Legume Research

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Legume Research, volume 47 issue 3 (march 2024) : 435-440

​Effect of High Minimum Temperature and Enriched Night CO2 on Yield and Seed Quality of Black Gram (Vigna mungo) under Soil Plant Atmospheric Research (SPAR)

M. Guna1,*, S.P. Ramanathan1, V. Geethalakshmi1, K. Chandrakumar1, S. Kokilavani1, M. Djanaguiraman1
1Agricultural College and Research Institute, Tamil Nadu Agricultural University, Coimbatore-641 003, Tamil Nadu, India.

  • Submitted23-06-2022|

  • Accepted23-08-2022|

  • First Online 02-09-2022|

  • doi 10.18805/LR-4989

Cite article:- Guna M., Ramanathan S.P., Geethalakshmi V., Chandrakumar K., Kokilavani S., Djanaguiraman M. (2024). ​Effect of High Minimum Temperature and Enriched Night CO2 on Yield and Seed Quality of Black Gram (Vigna mungo) under Soil Plant Atmospheric Research (SPAR) . Legume Research. 47(3): 435-440. doi: 10.18805/LR-4989.

ABSTRACT

Background: Black gram is a leguminous plant species. This pulse crop has been grown on the Indian subcontinent for a long time. Black gram a drought-resistant crop that grown both in the summer and the winter, usually in rotation with rice but occasionally in mixed farming. The objective of this research was to (i) quantify the short-term effects of high minimum temperature and enriched night CO2 (HMT and enCO2) on yield contribution factors and (ii) quantify seed quality parameters employing biochemical analysis. 

Methods: An investigation was carried out during summer 2021 and 2022 to evaluate the effect of high minimum temperature (ambient+3°C) and enriched night CO2 (600 ppm) (HMT and enCO2) on yield and seed quality parameters of black gram (Vigna mungo) under soil plant atmospheric research (SPAR) and ambient condition at Agro Climate Research Centre, Tamil Nadu Agricultural University, Coimbatore, Tamil Nadu with ten treatments which were replicated thrice.

Result: Black gram yield and quality parameters were significantly (p=0.05) reduced under HMT and enCO2. Pooled data from two successive summer seasons revealed that stress from (i) 50 to 56 DAS (Days after sowing), the number of flowers dropped per plant significantly increased by 24% and pod setting percent decreased by 19.9% (ii) 43 to 49 DAS, grain yield and biomass/plant decreased by 25.4% and 16.2%, respectively. Seed quality parameters revealed that stress during 50 to 56 DAS, seed protein, total sugar content, polyphenols, calcium and iron decreased by 19.4%, 23.7%, 16.2%, 29.6% and 30.2%, respectively. The proline and phytic acid were statistically reduced by 53.9% and 59.1%, respectively stress during 50 to 56 DAS. Stress from 64 to 70 DAS, seed moisture content was significantly decreased by 32.1%. Overall, black gram yield and seed quality was negatively affected on two treatments: stress imposed from 43 to 49 DAS (T7) and stress imposed from 50 to 56 DAS (T8) (50% flowering to pod filling stage).

INTRODUCTION

Pulses are major food crops that can help address future global food security and widely cultivated in the semi-arid tropics as a source for nutritional protein, feed and fodder. Black gram is a significant legume crop with high protein and mineral content (FAO, 2021). Variability and change in climatic parameters, such as temperatures, rainfall and changes in atmospheric carbon dioxide concentrations as a result of global warming, have a significant impact on the agricultural production system. Many research on crops reveals that the negative effects of climate change on crop yields have been more common than the positive effects at the global level. Carbon dioxide (CO2) concentrations in the atmosphere have risen from 280 parts per million (ppm) before the industrial revolution to 418.7 parts per million (ppm) today. CO2 is increasing at a rate of 3 ppm per every year and is anticipated to reach 750 parts per million by the end of the twenty-first century (WMO, 2021). The diurnal variation of global CO2 concentration revealed that it is higher at night than during the day due to natural activities (Metya et al., 2021). Rapid rises in minimum night temperatures compared to maximum day temperatures are expected in the future, causing significant crop productivity. Between 1970 and 2019, India’s minimum temperature increased at a higher rate than its maximum temperature (Ray et al., 2019). Major crops like rice, wheat, sorghum and legumes that are vulnerable to high minimum temperature stress (HMT) (Impa et al., 2020). Physiological systems affected by HMT, include carbon balance, source-sink metabolite changes and reactive oxygen species. The effects of HMT on legume grain developmental dynamics are reviewed, with a focus on grain-filling length, post-flowering senescence, changes in grain starch, protein composition and starch metabolism enzymes (Garcia et al., 2018). A minimum temperature of above 24°C was identified as the key threshold beyond which yields and quality began to decline consistently in wheat (Garcia et al., 2016). However, under HMT and enCO2 in black gram, are still not clearly understood and need attention. In this contest, the role of high minimum temperatures on black gram needs to be understood. Specifically, we aim to study the short episodes of HMT and enCO2 on yield and seed quality parameters in black gram.

