactylis glomerata) contributed 1.6 t DM/ha/year, or ~20% of the total DM production. However, grazing management for increased seed production during flowering in the establishment year strongly influenced balansa clover regeneration. The earliest closed plot (September) averaged between 2.2 and 4.3 t DM/ha/year of balansa clover across all six years. In an incubator, balansa clover required 29°Cd for germination with an optimum temperature of 14°C and a maximum of 40°C. The base temperature for germination was 0°C. A field experiment determined that 38°Cd were required for emergence with an optimum soil temperature (Topt) of 8.5°C. The time from emergence until the first leaf appeared, the phyllochron and timing of axillary leaf appearance were compared with perennial ryegrass (Lolium perenne) and white clover (Trifolium repens L.). The rate of each was found to increase linearly with temperature. The balansa clover cultivar ‘Frontier’ required 97°Cd from sowing for the first leaf to appear, had a phyllochron of 47°Cd and secondary leaves appeared after 490°Cd. For each vegetative stage, the base temperature was 2.5°C. The timing of flower appearance depended on the quantity and direction of change of the photoperiod at emergence. A balansa clover plant, cv. ‘Bolta’, which emerged on 1 December into an increasing photoperiod of 15.6 hours flowered after 574°Cd (Tbase = 2.5°Cd) or 58 days after emergence. In contrast, if the plant emerged on 16 January into a similar but decreasing photoperiod it took 1503°Cd or 227 days to flower. This length of time became progressively shorter until remaining constant after the shortest day. In contrast, ‘Frontier’ took a constant 390 and 690 °Cd in increasing and decreasing photoperiods, respectively. The time which an individual inflorescence took from pollination until seeds were physiologically mature was 250 °Cd for both ‘Bolta’ and ‘Frontier’. The re-establishment of balansa clover each year relied on a large seed set (>1000 kg/ha) in the establishment year. The continued survival of balansa clover would then depend on a similar seeding event within a 4-5 year period to maintain the seed bank. Management considerations for balansa clover persistence and survival are discussed.

The permanent pasture based on a grass-clover association and utilised in situ by grazing stock is the basis of New Zealand's chief primary industries. Although white clover is the main legume species used for this purpose its production and persistence in the drier eastern areas of the South Island often leaves much to be desired. In such situations subterranean clover may provide a useful alternative. Subterranean clover has been a very useful species in the past and will probably continue to play an important role in the future, provided the most climatically adapted cultivars are grown. The aim of the field trials was to evaluate the productive performance of several subterranean clover cultivars in Canterbury. Because of the big influence of seed yield on subsequent production and persistence in annuals, this aspect was also investigated. The subterranean clover cultivars Geraldton, Yarloop, Woogenellup, Clare, Mt. Barker and Tallarook were evaluated under cutting in swards at two sites in Canterbury.

Despite the importance of a high white clover (Trifolium repens) content in temperate pastoral systems in terms of livestock performance and nitrogen fixation, the proportion of white clover in grass-clover pastures is often low (<20%). This thesis examined in two experiments whether the white clover content of pastures could be improved by sowing white clover with alternative grass species to diploid perennial ryegrass (Lolium perenne L.). In a pasture experiment, DM production, pasture composition and morphology of grass-clover mixtures was measured over the establishment year (January 2007 to January 2008) where white clover was sown in fine mixtures with diploid perennial ryegrass, tetraploid perennial ryegrass, timothy (Phleum pratense L.) and cocksfoot (Dactylis glomerata L.). Pastures were irrigated and rotationally grazed with on-off grazing with Coopworth ewe hoggets. Total annual DM production of pasture was more than 20% higher in tetraploid (12521 kg DM ha⁻¹) and diploid (11733 kg DM ha⁻¹) perennial ryegrass than timothy (9751 kg DM ha⁻¹) and cocksfoot (9654 kg DM ha⁻¹). However, timothy (5936 kg DM ha⁻¹) and cocksfoot (5311 kg DM ha⁻¹) had more than four times higher white clover annual DM production than tetraploid (1310 kg DM ha⁻¹) and diploid (818 kg DM ha⁻¹) ryegrass. Pasture growth rate at the first three harvests in autumn was significantly greater in tetraploid and diploid ryegrass than timothy and cocksfoot. Timothy and cocksfoot had a higher proportion of white clover than tetraploid and diploid perennial ryegrass throughout the entire year. This was due to more and larger white clover plants in timothy and cocksfoot plots. In a grazing preference experiment, the partial preference of sheep for white clover offered in combination with the same grass species as in the pasture experiment was measured in five grazing tests in May, September, October, November and December 2007. Pastures were sown in January 2007. Paired plots (grass and clover both 4.2 m x 10 m) were grazed by three Coopworth ewe hoggets between 9am and 5pm, and preference was recorded by decline in pasture mass and visual scan sampling for grazing time. Grazing preference for clover was generally low throughout these tests (e.g. average apparent DM intake from clover = 47%; average grazing time from clover = 44%). Several explanations are proposed for this low preference including a high N content and intake rate of the grass relative to the clover. No significant differences were found among the grass treatments in total grass grazing time, total clover grazing time, ruminating time, the proportion of grazing time on clover, selective coefficient for clover and DM intake percentage from clover at any date. There was no significant change in overall sward surface height (SSH) decline among grass treatments throughout all the tests except December 2007 when the overall SSH decline for cocksfoot was significantly lower than the other species. The study indicated that the rapid growth rate of perennial ryegrass in the early phase of pasture establishment, rather than differences in partial preference, was the key factor limiting white clover content in the mixed swards relative to cocksfoot and timothy pastures. It is concluded that high clover-containing pastures capable of delivering high per head performance can be established through the use of slow establishing pasture species such as timothy and cocksfoot.

