Tissue composition and arrangement in sugar beet genotypes of different tissue strength with regard to damage and pathogen infestation

2020 ◽  
pp. 114-123
Author(s):  
Nelia Nause ◽  
Tobias Meier ◽  
Christa M. Hoffmann

Drought stress affects yield formation and quality of sugar beet. The aim of this study was to identify the growing period, in which drought stress has the greatest impact on growth, and furthermore, to analyze the response of different sugar beet genotypes. Causes for a different response should be identified. In pot experiments in the greenhouse, drought stress was simulated by reducing irrigation to 60% of the water holding capacity (WHC) for four weeks at various growth stages followed by re-watering. Growth reduction was greatest when drought stress occurred early in the season: the content of the quality-determining non-sugars was highest, sugar yield and beet diameter were lowest. Responses of the genotypes in sugar yield, but primarily in the accumulation of osmotically active substances differed. Despite re-watering after drought stress the restrictions could not be compensated during growth. The transpiration coefficient of the drought-stressed treatments was only slightly different to the control, because water consumption in the control did not either increase at average air temperatures beyond 23 °C. The strong effect of early drought stress could be attributed to the high growth rates, so that a limited water supply affected yield formation more than at later growth stages. The storage losses of sugar beet genotypes are closely related to damage during harvest and subsequent infestation with mould and rots. Genetic variation for storability seems to be primarily linked to textural properties of the roots such as the resistance against mechanical damage. However, no information is available about the tissue strength, tissue composition and structural organization leading to an enhanced resistance against damage and pathogen attack. Therefore, the aims of the study were the identification of genotypic differences concerning tissue strength of the beet, the relation to damage and pathogen infestation and the underlying physiological basis of tissue strength. Field trials were carried out with 6 genotypes at 2 locations in 2018. The roots were harvested in August and November. After harvest in November, a storage trial was carried out. The root strength increased from August to November. Beets with a high puncture resistance of the periderm also had a firm inner tissue. Genotypic differences in puncture resistance were not affected by the harvest time, indicating that this trait is stable throughout the growing period. A higher puncture resistance of the beet was related to a lower mould growth during storage. Genotypes with varying tissue strength also differed in fiber content (AIR), but the composition of AIR was stable over genotypes. The number of cambium rings seems not to essentially influence the tissue strength of the beet. In the further course of the project, microscopic analyzes will clarify, whether genotypic differences in tissue strength can be attributed to cell size or cell wall thickness.

2020 ◽  
pp. 104-113
Author(s):  
Henning Ebmeyer ◽  
Christa M. Hoffmann

Drought stress affects yield formation and quality of sugar beet. The aim of this study was to identify the growing period, in which drought stress has the greatest impact on growth, and furthermore, to analyze the response of different sugar beet genotypes. Causes for a different response should be identified. In pot experiments in the greenhouse, drought stress was simulated by reducing irrigation to 60% of the water holding capacity (WHC) for four weeks at various growth stages followed by re-watering. Growth reduction was greatest when drought stress occurred early in the season: the content of the quality-determining non-sugars was highest, sugar yield and beet diameter were lowest. Responses of the genotypes in sugar yield, but primarily in the accumulation of osmotically active substances differed. Despite re-watering after drought stress the restrictions could not be compensated during growth. The transpiration coefficient of the drought-stressed treatments was only slightly different to the control, because water consumption in the control did not either increase at average air temperatures beyond 23 °C. The strong effect of early drought stress could be attributed to the high growth rates, so that a limited water supply affected yield formation more than at later growth stages.


Antioxidants ◽  
2021 ◽  
Vol 10 (3) ◽  
pp. 398
Author(s):  
Muneera D. F. AlKahtani ◽  
Yaser M. Hafez ◽  
Kotb Attia ◽  
Emadeldeen Rashwan ◽  
Latifa Al Husnain ◽  
...  

