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Effect of High Temperature on Rice 
Growth, Yield & Grain Quality 
By 
MEDIDA SUNIL KUMAR
Climate Change & Rice 
• Rice is a globally important cereal crop and as a primary source of food accounts 
for 35-75% of calories intake of more than 3 billion humans. 
• Climate change will cause tremendous damage to rice production sector if not 
addressed properly. Low rice supply along with increasing demand not only 
affects food security but also the economy of the country. 
• Reduce rice production in a sizable portion 
• Drought affects all stages of rice growth and development. The strong effects of 
drought on grain yield are largely due to the reduction of spikelet fertility and 
panicle exertion. 
• Climate change may also affect weed ecology, the evolution of weed species 
over time, and the competitiveness of C3 vs C4 weed species.
Cardinal Temperatures of rice 
• Critical low temperature -15oC 
• Optimum Temperature -20-30oC 
• Critical high temperature - 45oC
Role of Temperature on Growth & Development
Table: Effect of temperature on germination percentage 
Temperature Period Germination percent 
0-5o C >30 days 90 
25o C 6 days 90 
31-36 o C 2 days 90
Seedling growth 
• Growth rate linearly increases between 22 & 31OC 
• Temperatures of of 22oC or below are considered 
subnormal for seedling growth. 
• Seedling growth may be reasonably good up to 35oC, 
above which declines sharply. 
• Seedlings will die above 40oC. 
• Optimum temperature for cell division of the radicle is 
25oC and cell enlargement is 30oC. 
• Elongation of radicle stops below 15oC and above 40oC
Leaf emergence 
• Temperature is a principle environmental determinant of 
leaf appearance in rice. 
• As per the temperature summation index the 
development of one leaf requires about 100 degree days 
before initiation of panicle primordia.
Tillering 
• High temperature increases tillers 
• At 3-5 weeks after sowing temperature only 
slightly affected the tillering rate and RGR except 
lowest temperatures (Below 22oC). 
• Higher temperatures may effect the synchronism 
and in the mobilization of assimilates and 
nutrients among he tillers
• The optimum temperature for the normal development of 
rice ranges from 27 to 32 °C. 
• A temperature increase of 1 °C shortened the number of 
days from sowing to heading by 4–5 days for some 
genotypes (Nakagawa et al 2001). 
 Flowering and to a lesser extent the preceding stage 
booting are considered to be the stages of development 
most susceptible to temperature in rice (Satake & 
Yoshida 1978; Farrell et al. 2006)
HIGH TEMPERATURE AND SPIKELET STERILITY 
• Temperatures higher than the optimum induced floret sterility and thus decreased rice 
yield (Nakagawa et al. 2003). Spikelet sterility was greatly increased at temperatures 
higher than 35 °C (Matsui et al 1997). 
• In greenhouse experiments with both indica and japonica genotypes, Jagadish et al (2007) 
found that less than 1 h of exposure to temperatures above 33·7 °C was sufficient to 
induce sterility. 
• Enhanced O2 levels may further aggravate this problem, possibly because of reduced 
transpirational cooling (Matsui et al 1997a). 
• Exposure to 41 °C for 4 h at flowering caused irreversible damage and plants became 
completely sterile (IRRI 1976) whereas this high temperature (41 °C) had no effect on 
spikelet fertility at 1 day before or after flowering (Yoshida et al 1981). 
• There is genotypic variation in spikelet sterility at high temperature in both the sub-species 
of O. sativa, indica and japonica (Matsui et al. 2001; Prasad et al. 2006), which 
can be defined by different temperature thresholds (Nakagawa et al 2003). 
• However, in general, indica is more tolerant to higher temperatures than japonica (Satake 
& Yoshida 1978).
Mechanism of heat-induced floret sterility 
• Male reproductive system in rice is known to be more sensitive to heat 
stress (Wassmann et al. 2009a). Prasad et al. (2006) reported that high 
temperature stress during rice flowering led to decreased pollen 
production and pollen shed. 
• The probable reasons were the inhibition of swelling of pollen grains, 
indehiscence of anthers and poor release of pollen grains (Matsui et al. 
2000, 2005), and thus fewer numbers of pollen grains were available to be 
intercepted by the stigma. 
