Field Pea Seeding Management for Semi-arid Mediterranean Conditions

The effects of seeding rate (30, 60 and 90 seeds m^?2), seeding date (14 January, 28 January and 12 February), seed weight (0.18 and 0.25 g seed^?1), seeding depth (3 and 6 cm), and phosphorus fertilization rate (17.5, 35.0 and 52.5 kg P ha^?1) and placement method (banded or broadcasted) on field pea (Pisum sativum L.) development and seed yields were investigated in irrigated field experiments conducted in northern Jordan in 2000 and 2001. Results and treatment responses were consistent in both years. Seeding rate, seeding date, seed weight and rate and method of phosphorus fertilization had significant effects on most traits measured; planting depth however did not affect any of the traits. Generally a positive correlation was observed between each factor and seed yield and yield components, with the exception of a negative correlation between seeding rate and yield components, and seeding date and yield and yield components. Increase in seeding rate from 30 to 90 seeds m^?2, and increase in P fertilization from 17.5 to 52.5 kg ha^?1 alone increased seed yields by 50 and 41 %, respectively. Each delay of 2 weeks for seeding from mid‐January resulted in reductions of 12 % in seed yields. Overall, the results revealed that a combination of early seeding (14 January), of large seeds at an high seeding rate (90 seeds m^?2), with P fertilizer banding (52.5 kg P ha^?1) maximize field pea yields in irrigated fields in semi‐arid Mediterranean environments. With such management pea seed yields can be as high as 2800 kg ha^?1.     

Effect of Planting Date and Thermal Energy Intensity on Rate of Phosphorus and Potassium Accumulation by Maize (Zea mays L.)1

The effect of planting date and thermal energy intensity (TEI) on the rate of phosphorus (P) and potassium (K) accumulation by maize from a Hamerly clay loam soil (Aerie Calciaquoll) was examined with and without supplemental irrigation. Soil- and air-TEI expressed as growing degree days per day (GDD d^?1) were determined from hourly temperature measurements taken within each plot. Net K accumulation occurred during the vegetative growth stage, reached maximal rates of about 62.2 to 91.4 mg plant^?1 day^?1, and attained maximal accumulations ranging from about 1.15 to 2.3 g plant^?1. Accumulation of P occurred during vegetative and reproductive growth stages, reached maximal rates of about 4.6 to 10.3 mg and 6.5 to 12.1 mg plant^?1 day^?1, respectively and maximal accumulations of 0.175 to 0.27 g and 0.11 to 0.26 g plant^?1, respectively. During vegetative growth, K and nitrogen (N) accumulation characteristics were closely correlated with about 2 moles of N accumulated per mole of K. Maximal accumulation of K (and N) consistently preceded that of P by about 5.2 to 8.3 days and that of the plant dry weight by about 15.9 to 20.5 days during the vegetative growth stage. Time required to reach maximal accumulation during the reproductive growth stage, t_r followed the order N < P < dry weight for early plantings and followed the order N < P < dry weight for delayed plantings. Time coefficients for K and P accumulation were correlated closely with soil-TEI, but models of each coefficient relied on unique combinations of TEI. Time coefficients for dry matter accumulation were apparently unrelated to soil- or air-TEI.     

Salt Stress Delayed Flowering and Reduced Reproductive Success of Chickpea (Cicer arietinum L.), A Response Associated with Na+ Accumulation in Leaves