MATERIALS AND METHODS

To evaluate the impact of HMT and enCO2 on yield and seed quality characteristics of variety of black gram CO6, a pot culture experiment was done at SPAR (Soil Plant Atmospheric Research) unit, Agro Climate Research Centre, Tamil Nadu Agricultural University, Coimbatore (11.013251o - N, 76.939725° - E) during the summer season (March to May) 2021 and 2022. The two years (2021 and 2022), daily weather data with respect to maximum and minimum temperature (°C), average relative humidity (%) and rainfall (mm) prevailed during the summer season from March to May 2022 were collected from SPAR automatic data logger and Agro Climate Research Centre, Tamil Nadu Agricultural University, Coimbatore (Fig 1). Three replications were used in the CRD (Completely Randomized Design) experiment. A high yielding black gram culture CO6 (COBG 653) is a cross derivative of DU 2 × VB 20 and matures in 65-70 days. This culture recorded an average yield of 877 Kg/ha and found to be susceptible to yellow mosaic disease. The SPAR system contains a plexiglass chamber 2 × 1.5 metres in cross section and 2.5 metres height where crop is being grown. It also contains an air conditioner, as well as other required devices like a humidifier and dehumidifier, installed on a sturdy steel frame made of plexiglass with a 6 mm thickness. The software, named EMCON (environment control), was used to stimulate the required and accurate levels of temperature and CO2 inside the SPAR unit. The CO2 gas was supplied to the unit to maintain CO2 concentration at 600 ppm and an air conditioner was used to maintain the temperature levels at ambient +3oC during the night time (1800 to 0600 hrs IST), also plants were kept under ambient condition during the day time. The pot culture was maintained with well-watered condition and the pot culture was treated with RDF (Recommended dose of fetilizer) (25 kg N + 50 kg P2O5 + 25kg K2O + 40 kg S)/ ha and appropriate measurements were taken for pest and disease management during the crop season (TNAU crop production guide 2021).

Fig 1: Two years (2021 and 2022), average daily weather prevailed during March to May.



Stress: Ambient+3oC and 600 ppm CO2 (HMT and enCO2) during the night time. Experiment is designed with 10 treatments viz., T1: Control, T2: stress imposed from 7 to 14 DAS (Day After Sowing), T3: stress imposed from 15 to 21 DAS, T4: stress imposed from 22 to 28 DAS, T5: stress imposed from 29 to 35 DAS, T6: stress imposed from 36 to 42 DAS, T7: stress imposed from 43 to 49 DAS, T8: stress imposed from 50 to 56 DAS, T9: stress imposed from 57 to 63 DAS, T10: stress imposed from 64 to 70 DAS.
       
The yield attributes viz., number of flowers dropped/plant, Pod setting percent, Grain yield/plant and biomass/plant were recorded after the harvesting of the crop. The seed quality parameters viz., total sugars, protein, polyphenols, seed moisture, proline, phytic acid, calcium and iron were measured by standard methods. The powdered black gram grains (100 mg) were kept overnight in 25 ml of 0.1 N NaOH to extract total proteins and total proteins were quantified using the supernatant after centrifugation at 3000 rpm (5000xg) (Lowry et al., 1951).  80% ethanol was employed to extract free sugars from black gram powder, followed by 70% ethanol (Kaur et al., 2000). Total soluble sugars were determined from the pooled extract (Dubois et al., 1956). By refluxing dried seed powder with 80% aqueous methanol, the phenolic components were extracted. After filtering, total phenols were estimated using the refluxed sample (Swain and Hills, 1959). The AOAC method (2000) has been used to determine the seed moisture content of the samples. Proline was measured using the acid ninhydrin procedure and the absorbance was obtained spectrophotometrically at 520 nm after homogenization in 10 mL of 3% (w/v) sulfosalicylic acid Bates et al., (1973). The phytic acid was extracted from the powdered seeds with 1.2% HCl and precipitated with 0.4% ferric chloride (Zemel and Shelef, 1982). The Rouser et al., (1974) technique, which involved treating the sample with strong HCl and perchloric acid, has been used to determine the sample’s organic phosphorus level. In a muffle furnace, total ash was determined by burning and weighing a sample and the mineral content was calculated after it was dissolved in water. Using Wong’s Method, iron was identified colorimetrically (Raghuramulu et al., 2003). Calcium oxalate was precipitated, diluted in hot dilute H2SO4 and titrated against a potassium permanganate standard (Helrich, 1990).
       