• This swelling of pollen grains in the locules is the driving force for anther 
dehiscence (Matsui et al. 1999) 
• Exposure of pollen grains to high temperature resulted in a loss of pollen 
viability within 10 min (Song et al. 2001) 
• The stigma is less sensitive to heat than the anther and pollination of the 
• Stigma with unstressed pollen generally restores the spikelet fertility 
(Yoshida et al.1981).
• Albinism is the absence of chlorphyll producing a white spikelet or panicle under 
heat stress 
• Significant genotypic variations in high temperature induced floret sterility exist. 
• The decrease in spikelet fertility can be termed a phenotypic character of rice plant 
under high temperature, while the decrease in pollen germination and activity can be 
considered as the physiological factors responsible for this decrease (Tang et al. 
2008). 
• Exogenous application of growth regulators has been shown recently to have some 
positive effects on the spikelet fertility and pollination (Mohammed & Tarpley 2009). 
• In fact, their exogenous application increased the level of endogenous antioxidants 
and thus prevented the oxidative damage to the membranes in rice (Mohammed & 
Tarpley 2009).
Role of humidity in spikelet sterility at high temperature 
• Higher relative humidity (RH) at the flowering stage under 
increased temperature affects spikelet fertility negatively (Yan et al. 
2010). 
• Relative humidity of 85–90 % at the heading stage induced almost 
complete grain sterility in rice at a day / night temperature of 35/30 
°C (Abeysiriwardena et al.2002). 
• The temperature inside the spikelet decreases with a reduction in 
RH, possibly due to the enhancement of transpiration at low RH 
(Weerakoon et al.2008).
Table: Symptoms of heat stress in rice plants 
Growth 
Threshold 
stage 
temperature 
(OC) 
Symptoms References 
Emergence 40 Delay and decrease in 
emergence 
Yashida (1978), 
Akman (2009) 
Seedling 35 Poor growth of the seedling Yashida (1981) 
Tillering 32 Reduced tillering and 
height 
Yashida (1978) 
Booting - Decresed no of pollen 
grains 
Shimazaki et al (1964) 
Anthesis 33.7 Poor anther dehiscence and 
sterility 
Jagadish et al 2007 
Flowering 35 Floret sterility Satake & Yashida 
(1978) 
Grain 34 Yield Morita et al 2004 
Ripening 29 Reduced grain filling Yashida (1981)
PHYSIOLOGICAL AND BIOCHEMICAL MECHANISMS OF 
HEAT TOLERANCE 
 Heat tolerance is generally defined as the ability of the plant to grow and 
produce economic yield under high temperature (Wahid et al. 2007). 
 True heat tolerance at sensitive stages might be conferred by protecting 
structural proteins, enzymes and membranes from heat damage. 
 High temperatures generally induce the expression of HSPs and suppress, at 
least in part, the synthesis of normal cellular proteins. 
 These HSPs can help in coping with heat stress by improving photosynthesis, 
partitioning of assimilate, nutrient and water use efficiency and membrane 
thermal stability (Wahid et al. 2007). 
 Disruption of some plant growth hormones such as ethylene, salicylic acid, 
abscisic acid, calcium and hydrogen peroxide through mutation affected the 
thermo-tolerance capability of the plants, although the levels of accumulated 
HSPs did not vary from their wild types in these mutated plants (Larkindale et 
al.2005). 
 Another prominent alteration is the modification of antioxidant enzymes, and 
alteration of membrane composition and structure (Stone 2001).
MITIGATING STRATEGIES FOR THE FORTHCOMING 
WARMER CLIMATE: 
 Replacement of the sensitive cultivars by tolerant cultivars in the fields will 
increase the global rice production. 
 From the management point of view, it is essential to adjust the duration of 
varieties such that they avoid peak stress periods. And for this purpose, the 
development of varieties 
 Site-specific adjustments in cropping systems may be needed because the effect 
of these changes in climatic factors varies with the region. 
 Management practices such as saturated soil culture (SSC), alternate wetting and 
drying (AWD) and aerobic rice cultivation in the case of drought stress, while 
growing improved varieties containing thesub1 gene in flooded soils, offer some 
adaptive options for the indirect stresses related to temperature increase. 