Salinity is known to reduce chickpea yields in several regions of the world. Although ion toxicity associated with salinity leads to yield reductions in a number of other crops, its role in reducing yields in chickpea growing in saline soils is unclear. The purpose of this study was to (i) identify the phenological and yield parameters associated with salt stress tolerance and sensitivity in chickpea and (ii) identify any pattern of tissue ion accumulation that could relate to salt tolerance of chickpea exposed to saline soil in an outdoor pot experiment. Fourteen genotypes of chickpea (Cicer arietinum L.) were used to study yield parameters, of which eight were selected for ion analysis after being grown in soil treated with 0 and 80 mm NaCl. Salinity delayed flowering and the delay was greater in sensitive than tolerant genotypes under salt stress. Filled pod and seed numbers, but not seed size, were associated with seed yield in saline conditions, suggesting that salinity impaired reproductive success more in sensitive than tolerant lines. Of the various tissues measured for concentrations of Cl^?, Na⁺ and K⁺, higher seed yields in saline conditions were positively correlated with higher K⁺ concentration in seeds at the mid‐filling stage (R² = 0.55), a higher K⁺/Na⁺ ratio in the laminae of fully expanded young leaves (R² = 0.50), a lower Na⁺ concentration in old green leaves (R² = 0.50) and a higher Cl^? concentration in mature seeds. The delay in flowering was associated with higher concentrations of Na⁺ in the laminae of fully expanded young leaves (R² = 0.61) and old green leaves (R² = 0.51). We conclude that although none of the ions appeared to have any toxic effect, Na⁺ accumulation in leaves was associated with delayed flowering that in turn could have played a role in the lower reproductive success in the sensitive lines.     

Response of pea (Pisum sativum L.) to mepiquat chloride under varying application doses and stages

Grown as a monoculture, peas (Pisum sativum L.) exhibit severe lodging after flowering and lodging causes yield reductions considerable. This study was conducted to investigate the effects of dose (untreated, 25, 50, 75 and 100 g a.i. ha^?1) and stage (late vegetative, early blooming and early pod filling) of mepiquat chloride (MC) application on the growth, lodging control, seed yield and yield parameters of pea (Pisum sativum L.) under field conditions in Erzurum, Turkey in 2002 and 2003. Application doses of 25, 50, 75 and 100 g a.i. ha^?1 significantly reduced stem height by 5.3 %, 7.2 %, 7.5 % and 6.4 % and increased stem width by 7.5 %, 12.7 %, 12.3 % and 15.7 % respectively, when compared with the untreated control, and thereby reduced the tendency of the crop to lodging. Increases of the seed yield under different application doses of MC ranged between 13.7 % and 20.1 % over the untreated control. However, in all parameters investigated, except for stem width, higher application doses of MC gave no clear advantages compared with the application dose of 25 g a.i. ha^?1. Seed yield was also significantly influenced by application stage of MC and application at early blooming stage of crop, MC significantly increased seed yield by 11.4 % and 10.2 % when compared with the late vegetative and the early pod filling stages respectively. Furthermore, the interaction of application dose and stage was significant, and spraying of pea plants with 25 g a.i. ha^?1 MC at early blooming stage has the most beneficial effects on the characters evaluated.     

Effects of Salinity and Soil–Drying on Radiation Use Efficiency,Water Productivity and Yield of Quinoa (Chenopodium quinoa Willd.)

Drought and salinity reduce crop productivity especially in arid and semi‐arid regions, and finding a crop which produces yield under these adverse conditions is therefore very important. Quinoa (Chenopodium quinoa Willd.) is such a crop. Hence, a study was conducted in field lysimeters to investigate the effect of salinity and soil–drying on radiation use efficiency, yield and water productivity of quinoa. Quinoa was exposed to five salinity levels (0, 10, 20, 30 and 40 dS m^?1) of irrigation water from flower initiation onwards. During the seed‐filling phase the five salinity levels were divided between two levels of irrigation, either full irrigation (FI; 95 % of field capacity) or non‐irrigated progressive drought (PD). The intercepted photosynthetically active radiation was hardly affected by salinity (8 % decrease at 40 dS m^?1) and did not differ significantly between FI and PD. Radiation use efficiency of dry matter was similar between salinity levels and between FI and PD. In line with this, no negative effect of severe salinity and soil–drying on total dry matter could be detected. Salinity levels between 20 and 40 dS m^?1 significantly reduced the seed yield by ca. 33 % compared with 0 dS m^?1 treatment owing to a 15–30 % reduction in seed number per m², whereas the seed yield of PD was 8 % less than FI. Consequently, nitrogen harvested in seed was decreased by salinity although the total N‐uptake was increased. Both salinity and drought increased the water productivity of dry matter. Increasing salinity from 20 to 40 dS m^?1 did not further decrease the seed number per m² and seed yield, which shows that quinoa (cv. Titicaca) acclimated to saline conditions when exposed to salinity levels between 20 and 40 dS m^?1.     