SPSS 16.0 was used to perform statistical analysis on the data (SPSS Inc., Chicago, IL). For all data, the mean and standard deviation were determined and as suggested by Gomez and Gomez (1984), significant differences between mean values were evaluated using the Least Significant Difference (LSD) at a 5% probability level.

RESULTS AND DISCUSSION

Yield and yield attributes
 
Number of flowers dropped per plant ranged from 32.5 to 40.3 (Table 1). The lowest flower drop per plant (32.5) was recorded in black gram plants grown under ambient condition (T1), which was statistically on par with stress imposed from 7 to 14 DAS (T2) (33.9). This differed statistically from stress imposed during 50 to 56 DAS (T8) (40.3) which was on par with stress imposed from 43 to 49 DAS (T7) (40). This present study corroborates with Prasad et al., (2008) and Bahuguna et al., (2017), they reported that the peak flowering stage of the rice was most sensitive to high night temperature and reduced the overall number of flowers per plant.

Table 1: Effect of HMT and enCO2 on number of flowers dropped, pod setting percentage (%), yield (g/plant), total biomass (g/plant) of black gram (two years data pooled).


       
The data analysis shows that the HMT and en CO2 had significant (p = 0.05) influence on the pod setting per cent of black gram (Table 1). The highest pod setting per cent of black gram was recorded under ambient condition (T1) (57.1%) which was lower under stress imposed from 50 to 56 DAS (T8) (47.7%). This current study was in conformity with findings of Shi et al., (2017), which reported that the 8% reduction was measured at grain filling percent in rice crop under high minimum temperature. 
       
From the Table 1, the grain yield per plant was highest under stress imposed from 7 to 14 DAS (T2) (13.8 g/plant) followed by ambient condition (T1) and stress imposed from 15 to 21 DAS (T3) (13.4 g/plant). There was a significant reduction in the grain yield with stress imposed from 43 to 49 DAS (T7) and stress imposed from 57 to 63 DAS (T9) (10 g/plant) which on par with stress imposed from 50 to 56 DAS (T8) (10.2 g/plant). The current findings are consistent with the results of Hein et al., (2019), who reported that field-based heat tents experiment shows stress imposed from 50 percent flowering to maturity on wheat will reduce grain yield by 7 to 14%.
       
When compared to stress imposed from 7 to 14 DAS (17.6 g/plant), HMT and enCO2 significantly reduced the total biomass (14.4 g/plant) when stress imposed from 43 to 49 DAS (T7) followed by stress imposed from 50 to 56 DAS (T8) (14.7 g/plant) and stress imposed from 36 to 42 DAS (T6) (14.8 g/plant) (Table 1). This result correlated with the findings of Impa et al., (2020), who reported that increasing the high night temperature during anthesis and maturity stage would reduce the above ground biomass by 2 to 46% in wheat.

Nutritional and anti-nutritional compositions
 
The black gram plants that were grown in the ambient condition (T1) recorded high seed protein content (21.6%) on par with stress imposed from 7 to 14 DAS (T2) (21.2%) and was significantly (p=0.05) different from stress imposed from 50 to 56 DAS (T8) (17.4%). This was statistically on par with stress imposed from 43 to 49 DAS (T7) (17.7%) and stress imposed from 57 to 63 DAS (T8) (18.1%) (Table 2). Also, according to Impa et al., (2019), the seed protein of wheat crop was sensitive to high night temperature and illustrated 21% reduction of protein content in wheat.
       