 The use of some growth regulators like MeJA (for advancing theflowering time 
to early morning), salicylic acid and glycine betaine (for increasing the percent 
pollen germination and spikelet fertility) will be also useful in mitigating the 
yield reduction threats.

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Effect of high temperature on rice growth, yield & grain quality

  • 1. Effect of High Temperature on Rice Growth, Yield & Grain Quality By MEDIDA SUNIL KUMAR
  • 2. Climate Change & Rice • Rice is a globally important cereal crop and as a primary source of food accounts for 35-75% of calories intake of more than 3 billion humans. • Climate change will cause tremendous damage to rice production sector if not addressed properly. Low rice supply along with increasing demand not only affects food security but also the economy of the country. • Reduce rice production in a sizable portion • Drought affects all stages of rice growth and development. The strong effects of drought on grain yield are largely due to the reduction of spikelet fertility and panicle exertion. • Climate change may also affect weed ecology, the evolution of weed species over time, and the competitiveness of C3 vs C4 weed species.
  • 3. Cardinal Temperatures of rice • Critical low temperature -15oC • Optimum Temperature -20-30oC • Critical high temperature - 45oC
  • 4. Role of Temperature on Growth & Development
  • 5. Table: Effect of temperature on germination percentage Temperature Period Germination percent 0-5o C >30 days 90 25o C 6 days 90 31-36 o C 2 days 90
  • 6. Seedling growth • Growth rate linearly increases between 22 & 31OC • Temperatures of of 22oC or below are considered subnormal for seedling growth. • Seedling growth may be reasonably good up to 35oC, above which declines sharply. • Seedlings will die above 40oC. • Optimum temperature for cell division of the radicle is 25oC and cell enlargement is 30oC. • Elongation of radicle stops below 15oC and above 40oC
  • 7. Leaf emergence • Temperature is a principle environmental determinant of leaf appearance in rice. • As per the temperature summation index the development of one leaf requires about 100 degree days before initiation of panicle primordia.
  • 8. Tillering • High temperature increases tillers • At 3-5 weeks after sowing temperature only slightly affected the tillering rate and RGR except lowest temperatures (Below 22oC). • Higher temperatures may effect the synchronism and in the mobilization of assimilates and nutrients among he tillers
  • 9.
  • 10.
  • 11. • The optimum temperature for the normal development of rice ranges from 27 to 32 °C. • A temperature increase of 1 °C shortened the number of days from sowing to heading by 4–5 days for some genotypes (Nakagawa et al 2001).  Flowering and to a lesser extent the preceding stage booting are considered to be the stages of development most susceptible to temperature in rice (Satake & Yoshida 1978; Farrell et al. 2006)
  • 12. HIGH TEMPERATURE AND SPIKELET STERILITY • Temperatures higher than the optimum induced floret sterility and thus decreased rice yield (Nakagawa et al. 2003). Spikelet sterility was greatly increased at temperatures higher than 35 °C (Matsui et al 1997). • In greenhouse experiments with both indica and japonica genotypes, Jagadish et al (2007) found that less than 1 h of exposure to temperatures above 33·7 °C was sufficient to induce sterility. • Enhanced O2 levels may further aggravate this problem, possibly because of reduced transpirational cooling (Matsui et al 1997a). • Exposure to 41 °C for 4 h at flowering caused irreversible damage and plants became completely sterile (IRRI 1976) whereas this high temperature (41 °C) had no effect on spikelet fertility at 1 day before or after flowering (Yoshida et al 1981). • There is genotypic variation in spikelet sterility at high temperature in both the sub-species of O. sativa, indica and japonica (Matsui et al. 2001; Prasad et al. 2006), which can be defined by different temperature thresholds (Nakagawa et al 2003). • However, in general, indica is more tolerant to higher temperatures than japonica (Satake & Yoshida 1978).