Yield Variation of Soybeans in Hawaii

In Hawaii, soybeans planted in November through January will produce yields of 25 to 50 percent compared with those planted through June. Yield components were studied for several soybean cultivars to determine which one was the most sensitive to planting dates and if there were differences between cultivars.
Soybean cultivars, Amsoy 71, Davis, Forrest, Kahala, P.I. 297,550 , and Williams were planted each month for two years. One November planting was lost, so there were 23 tests representing different environments. Each test consisted of 24 plots, six cultivars in four replications in a randomized block.
Analysis of variance of combined tests indicated significant differences between number of plants, pods per plant, seeds per pod, seed weight, yield of seed, plant height, and oil content of the seed that were due to data of planting, cultivar, and date × cultivar interaction.
Regression analysis indicated a closer relationship between pods per plant and yield during stress conditions (November through January plantings), whereas number of seeds per pod was more closely associated with yield during non-stress environments (April through June plantings).     

Seed Yield Stability of Okra as Influenced by Planting Date

Fifteen selected okra varieties consisting of ten newly-developed lines and five established varieties were evaluated for stability of seed yields in eight different environments i.e. several monthly plantings for three consecutive years. Seed yield data were analyzed to determine the effectiveness of using different planting dates in seed yield trials of new okra varieties. The wide ranges of environmental indices (- 10.8 to 24.4) and seed yield (2.7 to 38.0 g plant ^-1) indicated significant variation between the environments even though the trials were conducted at the same location. A regression method of stability analysis showed that the mean differences between environments, the varieties and their interactions were highly significant. These results suggest that where limited resources prevent the use of several locations, different dates of planting for two or more years could be used to evaluate okra varieties for seed yield without losing much information on their relative ranking.     

Effect of Planting Date on Time and Rate of Nitrogen Accumulation by Maize (Zea mays L.)1

Effects of environment on time and rate of nutrient accumulation by crops affects fertilizer nutrient use efficiency. The effect of planting date on rate, time and amount of nitrogen (N) accumulated by maize from a Hamerly cl soil (Aeric Calciaquoll) was examined with and without supplemental irrigation. Maize was planted on three dates spaced at 2-to 3-week, intervals; the earliest planting date was 1 May in 1984 and 1985. N accumulation was examined as uni- and diphasic tanh[k(time)] functions and solved for total N accumulation at harvest, time of maximum N accumulation rate and the time coefficient of N accumulation. A diphasic function, which indicates two periods of intense N accumulation, provided the closest agreement with observed N accumulation. As planting was delayed, time required to reach maximum N accumulation rates, τ (uniphasic) or τ₁ and τ₂ (diphasic), decreased from an average of nearly 75 to 42 days (uniphasic) and from nearly 65 to 35 days and 100 to 75 days after planting for τ₁ and τ₂, respectively. Maximum N accumulation rates increase from about 59 to 75 mg N plant^?1 day^?1 (uniphasic) or 35 to 65 mg N plant^?1 day^?1 and 20 to 70 mg N plant^?1 day^?1 for the first and second maxima in the diphasic model, respectively. Average maximum total N accumulation ranged from 2.85 g N plant^?1 for early plantings to 1.5 g N plant^?1 for plantings made on 25 June. The time coefficient, k (uniphasic) or k₁ (diphasic), tended to increase from average values of about 0.04 to > 0.09 day^?1 for k and from about 0.04 to > 0.105 day^?1 for k₁. The second time coefficient, k₂, of the diphasic function varied widely between about 0.075 to > 0.12 day^?1 and showed complex relationships with planting date. Periods of N accumulation shortened and intensity of N accumulation increased as the time coefficient increased.     