Total sugar content (492.3 mg/g) was higher in black gram seed grown under stress imposed from 7 to 14 DAS (T2), which was statistically on par with ambient condition (T1) (491.3 mg/g). A significant difference was observed stress during 50 to 56 DAS (T8) (375 mg/g), which was on par with stress imposed from 36 to 42 DAS (T6) (377.8 mg/g) and stress imposed from 43 to 49 DAS (T7) (378.2 mg/g) (Table 2). According to Gogoi et al., (2018) total sugar content of groundnut seed was reduced by 24.5% under heat stress.

Table 2: Effect of HMT and enCO2 on seed protein (%), total Sugars (mg/g), polyphenols (mg/g) and seed moisture (%) of black gram (two years pooled data).


       
The total polyphenols content (7.4 mg/g) was significantly higher in black gram seeds grown under ambient condition (T1) which was statistically on par with stress imposed from 15 to 21 DAS (T3) (7.3 mg/g) and stress imposed from 7 to 14 DAS (T2) (7.2 mg/g) and lower polyphenol was recorded in stress imposed from 50 to 56 DAS (T8) (6.2 mg/g) (Table 2). Total polyphenols help to overcome various stresses like heat and cold stress (Kaushal et al., 2016). Singh et al., 2015, reported that the flowering to pod development stage of legume crops would be affected by the high temperature stress.
       
The level of seed moisture as influenced by the HMT and enCO2 are given in Table 2. The range varies from 8 to 11.9% among the treatments. The stress imposed from 64 to 70 DAS (T10) had the lowest moisture content (8%), followed by stress imposed from 57 to 63 DAS (T9) and stress imposed from 50 to 56 DAS (T8) (8.4%) whereas the highest seed moisture content (11.9%) was recorded under stress imposed from 7 to 14 DAS (T2). Based on the research findings of Sehgal et al., 2018, the heat stress on pulse crops reduced the seed moisture content under the maturity stage than the other stages. In the present study, lower seed moisture content was observed during the maturity stage of the crop.
       
Significantly (p = 0.05) lower proline content (39.9 mg/g) was recorded under ambient condition (T1) which was statistically on par with stress imposed from 15 to 21 DAS (T3) (40.5 mg/g). The highest proline content (61.4 mg/g) was found in stress imposed from 50 to 56 DAS (T8) followed by stress imposed from 43 to 49 DAS (T7) (59 mg/g) (Table 3). Similar to present studies Liu et al., 2019 found that increased proline content by 40% in bean seeds.

Table 3: Effect of HMT and enCO2 on proline (mg/g), phytic acid (mg/g), calcium (mg/100g) and iron (mg/100g) of black gram (two years pooled data).


       
The phytic acid content was found significantly lower (8.3 mg/g) under stress imposed from 15 to 21 DAS (T3) followed by stress imposed from 7 to 14 DAS (T2) (8.6 mg/g) and ambient condition (T1) (8.8 mg/g). Higher phytic content was recorded in stress imposed from 50 to 56 DAS (T8) (14 mg/g) which was on par with stress imposed from 43 to 49 DAS (T7) (12.8 mg/g) (Table 3). Temperature stress on pulse crops during reproductive stages increases phytic acid, which leads to malnutrition, according to Gillman et al., 2021. The essential minerals like calcium, iron and zinc were known to be absorbed by phytic acid. As a result, increasing the high minimum temperature in the black gram seeds will increase the phytic acid content. Choukri et al., 2022 findings reveal that 14% phytic acid content had increased during the reproductive stage in lentils.
       
Significantly (p = 0.05) higher calcium content (239 mg/100 g) was recorded under stress imposed from 7 to 14 DAS (T2) which was on par with ambient condition (T1) (238 mg/100 g). Comparatively, lower calcium content (168 mg/100g) was found when stress imposed from 50 to 56 DAS (T8) followed by stress imposed from 43 to 49 DAS (T7) (175 mg/100 g) (Table 3). The present study corroborates the results of Farooq et al., 2018, also found that decreased calcium content in legume crops under the high night temperature on the pod filling stage.
               
