The effect of small doses of nematicides on migratory root-parasitic nematodes and on the growth of sugar beet and barley in sandy soils

Smaller amounts of D–D (6–12 gal/acre) (68–135 1/ha) or ethylene dibromide (9 gal/acre) (100 1/ha) than are customarily used to disinfest field soils killed many root-parasitic nematodes (Trichodorus, Pratylenchus, Tylenchorhynchus and Longidorus attenuatus) when injected 6–8 in (15–20 cm) deep during early autumn in rows 10 in (25 cm) apart in well-drained sandy soils. They also increased the yield of sugar beet grown in fields infested with Trichodorus or Longidorus attenuatus, without affecting sugar percentage or juice purity of the roots, and in some places increased the yield of barley grown after the beet. D–D was much less effective when injected 8–12 in deep during late autumn or winter. Increasing nitrogen dressings to the seedbed from 1·5 to 3 cwt/acre (188 to 376 kg/ha) increased sugar beet yield in one field, decreased it in another and decreased juice purity in both. In two other experiments extra nitrogen did not affect sugar beet yield. Even smaller amounts of the nematicides ‘placed’ in the rows, before or after sowing sugar beet in them, killed many of the nematodes and also increased sugar yield. Phytotoxic nematicides can be placed in the rows during autumn, winter or spring but placement is simpler during spring, when the treated rows are indicated by the position of the marks of the tractor wheels left when the nematicide was applied. When applied during autumn or winter, the rows need to be indicated by drilling wheat or grass.     

The effect of partial defoliation on yield of sugar beet

Sugar-beet plants were defoliated during growth in seven experiments from 1968 to 1974 either (1) by removing each leaf as it became fully expanded or (2) by removing with scissors as soon as possible all leaves except certain groups up to leaf 50 , but mainly 6 to 20 , or (3) by treating the growing point chemically or mechanically in an attempt to stop the production of leaves after the twentieth. Removing mature leaves decreased yields considerably, but removing all leaves except 6–20 did not decrease significantly total dry matter yield of the whole plant and in one experiment increased it by 7% and root weight by 15%. Remaining leaves had a greater photosynthetic efficiency as measured by growth analysis and a ¹⁴C0₂ feeding technique because they were less shaded or there was reduced competition for some nutrient or essential growth component. Additional leaves formed beyond the twentieth resulted in a proportionately lower photosynthetic efficiency of all leaves, but attempts to treat the plant to stop production of new leaves beyond the twentieth were inconclusive.     

The effect of beet cyst nematode, Heterodera schachtii, on the yield of sugar beet in organic soils

In ten experiments on commercial sugar-beet crops grown on organic soils in 1984–86, a Genstat programme was used to examine the relationship between the initial population of Heterodera schachtii and sugar-beet root yield using the equation
Y = Ymin + (Ymax - Ymin) Z^pi-T
Fixing T = 200 eggs + juveniles 100 g^-1 soil and Z^T= 0.95, estimated values of Ymax varied from 49.2–67.1 t ha^-1 (129– 155% of the national average root yield for the years in which the experiments were carried out) and estimates of Ymin varied from 14.5–53.9 t ha^-1 (27–94% of Ymax). The estimated average root yield loss caused by the nematode was 6.95 t ha^-1.     

The effect of field margins on the yield of sugar beet and cereal crops

The effect of field margins on the yield of sugar beet, wheat and barley was studied on commercial farms and in a series of field experiments from 1992–1997. There was always a trend of increasing yield from the edge of the field to the centre, with a marked reduction around the ‘tramlines’ and the area where machinery turns. In the studies on commercial farms, headland yield loss varied widely. In sugar beet the headlands yielded 19–41% less than the centre, with a mean reduction of 26%. In cereals the range was 3–19%, with a mean loss of 7%. Headland yield reductions were generally smaller in the field experiments than those found on commercial farms. These headland effects did not move towards the centre of the field when grass margins were planted at the edge of the field; there was no significant effect on the yield of the adjacent crop. The presence of boundary trees had the greatest effect on yield: in the outer 9 m of the field, the area shaded by trees produced 4.4 t ha^-1 of wheat, and the area that was not shaded 8.1 t ha^-1. Turning of machinery also significantly reduced yield, while grazing by rabbits and hares surprisingly had no effect. Following the reform of the Common Agricultural Policy in 1992, the main effect of which was to change from a price support policy to direct payments to producers, farmers in the European Union who produce more than a specified tonnage of ‘eligible crops’ per year, are required to fallow a given percentage of their land (currently 5%), to qualify for Arable Area Payments. Growers can elect to fallow fields on a rotational basis, or permanently. Headland set-aside is a term used to describe strips of set-aside, a minimum of 20 m wide around the edges of fields. In these experiments, the headland effect did not extend beyond 20 m from the field edge. Therefore, particularly in fields with boundary hedges or trees, headland set-aside could effectively remove the poor-yielding area at the field margin.     