  • 13. Mechanism of heat-induced floret sterility • Male reproductive system in rice is known to be more sensitive to heat stress (Wassmann et al. 2009a). Prasad et al. (2006) reported that high temperature stress during rice flowering led to decreased pollen production and pollen shed. • The probable reasons were the inhibition of swelling of pollen grains, indehiscence of anthers and poor release of pollen grains (Matsui et al. 2000, 2005), and thus fewer numbers of pollen grains were available to be intercepted by the stigma. • This swelling of pollen grains in the locules is the driving force for anther dehiscence (Matsui et al. 1999) • Exposure of pollen grains to high temperature resulted in a loss of pollen viability within 10 min (Song et al. 2001) • The stigma is less sensitive to heat than the anther and pollination of the • Stigma with unstressed pollen generally restores the spikelet fertility (Yoshida et al.1981).
  • 14. • Albinism is the absence of chlorphyll producing a white spikelet or panicle under heat stress • Significant genotypic variations in high temperature induced floret sterility exist. • The decrease in spikelet fertility can be termed a phenotypic character of rice plant under high temperature, while the decrease in pollen germination and activity can be considered as the physiological factors responsible for this decrease (Tang et al. 2008). • Exogenous application of growth regulators has been shown recently to have some positive effects on the spikelet fertility and pollination (Mohammed & Tarpley 2009). • In fact, their exogenous application increased the level of endogenous antioxidants and thus prevented the oxidative damage to the membranes in rice (Mohammed & Tarpley 2009).
  • 15. Role of humidity in spikelet sterility at high temperature • Higher relative humidity (RH) at the flowering stage under increased temperature affects spikelet fertility negatively (Yan et al. 2010). • Relative humidity of 85–90 % at the heading stage induced almost complete grain sterility in rice at a day / night temperature of 35/30 °C (Abeysiriwardena et al.2002). • The temperature inside the spikelet decreases with a reduction in RH, possibly due to the enhancement of transpiration at low RH (Weerakoon et al.2008).
  • 16.
  • 17. Table: Symptoms of heat stress in rice plants Growth Threshold stage temperature (OC) Symptoms References Emergence 40 Delay and decrease in emergence Yashida (1978), Akman (2009) Seedling 35 Poor growth of the seedling Yashida (1981) Tillering 32 Reduced tillering and height Yashida (1978) Booting - Decresed no of pollen grains Shimazaki et al (1964) Anthesis 33.7 Poor anther dehiscence and sterility Jagadish et al 2007 Flowering 35 Floret sterility Satake & Yashida (1978) Grain 34 Yield Morita et al 2004 Ripening 29 Reduced grain filling Yashida (1981)
  • 18. PHYSIOLOGICAL AND BIOCHEMICAL MECHANISMS OF HEAT TOLERANCE  Heat tolerance is generally defined as the ability of the plant to grow and produce economic yield under high temperature (Wahid et al. 2007).  True heat tolerance at sensitive stages might be conferred by protecting structural proteins, enzymes and membranes from heat damage.  High temperatures generally induce the expression of HSPs and suppress, at least in part, the synthesis of normal cellular proteins.  These HSPs can help in coping with heat stress by improving photosynthesis, partitioning of assimilate, nutrient and water use efficiency and membrane thermal stability (Wahid et al. 2007).  Disruption of some plant growth hormones such as ethylene, salicylic acid, abscisic acid, calcium and hydrogen peroxide through mutation affected the thermo-tolerance capability of the plants, although the levels of accumulated HSPs did not vary from their wild types in these mutated plants (Larkindale et al.2005).  Another prominent alteration is the modification of antioxidant enzymes, and alteration of membrane composition and structure (Stone 2001).
  • 19. MITIGATING STRATEGIES FOR THE FORTHCOMING WARMER CLIMATE:  Replacement of the sensitive cultivars by tolerant cultivars in the fields will increase the global rice production.  From the management point of view, it is essential to adjust the duration of varieties such that they avoid peak stress periods. And for this purpose, the development of varieties  Site-specific adjustments in cropping systems may be needed because the effect of these changes in climatic factors varies with the region.  Management practices such as saturated soil culture (SSC), alternate wetting and drying (AWD) and aerobic rice cultivation in the case of drought stress, while growing improved varieties containing thesub1 gene in flooded soils, offer some adaptive options for the indirect stresses related to temperature increase.  The use of some growth regulators like MeJA (for advancing theflowering time to early morning), salicylic acid and glycine betaine (for increasing the percent pollen germination and spikelet fertility) will be also useful in mitigating the yield reduction threats.