The Influence of Row Spacing and Seeding Rate on Seed Yield and Yield Components of Forage Turnip (Brassica rapa L.)

The effects of four row spacings (17.5, 35.0, 52.5 and 70.0 cm) and five seeding rates (50, 100, 200, 400 and 800 viable seeds m^?2) on seed yield and some yield components of forage turnip (Brassica rapa L.) were evaluated under rainfed conditions in Bursa, Turkey in the 1998–1999 and 1999–2000 growing seasons. Plant height, stem diameter, pods/terminal raceme, total pods/plant, seeds/pod and primary branches/plant were measured individually. The number of plants per unit area was counted and the lodging rate of the plots was scored. The seed yield and 1000‐seed weight were also determined. Row spacing and seeding rate significantly affected most yield components measured. The number of plants per unit area increased with increasing seeding rate and decreasing row spacing. Plant height was not greatly influenced by row spacing and seeding rate, but higher seeding rates reduced the number of primary branches and the stem diameter. The number of pods/main stem was affected by row spacing and but not by the seeding rate. Also, the number of seeds per pod was not affected by either the row spacing or the seeding rate. In contrast, the number of pods per plant clearly increased with increasing row spacing, but decreased with increasing seeding rate. The plots seeded at narrow row spacings and at high seeding rates were more sensitive to lodging. Seeding rate had no significant effect on seed yield in both years. Seed yield was similar at all seeding rates, averaging 1151 kg ha^?1. However, row spacing was associated with seed yield. The highest seed yield (1409 kg ha^?1) was obtained for the 35.0‐cm row spacing and 200 seeds m^?2 seeding rate combination without serious lodging problems.     

Effect of Soil Hydrothermal Regimes on the Performance of Safflower Planted on Different Dates

Soil hydrothermal regimes which can enhance seed germination, seedling emergence and development so that the late planted safflower (Carthamus tinctorius L.) can be competitive in comparison to normally planted crop need to be studied and suitabily modified. Therefore, a split-plot held experiment was conducted in Vertisols during 1984–85 and 1985–86 post-rainy season to determine the influence of planting date (PD₁: Oct. 20; PD₂: Oct. 30; PD₃: Nov. 10; PD₄: Nov. 20; PD_s: Nov. 30; PD₆: Dec. 10; and PD₇: Dec. 20), irrigation (I₁: come-up irrigation and I₂: I₁+ branching stage) and straw-mulch (M₀: No mulch and M₁: paddy straw mulch at 10 t ha^-1) and the interaction on the growth and development of safflower (Cultivar, JSF-7). Germination of safflower commenced earlier in October planting, but it was significantly higher in November and December plantings. Initiation of emergence and completion of germination required 153 and 307 cumulative degree days (CDD soil), respectively. Days to maturity decreased from 163 to 140 in 1984–85 and from 156 to 137 in 1985–86 with delay in planting from October to December. Height, number of branches, number of capsules, seed yield per plant and 1000 seed weight were significantly affected by the different treatments. Planting of safflower on October 30 and November 10 in both the seasons produced significantly higher seed yield than the other plantings. Branching stage irrigation (I₂) and straw mulching significantly improved all the yield attributes and seed yield of safflower in both the seasons. The water use efficiency (WUE) was higher in early plantings than in the later plantings. Higher WUE was obtained under come-up irrigation. Straw mulching increased the WUE, moderated the diurnal variations in soil temperature and provided a better thermostable regime more congenial for plant roots which resulted in increased safflower seed yield.     