Effect of seedling treatment on growth and yield of sugar beet in the field

Sugar-beet seeds were germinated (1) in a growth cabinet at 20°C lit continuously by fluorescent tubes (L), (2) in a cabinet at 20°C lit by fluorescent tubes for 16 h/day (S), (3) in a cage with glass roof and open sides with natural illumination (N), or (4) in the open ground (D). The seedlings from the cabinets and cage were transplanted to the field when they had two true leaves. Samples were taken on six occasions during growth, and leaf areas and dry weights determined. There were no differences between treatments in total number of leaves produced or leaf area duration. Leaf area per plant increased fastest on L plants at first, but from mid-June until end of July drilled plants had the largest leaf surface. From August onwards S plants had the largest area. Although treatment had little effect on growth of the tops, roots grew fastest throughout the season on the plants raised in growth cabinets and the final mean root dry weight of L and S plants was 39% greater than of N and D plants. Throughout the season L and S plants had a larger root:top ratio than plants raised in the cage or drilled directly in the field. The larger roots of plants raised in the cabinets evidently provided a larger sink for carbohydrate and increased the mean photosynthetic efficiency of the leaves over the whole season by 11 % and increased yield of roots by 6 tons/acre.     

The effect of light and temperature late in the season on the growth of sugar beet

Sugar-beet plants were subjected to all combinations of two day temperatures (12-5 and 18-5 ^oC), two night temperatures (8-o and 14-0 ^oC) and two light intensities (275 and 550 J cm-² of visible radiation in a 12 h day) during the last month of their growth. Cold day or night temperatures resulted in the plants having slightly smaller leaf areas, final dry weights and amounts of sugar in their roots than plants grown in warm temperatures. Plants grown in the cold also contained less water, particularly those given cold nights, so that they had smaller fresh weights and a greater concentration of sugar in the fresh, but not in the dry roots, than plants grown in warm conditions. Halving the light intensity had little effect on leaf area but decreased the net assimilation rate. The final dry weight of the shoot was not affected by changing the light intensity, but the dry weights of the roots of plants grown in dim light were 20 % smaller than in plants grown in bright light and they contained correspondingly less sugar. There was no effect of varying the light intensity on the concentrations of sugar in the fresh or dry roots. There was no evidence that cold night temperatures, either alone or in conjunction with bright conditions during the day, induced the storage root to accumulate sugar faster relative to non-sugar dry matter, i.e. to 'ripen'.     

Impact of sugar beet seed priming on seed quality and performance under diversified environmental conditions of germination,emergence and growth

Journal of Plant Growth Regulation - In the presented work attempts have been made to explore effectiveness of the sugar beet (Beta vulgaris L.) seeds priming process in relation to seed quality...     

Some effects, especially on yield, of artificially defoliating sugar beet

The effects of completely defoliating sugar beet at different dates from May to October were examined in four years. In each year there were plots given the usual nitrogen fertiliser application to the seedbed, and also in two of the years plots given no nitrogen. At harvest in mid-November, minimum root weights followed defoliation in July or August, but defoliation in August or later gave minimum sugar contents. When nitrogen was applied to the seedbed sugar yields were smallest after August defoliation; in the absence of nitrogen, July defoliation gave the lowest sugar yields, root yield being smaller but sugar content usually greater than with nitrogen. Up to 40% of the sugar yield was lost by July or August defoliation and late defoliation increased some of the impurities in the root juice. Yields, and recovery from defoliation, were greater with nitrogen than without. Partial defoliation in May had relatively little effect on yield. Defoliation affected the incidence of virus yellows differently in different years.     

The efficiency of visual assessment of grain yield and its components in spring barley rows

The efficiency of visual assessment for grain yield and its components in spring barley rows was examined using a number of assessors. In 20 out of 28 combinations of assessor and character, only 20 or less lines were needed to be retained from the set of 99 lines to save at least 50% of the best 10 lines. Assessments of tillers/row and to a lesser extent 1000-grain weight were generally more effective than assessments of yield/row and grain/ear. The low effectiveness of assessment of grains/ear was attributed to inadequate sampling of ears. Four out of five assessors showed bias towards assessment of tillers/row, the most easily assessed character, in their assessments of yield/row. Experienced barley workers were more successful in their assessments than others less familiar with the crop. Specially developed keys, aimed at making visual assessment more objective, generally had only small positive effects on the efficiency of assessment. Repeated assessments of characters by some assessors were consistent. It was concluded that visual assessment rather than direct measurement should be recognised as a basic tool of breeding in the early generations, using a large number of lines as a ‘safety net’ allowing the loss of some of the best lines.     