Drought stress deleteriously affects growth, development and productivity in plants. So, we examined the silicon effect (2 mmol) and proline (10 mmol) individually or the combination (Si + proline) in alleviating the harmful effect of drought on total phenolic compounds, reactive oxygen species (ROS), chlorophyll concentration and antioxidant enzymes as well as yield parameters of drought-stressed sugar beet plants during 2018/2019 and 2019/2020 seasons. Our findings indicated that the root diameter and length (cm), root and shoot fresh weights (g plant−1) as well as root and sugar yield significantly decreased in sugar beet plants under drought. Relative water content (RWC), nitrogen (N), phosphorus (P) and potassium (K) contents and chlorophyll (Chl) concentration considerably reduced in stressed sugar beet plants that compared with control in both seasons. Nonetheless, lipid peroxidation (MDA), electrolyte leakage (EL), hydrogen peroxide (H2O2) and superoxide (O2●−) considerably elevated as signals of drought. Drought-stressed sugar beet plants showed an increase in proline accumulation, total phenolic compounds and up-regulation of antioxidant enzymes catalase (CAT) and superoxide dismutase (SOD) activity to mitigate drought effects. Si and proline individually or the combination Si + proline considerably increased root and sugar yield, sucrose%, Chl concentration and RWC, MDA and EL were remarkably reduced. The treatments led to adjust proline and total phenolic compounds as well as CAT and SOD activity in stressed sugar beet plants. We concluded that application of Si + proline under drought stress led to improve the resistance of sugar beet by regulating of proline, antioxidant enzymes, phenolic compounds and improving RWC, Chl concentration and Nitrogen, Phosphorus and Potassium (NPK) contents as well as yield parameters.


Weed Science ◽  
2008 ◽  
Vol 56 (3) ◽  
pp. 457-463 ◽  
Author(s):  
Kalliopi Kadoglidou ◽  
Chrysovalantis Malkoyannidis ◽  
Kalliopi Radoglou ◽  
Ilias Eleftherohorinos ◽  
Helen-Isis A. Constantinidou

Field experiments were conducted in northern Greece during 2001 and repeated in 2002 and 2004 to evaluate the effects of pronamide on sugar beet. Total leaf area, leaf area index (LAI), leaf and root dry weights, photosynthetic yield (quantum yield of photochemical energy conversion in photosystem II), chlorotic index, and yield components of sugar beet were monitored after pronamide application. Three sugar beet cultivars, ‘Avantage’, ‘Dorothea’, and ‘Bianca’, requiring short, intermediate, and long vegetative periods, respectively, were subjected to treatment. Pronamide was applied on sugar beet either as a double application of 0.63 kg ai ha−1at the two- to four-leaf and 0.63 kg ai ha−1at the four- to six-leaf stage or as a single application of 1.26 kg ai ha−1performed at the latter leaf stage. Both application procedures were combined with a split application of phenmedipham at 0.04 kg ai ha−1plus desmedipham at 0.04 kg ai ha−1plus metamitron at 0.70 kg ai ha−1plus ethofumesate at 0.10 kg ai ha−1plus mineral oil at 0.50 L ha−1applied POST at the cotyledon–to–two-leaf as well as at the four-leaf growth stages. Pronamide (both single and double application) initially caused chlorosis and reduction of sugar beet growth. LAI and photosynthetic yield were also significantly affected for a 2-mo period following the final application, after which the negative effects caused by pronamide were ameliorated. At harvest, sugar beet root and sugar yield, sucrose, K+, Na+, and N-amino acid concentrations were not affected by the herbicide treatments compared with those produced in weed-free and herbicide-free plots, indicating that all cultivars managed to overcome the transient pronamide stress. Regarding sugar beet cultivars, root and sugar yield of Avantage and Dorothea at harvest were higher than that of Bianca, whereas sucrose concentration of Avantage was the lowest. There was not an apparent relationship between the order of sugar yield per cultivar (Dorothea > Avantage > Bianca) and the length of the vegetative period (Avantage < Dorothea < Bianca).