Higher iron content of black gram (34.3 mg/100 g) was recorded in stress imposed from 7 to 14 DAS (T2) which was on par with stress imposed from 15 to 21 DAS (T3) (34 mg/100 g) and ambient condition (T1) (33.1 mg/100 g) and statistically differed with stress imposed from 50 to 56 DAS (T8) (23.1 mg/100g) followed by stress imposed from 43 to 49 DAS (T7) (24.1 mg/100 g) due to HMT and enCO2 (Table 3). The current investigation supports the findings of Sarkar et al., (2021), who assessed decreased iron content in legume crops under temperature and CO2 stress during the pod filling stage. 

CONCLUSION

Increase in minimum temperature could have greater global effect due to its persistence over long periods during crop cycle, possibly affecting a wide range of growth and development stages. According to the findings of this study, HMT and enCO2 have an adverse effect on black gram production and seed quality. However, there was only a minimal effect observed on black gram from emergence to vegetative phase (stress from 7 to 28 days after sowing). As a result, high minimum temperature and enriched night CO2 will have a negative impact on food security in the future.

CONFLICT OF INTEREST

All authors declared that there is no conflict of interest.

REFERENCES


  1. AOAC. (2000). Official Methods of Analysis, 17th edition. Association of Official Analytical Chemists, Arlington.

  2. Bahuguna, R.N., Solis, C.A., Shi, W., Jagadish, S.V.K. (2017). Post flowering night respiration and altered sink activity account for high night temperature-induced grain yield and quality loss in rice (Oryza sativa L.). Physiologia Plantarum. 159: 59-73.

  3. Bates, L.S., Waldren, R.P., Teare, I.D. (1973). Rapid determination of free proline for water stress studies. Plant Soil. 39: 205-207.

  4. Choukri, H., El Haddad, N., Aloui, K., Hejjaoui, K., El-Baouchi, A., Smouni, A., Kumar, S. (2022). Effect of high temperature stress during the reproductive stage on grain yield and nutritional quality of lentil (Lens culinaris Medikus). Frontiers in Nutrition. 9. https://doi.org/10.3389/fnut.2022.857469

  5. Dubois, M., Gills, K.N., Hamilton, J.K., Robers, P.A., Smith, F. (1956). Colorimetric method for the determination of sugars and related substances. Annals of Chemistry. 28, 350-356.

  6. FAO. (2021). World Food and Agriculture - Statistical Yearbook 2020. https://doi.org/10.4060/cb1329en.

  7. Farooq, M., Hussain, M., Usman, M., Farooq, S., Alghamdi, S.S., Siddique, K.H. (2018). Impact of abiotic stresses on grain composition and quality in food legumes. Journal of Agricultural and Food Chemistry. 66(34): 8887-8897.

  8. Garcia, G.A., Miralles, D.J., Serrago, R.A., Alzueta, I., Huth, N., Dreccer, M.F. (2018). Warm nights in the argentine pampas: Modelling its impact on wheat and barley shows yield reductions. Agricultural Systems. 162: 259-268.

  9. Garcia, G.A., Serrago, R.A., Dreccer, M.F., Miralles, D.J. (2016). Postanthesis warm nights reduce grain weight in field- grown wheat and barley. Field Crops Research. 195: 50-69.

  10. Gillman, J.D., Chebrolu, K., Smith, J.R. (2021). Quantitative trait locus mapping for resistance to heatinduced seed degradation and low seed phytic acid in soybean. Crop Science. 61(3): 2023-2035.

  11. Gogoi, N., Farooq, M., Barthakur, S., Baroowa, B., Paul, S., Bharadwaj, N. Ramanjulu, S., (2018). Thermal stress impacts on reproductive development and grain yield in grain legumes. Journal of Plant Biology. 61(5): 265-291.

  12. Gomez, K.A. and Gomez, A.A. (1984). Statistical Procedures for Agricultural Research (2 ed.). John Wiley and Sons, New York, 680p.

  13. Hein, N.T., Wagner, D., Bheemanahalli, R., Sebela, D., Bustamante, C., Chiluwal, A., Jagadish, S.V.K. (2019). Integrating field-based heat tents and cyber-physical system technology to phenotype high night-time temperature impact on winter wheat. Plant Methods. 15: 41. https://doi.org/10.1186/s13007-019-0424-x.

  14. Helrich, K. (1990). Official Methods of Analysis, 15th edition. Association of Official Analytical Chemists, Virginia.