The effect of Drechslera teres seed infection on spring barley seedling growth

Barley seedlings (cv. Beatrice) emerging from seed infected with Drechslera teres were sorted into healthy seedlings, those with leaf sheath lesions and those with leaf blade lesions. Leaf area, plant height and total weight were reduced relative to healthy plants; leaf emergence also appeared to be delayed.     

The effects of yellowing viruses on yield of sugar beet in field trials, 1985 and 1987

The separate effects of beet yellows virus (BYV) and beet mild yellowing virus (BMYV) on yield of sugar-beet cultivars inoculated at different growth stages were assessed in field trials in 1985 and 1987. Early or mid-season inoculation decreased sugar yield by up to 47% for BYV, and up to 29% for BMYV. Infections after the end of July had no significant effect on yield. Both viruses caused significant increases in the juice impurities sodium, potassium and amino-nitrogen after infecting plants early in the season. Yield losses associated with infection were determined by the causative virus, the time of infection, and susceptibility of the sugar-beet cultivars.     

Colonization of the developing rhizosphere of sugar beet seedlings by potential biocontrol agents applied as seed treatments

AIMS: Poor colonization of the rhizosphere is a major constraint of seed treatment biological control. The objectives of this study were to; examine the colonization of the rhizosphere of sugar beet seedlings by selected rhizobacteria; determine the influence of the host rhizosphere and percolating water on the distribution of the bacteria; and deliver two biological control agents (BCAs) by co-inoculation. METHODS AND RESULTS: Rifampicin-resistant bacterial strains (Rif +) applied as single treatments to seed sown in columns of field soil produced persistent populations of 5-9 log10 cfu g-1 in the infection court of the damping-off pathogen Aphanomyces cochlioides in a controlled environment. However, isolates varied in their ability to colonize the lower rhizosphere. Percolating water significantly increased the colonization of the upper rhizosphere. Bacterial populations in the soil profiles of "non-rhizosphere" controls declined markedly with time. There was no interaction between the two selected BCAs applied as a seed treatment mixture. CONCLUSIONS: The distribution of the bacteria resulted primarily from root colonization although percolating water may modify the colonization profiles. Co-inoculation of the sugar-beet rhizosphere is a viable proposition. SIGNIFICANCE AND IMAPCT OF THE STUDY: Potential BCAs were successfully delivered to the known infection court of A. cochloides and persisted for the infection period. This bioassay can be used as a tool for the selection of BCAs for field trials.     

The effect of polyamines on the development of sugar beet protoplasts

The influence of the exogenous polyamines: putrescine, spermidine and spermine, on the frequency of protoplast divisions for 2 genotypes of sugar beet (Beta vulgaris L.) was analyzed. Protoplasts were cultured by the agarose disk method on Saunders and Doley medium supplemented with either hormones or polyamines, or hormones combined with polyamines. The latter supplement led to a statistically significant increase in plating efficiency. The improvement in division index was caused mainly by spermine. This revised version was published online in July 2006 with corrections to the Cover Date.     

The growth and development of the storage root of sugar beet

A study was made of the growth of the storage root of sugar beet as a sugar accumulating organ. The storage root grew by simultaneous cell multiplication and expansion from a series of peripheral secondary meristems laid down during the early stages of development. The weight of water and of non-sugar dry matter per cell increased in proportion to the increase in cell volume. The amount of sugar per cell was proportional to cell volume only during the initial stage of cell expansion up to volumes of about 15 times 10^-8 cm³; thereafter it was less proportional. Thus, average cell size is a major determinant of the sugar concentration of the storage root. The implications of this are discussed.     

Relationship between EUF-K contents,K uptake and sugar yield of sugar beet in deep loess soils

Summary In field experiments with varying K fertilization (1981 and 1982) changes in EUF-K contents were studied in deep loess soils of Southern Lower Saxony under sugar beet. A significant positive linear relationship was found between EUF-K contents at 20°C and 200 V (15 mA) of the topsoils and quantities of K absorbed by sugar beet in both years. The corresponding regression lines for 1981 and 1982 are almost parallel, the only difference being the yield level which was higher in 1982.The relationship between EUF-K contents at 20°C of topsoils and sugar yields showed the same parallelism for the two years. Not much increase in sugar yield was found at EUF-K contents over 12 mg/100 g soil at EUF-K 80°C/EUF-K 20°C ratios between 0.5 and 0.7. To attain a sugar yield of 10 t/ha an EUF-K 20°C value of at least 12 mg/100 g soil is required for these deep soils at the beginning of the K uptake period. This finding confirms experiences gained over an 8-year period at the Tulln Sugar Factory (Austria) with fertilizer recommendations based on EUF.     