2020 ◽  
Vol 4 (2) ◽  
pp. 78-82
Author(s):  
Mohd Syahmi Salleh ◽  
Ris Amirah Malek ◽  
Rozilawati Shahari ◽  
Mohd Shukor Nordin

Drought is regarded as one of the limiting factors in rice production nationally and globally. The present study was conducted to study morpho-physiological and biochemical responses of rice genotypes to drought stress, to identify potential traits for use as a selection criterion in breeding drought-tolerant rice at seedling stage and finally to identify rice genotype resistant to drought stress for use as parents in future breeding. The experimental design used was a split-plot design with three replications, with drought stress as the main plot and rice genotypes as the sub-plot. The main plots consisted of control (normal irrigation) and drought stress. The sub-plots consisted of twelve rice genotypes namely Apami (V1), Boewani (V2), Basmati 370 (V3), Cica- 4 (V4), Dular (V5), Jarom mas (V6), Kalarata (V7), Biris (V8), Haiboq (V9), Moroberekan (V10), MR 297 (V11) and Aerob 1 (V12). Results showed that drought stress led to a decrease in plant height, leaves size, root length, total dry weight, and number of leaves but an increment in proline content. The genotype Apami and Kalarata were found to accumulate higher proline content indicating potential resistant ability towards drought stress. Dular and Aerob1, along with tolerant control genotype, Moroberekan, on the other hand, recorded a lower SES score. Leave size, root length, and plant height could also be used as a selection criterion in breeding drought-tolerant rice due to high values of broad-sense heritability and genetic advance by percentage of mean (GAM). Nevertheless, further study on the genetics and physiological basis of tolerant ability at reproductive growth stages are necessary in order to assess grain yield potential of the potentially tolerant genotype reported in this study.


2016 ◽  
Vol 42 (1) ◽  
pp. 127 ◽  
Author(s):  
V. Potopová ◽  
P. Štěpánek ◽  
A. Farda ◽  
L. Türkott ◽  
P. Zahradníček ◽  
...  

The study is focused on drought stress that is detrimental to yield formation of field-grown vegetables in the lowland regions of the Czech Republic. Extensive vegetable yield losses are attributed to drought, often in combination with heat or other stresses. The objective of this research was to investigate, under field conditions, the effect of drought stress quantified by the Standardized Precipitation Evapotranspiration Index (SPEI) on yield variability of key vegetable crops growing in the Elbe River lowland, representing central European agriculture conditions. Additionally, we also tried to determine the period of crop with the highest sensitivity to drought (PCSD) of vegetable crops over the Elbe River lowland. Historical climate datasets for a regular gridded network with a high horizontal resolution of 10 km (CZGRIDS) and 305 climatological stations from the Czech Hydrometeorological Institute were applied. The SPEI at 1-, 3-, and 6-month lags was calculated for the period 1961-2014 based on precipitation and input dataset for the reference evapotranspiration (ETr) by the Penman-Monteith (PM) method. Moreover, the difference between daily precipitation and crop evapotranspiration (ETc) has been used to calculate the mean crop water balance (D) per main growth stages, as an indicator of plant stress. This improvement increased the applicability of the SPEI in agriculture drought impact on rainfed and/or irrigated field crops grown under various agronomic management systems. To understand how the SPEI, over the period 1989-2014, controlled the yield variation, we calculated the percentage of yield losses and gains for each crop. When the value of SPEI at 3-month lag–as a measure of the balance between the water availability and the atmospheric water demand–for PCSD was between -1.49 and 0.99, the yield moderately increased for Fruiting vegetables (e.g. tomatoes, cucumber). Conversely, when the SPEI-3 in the key development stage dropped below -3.0, the yield losses were about -30% and a negative influence is apparent from threshold of the SPEI≤-1.5. The effect of the SPEI on yield formation of vegetable cultivars grown under filed conditions was achieved up to 62% in the study region.