This study consisted of two sheep grazed dryland pasture experiments. Experiment l compared sheep production from 3-year-old cocksfoot based pastures grown in combination with white, Caucasian, subterranean or balansa clover with a ryegrass-white clover pasture and a pure lucerne forage. Sheep liveweight gain per head from each pasture treatment and the pure lucerne stand was recorded in the 2006/07 and 2007/08 seasons. The cocksfoot-subterranean clover pasture provided equal (381 kg LW/ha in 2006) or higher (476 kg LW/ha in 2007) animal production in spring and gave the highest total animal production (646 kg LW/ha) averaged across years of the five grass based pastures. However, total annual liveweight production from lucerne was higher than any grass based pasture mainly due to superior animal production during summer when lucerne provided 42-85% higher animal production than any of the grass based pastures. In Experiment 2, the effect of stocking rate (8.3 (low) and 13.9 (high) ewes + twin lambs/ha) and time of closing in spring on lamb liveweight gain, pasture production and subterranean clover seedling populations was monitored over 2 years for a dryland cocksfoot-subterranean clover and ryegrass-subterranean clover pasture in Canterbury. In both years, twin lambs grew faster (g/head/d) in spring at low (327; 385) than high (253; 285) stocking rate but total liveweight gain/ha (kg/ha/d) was greater at high (7.26; 7.91) than low (5.43; 6.38) stocking rate. Ewes also gained 0.5 and 1.5 kg/head at the low stocking rate in 2006 and 2007 respectively but lost 0.2 kg/head in 2006 and gained 0.3 kg/head at high stocking rate in 2007. Mean subterranean clover seedling populations (per m²) measured in autumn after grazing treatments in the first spring were similar at both low (2850) and high (2500) stocking rate but declined with later closing dates in spring (3850, 2950, 2100 and 1700 at 2, 4, 6, 8 weeks after first visible flower). Seedling populations measured in autumn after grazing treatments in the second spring were also unaffected by stocking rate (low 1290, high 1190) but declined with later closing dates in spring (1470, 1320 and 940 at 3, 5 and 8 weeks after first flowering, respectively). The effect of stocking rate and closing dates in spring on pasture and clover production in the following autumn was similar to the effects on seedling numbers in both years. However, clover production in the following spring was unaffected by stocking rate or closing date in the previous year at the relatively high seedling populations generated by the treatments. This was presumably due to runner growth compensating for lower plant populations in pastures that were closed later in spring. Subterranean clover runner growth in spring may not compensate in a similar manner if seedling numbers in autumn fall below 500/m². Mean annual dry matter production from cocksfoot and ryegrass pastures grown with and without annual clovers pasture production ranged from 6.4 to 12.4 t DM/ha/y but stocking rate (8.3 vs. 13.9 ewes/ha) during spring did not affect annual pasture production. Pastures overdrilled with annual clovers yielded 23-45% more dry matter production than pastures grown without annual clovers. The study confirms the important role of subterranean clover in improving pasture production and liveweight gains of sheep in dryland cocksfoot and ryegrass pastures. Lowering stocking rate from 13.9 to 8.3 ewes/ha was a less effective method of increasing seed production of subterranean clover in dryland pastures although it did lead to increased liveweight gain per head.