The effect of transient and continuous drought on yield, photosynthesis and carbon isotope discrimination in sugar beet (Beta vulgaris L.)

Stable carbon isotope discrimination (delta13C), photosynthetic performance (A), dry matter accumulation (DW), and sucrose yield (Y(s)) of sugar beet were evaluated in a glasshouse experiment under transient (TS) and permanent (PS) water stress. A was significantly reduced under drought, to an extent depending on stress duration. The reduced A was strictly associated with a low DW and Y(s), the later being 42% lower in PS than control plants (C). Restoring water steeply increased A and the associated leaf traits (RWC, leaf water potential etc.), but the increase of Y(s) was negligible. Therefore, the negative effects of severe water stress in the early growth period, though reversible on gas-exchange and most leaf traits, can drastically reduce Y(s) of sugar beet. Furthermore, A seems not to be effective in predicting sucrose accumulation, although it was very effective in detecting the occurrence of plant water stress. The A/C(i) model was used to assess the photosynthetic adjustments to continuous or transient drought by calculating the photosynthetic parameters Vcmax and Jmax and then compared with delta13C. Mesophyll conductance (g(m)) was estimated by comparing delta13C measured on soluble sugars and gas-exchange data. This approach confirmed the expectation that g(m) was limiting A and that there was a significant drop in [CO2] from the substomatal cavities and the chloroplast stroma both in favourable and drought conditions. Therefore, the carbon concentration at the carboxylation site was overestimated by 25-35% by conventional gas-exchange measurements, and Vcmax was consistently underestimated when g(m) was not taken into account, especially under severe drought. Root delta13C was found to be strictly related to sucrose content (brix%), Y(s) and root dry weight, and this was especially clear when delta13C was measured on bulk dry matter. By contrast, leaf delta13C measured in soluble sugars (delta(s)) and bulk dry matter (delta(dm)) were found to correlate weakly to brix% and yield, and this was not surprising as the integration time-scale of leaf delta(s) and delta(dm) were found to be shorter than that of root delta13C in bulk dry matter. The effect of water stress on diffusive and biochemical limitations with different integration times ranged from 1 d (leaf delta(s)) to more than 1 month (root delta(dm)).     

Effects of soil density on yield and fertilizer requirement of sugar beet

Three experiments (1971–3) on medium-textured soils of low organic-matter content examined the effects of soil density on seedling emergence and yield of sugar beet, and the interactions between soil density and the requirement for nitrogen (N) and phosphate (P₂O₅) fertilizers. Three soil densities were produced by rolling and harrowing, dutch harrowing twice, and power harrowing once; each was tested with 75, 150 and 225 kg ha^-1 N and 0, 100 and 200 kg ha^-1 P₂O₅. Most seedlings emerged on the medium-density treatment produced by dutch harrowing twice. The crop in the least dense soil treatment, produced by power harrowing once, consistently yielded slightly more sugar than the medium-density treatment, which yielded significantly more than the most dense treatment. In dense soil, created by rolling and harrowing, there was a response to more fertilizer N than the less dense ones; the crop did not respond to phosphate fertilizer. Mechanical impedance, not toxic concentrations of ethylene in the soil atmosphere, appeared to be the cause of reduced yield on the dense soils; these reductions were considerable at dry soil bulk densities in excess of 1·5 g ml^-1.     

The effects of temperature on leaf growth of sugar beet varieties

Leaf growth of nine varieties of sugar beet (Beta vulgaris L.) was studied at constant temperatures of 7, 11, 15 and 20·C, using generalised logistic curves fitted to the data to estimate the parameters of growth. The rate of leaf appearance increased linearly with temperature and was the same in all varieties. There were differences between varieties in the weighted mean rates of expansion of leaf area per plant (ā), the temperature coefficient of ā and the leaf area duration (D); these differences were caused more by differences in rates of expansion and final sizes of individual leaves than by differences in rates of leaf production. The growth of the first six leaves produced by each plant was examined in detail. The greater size of successive leaves of plants and genotypic differences between comparable leaves were more attributable to differences in the rate than differences in the duration of leaf expansion. Increasing temperatures increased leaf size because they accelerated the rate of expansion more than they shortened the duration of the expansion phase. It is inferred that all effects arose through differences in the initial sizes of leaves before they unrolled from the shoot apex. Dry matter production was proportional to D but was partitioned more to the storage root at the colder temperatures. This may have been related to the differential effects of temperature on cell division and expansion and the relative contribution of these two processes to the final sizes of the leaves and storage root.