1970 ◽  
Vol 75 (2) ◽  
pp. 223-229 ◽  
Author(s):  
R. Hull ◽  
D. J. Webb

SUMMARYA field experiment in each year 1963 to 1967 in Suffolk, England, tested the effect on yield of sugar beet of sowing dates ranging from 13 March to 11 May and harvest dates ranging from 20 September to 8 December. Sowings in March or early April gave similar yields of sugar but with later sowings yield decreased progressively faster. The relationship is represented by the equationy = 106·3 (±2·24) + 0·212 (±0·184)x-0·009 (±0·003)x2,y = yield as percentage of mean (60·1 cwt/acre of sugar), x = number of days after 12 March.Delayed harvest increased sugar yield; the relationship is represented by the equationy = 80·22 (±1·51) + 0·836 (±0·09)z-0·006 (±0·001)z2,z = number of days after 19 September. This represents an increase of 0·247 cwt/acre/day of sugar in October and 0·083 cwt/acre/day in November, equivalent to about 2½ tons/acre of roots in October and 1 ton/acre in November.The effect on sugar yield of different lengths of growing period, which ranged from 138 to 271 days, is represented by the equationy = 38·7 (±26·6) + 1·045 (±0·267)a-0·0017 (±0·0007)a2,a = number of days between sowing and harvest.On average, sowing date had negligible effect on sugar percentage at harvest. In 3 years sugar percentage increased after the first harvest to a maximum and then decreased; in 2 years it decreased with consecutive harvests.


1973 ◽  
Vol 81 (2) ◽  
pp. 267-275 ◽  
Author(s):  
A. P. Draycott ◽  
D. J. Webb ◽  
E. M. Wright

SummaryFour field experiments (1968–71) investigated the effect of changing the length of the growing period on the nitrogen fertilizer requirement of sugar beet. The crop was sown on three occasions (March–May), harvested on three occasions (September–December) and given four amounts of fertilizer (0–225 kg N/ha). Plant samples were analysed at several stages of growth (1969–71) in an attempt to predict the amount of nitrogen fertilizer needed for maximum sugar yield and also at the end of the season to determine the nitrogen uptake. Increasing the length of the growing period increased sugar yield greatly but the amount of nitrogen fertilizer needed for maximum sugar yield was unchanged. The crop given the largest dressing of nitrogen and with the longest growing period contained most total nitrogen, but in every experiment, giving more than 75 kg N/ha neither increased nor decreased the sugar yield significantly. As a result of the small variations in nitrogen requirement, the plant analyses during the growing season were of little value in predicting the needs of the crop.


1971 ◽  
Vol 77 (1) ◽  
pp. 61-68 ◽  
Author(s):  
M. J. Durrant ◽  
A. P. Draycott

SummaryTen experiments (1967–9) on sandy soil in East Anglia measured the effect of magnesium fertilizer on yield and cations in sugar beet. Magnesium fertilizer increased sugar yield by up to 0·80 t/ha and on the three most responsive fields it consistently increased top and root dry·matter yields throughout the growing period.On average, without magnesium fertilizer, the concentration of magnesium in tops progressively decreased from 0·33% at singling to 0·15% at harvest, and in roots from 0·39% to 0·09%. The corresponding decreases with magnesium fertilizer were (tops) from 0·68% to 0·20% and (roots) from 0·48% to 0·10%. Yield was increased by magnesium fertilizers when tops contained less than 0·35% Mg during May, 0·30% during June, 0·22% during July and 0·17% during August. Deficiency symptoms were not visible until the concentration in tops averaged less than 0·2% – the percentage of plants with symptoms increased rapidly at smaller concentrations. Magnesium fertilizer decreased the concentration of calcium in tops and roots but did not affect the concentration of potassium or sodium.The maximum amount of magnesium, potassium, sodium and calcium in tops (August–September) was 11, 218, 75 and 62 kg/ha respectively; these decreased to 8, 168, 55 and 50 kg/ha at harvesting, showing that only about 75% of the largest amount in tops was present at harvest. The amounts removed in roots at harvest were 9 kg/ha Mg, 75 kg/ha K, 11 kg/ha Na and 26 kg/ha Ca. A dressing of 100 kg/ha magnesium increased the amount of magnesium in the crop at harvest by only 4·5 kg/ha.


2015 ◽  
Vol 202 (6) ◽  
pp. 530-541 ◽  
Author(s):  
K. Schnepel ◽  
C. M. Hoffmann

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