Efficiency of water use of early plantings of sunflower

Rain fed crop production in Mediterranean environments depends to a large extent on strategies that avoid the intense summer drought. Early plantings of sunflower have given consistently higher yields in such environments, but the basis for such yield increases has not been explored. We conducted two field experiments at Cordoba (Spain) to investigate the effects of an early and a late planting date on the components of water-limited crop productivity; namely, water use (T), water use efficiency (TE) and harvest index (HI) of sunflower. The results were generalized by simulating rain fed sunflower yields, under early (1 January) and late (15 March) plantings, for a 25-year period with the aid of a simulation model of the Ceres type (OILCROP-SUN) which has been validated in Cordoba. Experimental seed yields of early plantings in 1989 and 1996 were 2.0 and 3.0 t ha⁻¹, while late plantings yields were 1.3 and 2.4 t ha⁻¹, for the 2 years. Average simulated yields were 2.7 ± 1.1 and 1.9 ± 0.7 t ha⁻¹ for early and late plantings, respectively. For the 2 years, T of early plantings was higher than that of late plantings, but the response of TE and HI to planting date was not the same in the two experiments. In the simulation exercise, T and TE of early plantings were consistently higher than those of late plantings, while there were no differences in the HI for the two planting dates. We conclude that early plantings of sunflower increase rain fed yields by increasing both T and TE, while the impact of planting date on HI very much depends on the crop water stress pattern, which is quite variable from year to year even in the predictable Mediterranean environment.     

Yield trade-off and the role of parental selection based on seed size when breeding for soybean seed protein

Alternative physiological strategies can increase protein concentration in soybean: (i) more-than-proportional increases in seed protein content (mg seed⁻¹) relative to increases in carbohydrate and oil content in large-seeded genotypes or (ii) more-than-proportional reductions in carbohydrate and/or oil content relative to protein content reductions in small-seeded genotypes. Because these strategies differentially affect crop growth and development, we hypothesized that populations developed from high-protein (HP) parents with contrasting seed sizes will present differences in how seed yield and protein concentration correlate. To test this, three breeding strategies were developed by mating high-yielding cultivars and HP ones that differ in seed sizes, reflecting the alternative strategies mentioned above. Neither tested crossing strategies showed differences in their correlation values between seed yield and protein concentration, as initially expected. Nevertheless, populations developed from crossing a HP-small-seeded parent to a HP-large-seeded one showed the highest number of transgressive segregants for protein yield. Our results showed that parent selection based on seed size has no beneficial effects on the development of high-yielding, HP soybean populations, but it might affect the number of transgressive segregants for protein yield.     

Reproductive Abscission and Yield of Irrigated and Drought Stressed Cowpea

Two experiments were conducted under field conditions to evaluate reproductive abscission, seed yield and yield components of three cowpea [Vigna unguiculata (L.) Walp.] genotypes. In the first experiment, level of abscission and yield of two cultivars, California Blackeye Pea No. 5 (CA-5) and Speckle Purple Hull (SPH), and one experimental line (AZ-54) were studied. In the second experiment, effect of drought stress on abscission at three nodal positions, seed yield, and yield components of CA-5 were studied. Abscission in both experiments was determined by counting scars left by dropprd reproductive structures including floral buds, open flowers, and immature pods. Abscission of CA-5 and AZ-54 in the first experiment ranged between 68 and 76 % while that of SPH ranged between 86 and 89 %. CA-5 and AZ-54 retained two to three pods per peduncle, and SPH retained only one mature pod per peduncle. Average seed yields of SPH and AZ-54, respectively, were 45 and 50 % of CA-5. Drought stress in the second experiment did not affect production of floral buds Peduncle^?1 (average of 10) but significantly increased percent reproductive abscission and decreased pod retention of CA-5. Abscission in the bottom two-third nodes increased from 82 % in well-irrigated plants to 93 % in non-irrigated plants. This increase in abscission corresponded to nearly 60 % reduction in pod retention. The number of pods per peduncle in the bottom two-third nodes decreased from 1.9 in well-irrigated plants to only. 77 in non-irrigated plants. The increase in abscission and decrease in pod retention with increasing intensity of drought was greatest in the bottom one-third nodes. Drought stress did not affect abscission and pod retention in the top one-third nodes. Stress also decreased peduncles plant^?1, seeds pod^?1, and dry matter and seed yield plant^?1 but did not affect seed weight and harvest index. The decrease in seed yield was largely due to reductions in pods plant^?1 and seeds pod^?1. The reduction in the number of pods and, therefore, seed yield due to stress was because of reductions in the number of peduncles plant^?1 and increases in reproductive abscission. It is concluded external conditions that increase abscission beyond that of normal occurrence affect seed yield adversely.     