  15. Impa, S.M., Sunoj, V.J., Krassovskaya, I., Bheemanahalli, R., Obata, T., Jagadish, S.K. (2019). Carbon balance and source- sink metabolic changes in winter wheat exposed to high night-time temperature. Plant, Cell and Environment. 42(4): 1233-1246. 

  16. Impa, S.M., Vennapusa, A.R., Bheemanahalli, R., Sebela, D., Boyle, D.,Walia, H., Jagadish, S.V.K. (2020). High night temperature induced changes in grain starch metabolism alters starch, protein and lipid accumulation in winter wheat. Plant, Cell and Environment. 43: 431-447.

  17. Kaur, S., Gupta, A.K., Kaur, N. (2000). Effect of GA3, kinetin and indole acetic acid on carbohydrate metabolism in chickpea seedlings germinating under water stress. Plant Growth Regulation. 30: 61-70.

  18. Kaushal, M. and Wani, S.P. (2016). Rhizobacterial-plant interactions: Strategies ensuring plant growth promotion under drought and salinity stress. Agriculture, Ecosystems and Environment.  231, 68-78.

  19. Liu, Y., Li, J., Zhu, Y., Jones, A., Rose, R.J., Song, Y. (2019). Heat stress in legume seed setting: Effects, causes and future prospects. Frontiers in Plant Science. 10: 938.

  20. Lowry, O.H., Rosebrough, N.T., Farr, A.L., Randall, R.J. (1951). Protein measurement with folin phenol reagent. Journal of Biological Chemistry. 193: 265-275.

  21. Metya, A., Datye, A., Chakraborty, S., Tiwari, Y.K., Sarma, D., Bora, A., Gogoi, N. (2021). Diurnal and seasonal variability of CO2 and CH4 concentration in a semi-urban environment of western India. Scientific Reports. 11(1): 1-13.

  22. Prasad, P.V.V., Pispati, S.R., Ristic, Z., Bukovnik, U., Fritz, A.K. (2008). Impact of night time temperature on physiology and growth of spring wheat. Crop Science. 48, 2372-2380.

  23. Raghuramulu, N., Nair, M.K., Kalyansundaram, S. (2003). A Manual of Laboratory techniques. National Institute of Nutrition, ICMR, Jamai Osmania, Hyderabad.

  24. Ray, L.K., Goel, N.K. Arora, M. (2019). Trend analysis and change point detection of temperature over parts of India. Theoretical and Applied Climatology. 138(1): 153-167.

  25. Rouser, G., Fleisher, S., Yamamoto, A. (1974). Two-dimensional thin layer chromatographic separation of polar lipids and determination of phospholipids by phosphorus analysis of spots. Lipids. 5: 494-496.

  26. Sarkar, S., Khatun, M., Era, F.M., Islam, A.M., Anwar, M.P., Danish, S., Islam, A.A. (2021). Abiotic stresses: Alteration of composition and grain quality in food legumes. Agronomy. 11(11): 2238.

  27. Sehgal, A., Sita, K., Siddique, K.H., Kumar, R., Bhogireddy, S., Varshney, R.K., Rao, B.H., Nair, R.M., Prasad, P.V. Nayyar, H., (2018). Drought or/and heat-stress effects on seed filling in food crops: impacts on functional biochemistry, seed yields and nutritional quality. Frontiers in Plant Science. 9: 1705.

  28. Shi, W., Yin, X., Struik, P.C., Solis, C., Xie, F., Schmidt, R.C., Jagadish, S.V.K. (2017). High day-and night-time temperatures affect grain growth dynamics in contrasting rice genotypes. Journal of Experimental Botany. 68: 5233-5245.

  29. Singh, A., Kumar, P., Sharma, M., Tuli, R., Dhaliwal, H.S., Chaudhury, A., Roy, J. (2015). Expression patterns of genes involved in starch biosynthesis during seed development in bread wheat (Triticum aestivum). Molecular Breeding. 35: 184.

  30. Swain, T. and Hills, E. (1959). The phenolic constituents of Prunus domestica. The quantitative analysis of phenolic constituents. Journal of the Science of Food and Agriculture. 10: 63- 68.

  31. WMO. (2021). State of Climate in 2021: Extreme events and major impacts.

  32. Zemel, M.B. and Shelef, L.A. (1982). Phytic acid hydrolysis with soluble zinc and iron in whole wheat bread as affected by calcium containing additives. Journal of Food Science. 47: 535-537.
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