Konkurrenz und Ertragsvorteile in Gemengen aus Erbsen (Pisum sativum L.) und Hafer (Avena sativa L.)

In field trials on a fertile fluvisol in 1995 and 1996 near Göttingen, Germany, pea (Pisum sativum; cv. Messire/conventional leafed, cv. Profi/semileafless) and oats (Avena sativa; cv. Alf) were grown as sole crops and in substitutive mixtures. The sole crops were established at 80 pea seeds m^?2 and 300 oat seeds m^?2. The mixtures consisted of 67 % (pea) and 33 % (oats) of the monoculture densities, respectively. Interactions of cv. Messire or cv. Profi and oats were similar in 1995 and 1996. The mixtures outyielded the monocultures with respect to total above ground dry matter (RYT = 1.15) and grain yield (RYT = 1.09). Grain yield of pea and oats averaged 4.9 t ha^?1 in monocultures and 5.5 t ha^?1 in mixtures. Oats was relatively the stronger of the two competitors. Decreasing number of pods per plant could be highlighted as the factor for a lower pea seed frequency in the yield of the mixtures. For oats the number of panicles per plant and kernels per panicle were higher in the mixtures compared with the oat monocultures. The average amount of the harvest index (HI) was 0.52 for pea and 0.46 for oats. Favourable growth conditions increased HI values however, prolific vegetative growth in the mixtures resulted in lower HI values. The predicted RYT‐values estimate the maximum combined grain yield of 6.3 t ha^?1 in the mixture of 87 % pea (70 seeds m^?2) and 13 % oats (39 kernels m^?2).     

Growth and Yield Performance of Some Cotton Cultivars in Xinjiang,China, An Arid Area with Short Growing Period

Eleven cotton (Gossypium hirsutum L.) cultivars were evaluated for their growth and yield performance in Shihezi, Xinjiang, China, an area in Central Asia with short growing period in 1999 and 2000. In each cultivar the number of bolls per plant was low and the number of bolls per unit area was high. Each cultivar showed rather high seed and lint yields. The highest lint yield was Xinluzao 10 in both years with 1761 and 1809 kg ha^?1. High yield ability of the cultivars in this study was attributed to large number of bolls per unit area with high lint percentage. Seed and lint yields had significant positive correlations with mean net assimilation rate, ratio of reproductive to vegetative organs and mean boll weight at earlier stages of boll growth, suggesting that early boll formation and successive partitioning of dry matter into bolls were important factors for boll growth in this study area.     

Management of Italian and Perennial Ryegrasses for Seed and Forage Production in Crop Rotations

Italian ryegrass (Lolium multiflorum Lam.) and perennial ryegrass (L. perenne L.) can be grown for seed and forage in cold winter regions provided the stand persists well over winter. Seed yield and plant characteristics during primary growth, and forage yield during regrowth, were determined for two Italian and one perennial ryegrass cultivars in Atlantic Canada. Establishment methods and dates included sowing ryegrass in cultivated soil alone or with barley in mid‐May and, after harvesting the barley crop, by sowing ryegrass following conventional or reduced cultivation and by no‐till drilling into barley stubble in mid‐August and early September. Despite some winterkill, particularly in Italian ryegrass, seed and forage yields were adequate in post‐establishment growing seasons. Seed yield for Italian ryegrass was greatest (1270 kg ha^?1) when it was sown into cultivated soil in mid‐August and least (890 kg ha^?1) when sown alone in May. Italian ryegrass yielded 15–17 % more seed when plots were established in mid‐August rather than in mid‐May or early September. Italian ryegrass cv. Lemtal had a greater density of fertile tillers (1030 m^?2) in the sward than cv. Ajax (860 m^?2) and its tiller density was greater when seeded into cultivated soil in September than in mid‐August. There were fewer spikelets per seed head for sowing Italian ryegrass with barley in May than for the other methods of establishment. Forage yield in regrowth was greater for Italian ryegrass cv. Ajax (2770 kg ha^?1) than for cv. Lemtal (2480 kg ha^?1). Seed yield of perennial ryegrass was greater when seeded in mid‐May than in mid‐August or early September. The seed yield of perennial ryegrass was greater when it was sown with barley in May and harvested for grain, than when it was sown alone or with barley harvested at late milk stage. The establishment methods for mid‐August and early September sowing had little effect on seed yield. However, the no‐till and reduced tillage methods resulted in a greater tiller density than sowing into the cultivated seedbed. Fertile tillers tended to be denser under reduced cultivation for sowing in August. Forage yield of perennial ryegrass regrowth was not influenced by the sowing method and timing. In conclusion, Italian and perennial ryegrasses produce adequate seed and forage regrowth under different establishment methods and timing. However, the poor persistence of Italian ryegrass may limit commercial production after the establishment year in Atlantic Canada.     

Maize Grain Yield Response to Tillage and Fertilizer Nitrogen Rates on a Tara Silt Loam

Effects of tillage on the appropriate fertilizer N applications needed to achieve maximal grain yield are poorly denned. The study objective was determination of relative corn grain yield response to N application rate for four tillage practices: no-tillage (NT), ridge tillage (RT), fall chisel plowing (CP) and fall moldboard plowing (MP). Maize (Zea mays L.) grain yield and N accumulation were monitored over a 6 year period with the same tillage treatment and the same fertilizer N rate applied each year to each plot. Two hybrids, differing in relative maturity rating, were planted each year. Fertilizer N rates ranged from 10 to 190 kg ha^?1 and consisted of 10 kg ha^?1 of liquid starter N applied at planting with varying amounts of fall applied anhydrous ammonia. With only starter fertilizer, grain yields increased with tillage intensity in the order NT ≤ RT ≤ CP ≤ MP. With ≥ 55 kg total applied Nha^?1, 6 year average grain yields were unaffected by tillage. Total N removed in grain annually with only starter fertilizer ranged from 25–85 kg ha^?1 Maximal amounts of N removed, about 145 kg N ha^?1, occurred with 100–145 kg applied N ha^?1 for all tillage treatments under the more favorable climatic conditions. Several interactions affecting grain yield appear climatically sensitive with exception of tillage by fertilizer N interactions. Because of variability in climate, planting dates varied by almost 4 weeks. Relative yield loss due to planting delay were Fertilizer N (mean change ??124 –?275 kg ha^?1 day^?1) > Starter N only and MP (mean ?? 259 kg ha^?1 day^?1) > other tillages in general. Yield loss due to delayed planting ranged from 0.0–275 kg ha^?1 day^?1. Grain yield gains due to early spring soil temperatures were 16.0–21.8 kg ha^?1 index-degree^?1 with MP tillage and averaged 2.7– 16.7 kg ha^?1 index-degree^?1 more than those of other tillage-hybrid combinations.     

Effect of Different Preceding Crops and Crop Rotations on Yield of Winter Oil-seed Rape (Brassica napus L.)

To determine the effect of different preceding crops and crop rotations on the grain yield of oil-seed rape, a long-term rotation experiment was conducted at the Hohenschulen experimental station in Kiel, NW Germany. Additional factors included the nitrogen fertilization and the fungicide application. The results reported herein are based upon the harvest years 1988 to 1993. Averaged over the different rotations and husbandry treatments, the grain yields in the 6 experimental years varied between 2.71 t ha^?1 and 3.99 t ha^?1. In contrast, the effect of the different husbandry treatments was smaller and non significant. Averaged over 6 years, only the fungicide application caused small yield increase of 0.2 t ha^?1. The highest grain yields of 3.77 t ha^?1 or 3.65 t ha^?1 occurred when oil-seed rape was directly following peas. Low yields between 3.15 tha^?1 and 3.33 tha^?1 were obtained when oil-seed rape was grown after oilseed rape. The lowest grain yield of 3.13 t ha^?1 was produced with oil-seed rape grown in monoculture only. In rotations with oil-seed rape following a preceding cereal crop (wheat or barley), the grain yields averaged between 3.22 tha^?1 in a two course rotation and up to 3.44 tha^?1 in a four course rotation. In general, the yields of oil-seed rape increase with the length of the rotation and the length of the break between two oilseed rape crops. The yield component number of seeds per m² was affected by the previous cropping accordingly, whereas the thousand seed weight did not respond to the cropping history. Based upon disease assessments in the first years of this experiment, we argue that an increase in the incidence of fungal diseases has considerably contributed to the yield decrease of oil-seed rape in short rotations.     

基于图像处理的冬小麦植被覆盖率测定及其遗传解析

植被覆盖率是反映植株生长势的重要生理性状,在旱作地区尤为重要。图像处理技术能够快速有效地对苗期和孕穗期植被覆盖率进行量化分析。以28份山东小麦主栽品种和品系为材料,在240株 m^-2和360株 m^-2密度下,连续2年测定了孕穗前不同发育阶段的植被覆盖率,并利用921个DArT标记和83个SSR标记分析了与植被覆盖率相关的遗传区段。结果表明。不同密度下,冬小麦植被覆盖率在越冬期、返青期和孕穗期存在显著差异,而起身期基本一致。起身期植被覆盖率与春季最高分蘖数、抽穗后群体叶面积指数、单位面积穗数和籽粒产量均呈显著正相关,r = 0.73~0.76 (P<0.01),表明起身期植被覆盖率可用于预测上述性状。共检测出12个遗传区段与植被覆盖率相关联,大部分区段直接参与调控苗期和孕穗期的生长势。10个遗传区段与已报道的苗期性状、产量性状及抗病位点一致,其中5BL、6AS和6BL染色体上携带的植被覆盖率相关遗传区段与已报道的苗期比叶面积和生物量等位点完全相同。建议将植被覆盖率作为生长势量化指标,用于育种选择和遗传研究。     

Effects of Temperature and Photoperiod on Days to Flowering, Yield and Yield Components of Lupinus albus (L.) under Field Conditions

A better understanding of the agronomic importance of planting date and the influence of cold temperatures and photoperiod during germination and plant growth may lead to better management strategies for cultivation of the sweet white lupin (Lupinus albus). The effects of planting date (temperature and photoperiod) were determined on the number of days to flowering, yield and yield components of four early to medium and one late sweet white lupin genotype in a field trial at Potchefstroom, South Africa, planted during February 1996 to January 1997. Moisture stress was avoided through regular irrigation. Duration of the developmental phases planting date to emergence, emergence to floral initiation, initiation to first flower, duration of flower and days to physiological and harvest maturity was related to field measurements of temperature and photoperiod. Differences in the main determinants of yield, i.e. seeds per pod, pods per plant, single seed mass (SSM), plant and pod height and yield, were measured. Results showed that both temperature and photoperiod influence the growth and development of the Lupinus albus genotypes ‘Esta’, ‘Hantie’, ‘Tifwhite’, ‘Kiev’ and ‘LAL 186’. Temperature influences include the effect of vernalization at seedling emergence. Minimum grass temperatures under 5 °C at emergence are effective for vernalization. However, after grass temperatures at emergence increased again from June to December, to gether with an increase in the photoperiod length, ‘Tifwhite’ as well as the other genotypes still flowered earlier, confirming that these cultivars are long‐day plants, which is in accordance with controlled‐environment data. Cool vernalizing temperatures thus not only influence obligate vernalization requiring genotypes such as ‘Tifwhite’, but also influence the non‐obligate genotypes studied. Plan‐ting date had a significant influence on pods per plant, single seed mass (SSM) and seed yield. In all trials laterplanting, from June to November, decreased SSM and seed yield. The highest seed yield of 1.5 t ha^?1 was obtained for the 10 June planting date and the lowest average yield of 0.450 t ha^?1 for the 5 November planting date.