Contents

1 Introduction

Various environmental stresses affecting plant growth and development have attained a serious concern in the context of possible climate change. Contemporary agriculture faces a tremendous environmental pressure across the globe. Foley et al. (2011) suggested several management options including conservation tillage, adopting yield gap strategies, increasing cropping efficiencies that could be greatly effective to minimize environmental impacts and for sustainable crop production. However, the most remarkable environmental concern in agriculture is the increase of global temperature. With regard to global climate models, the mean ambient temperature is predicted to increase by 1–6°C by the end of twenty-first century (De Costa 2011). Such increase of global temperature may have a significant influence on agricultural productivity in accordance with the severity of the high temperature, drought, salinity, waterlogging, and mineral toxicity stresses. High temperature-induced heat stress is expressed as the rise in air temperature beyond a threshold level for a period sufficient to cause injury or irremediable damage of crop plants in general (Teixeira et al. 2013). The heat stress situation is aggravated when soil temperature increases as a result of increase in air temperature associated with decline in soil moisture. Thus, heat stress has appeared as a great menace to successful crop production in the world (Kumar et al. 2012; Lobell and Gourdji 2012; Gourdji et al. 2013).

Wheat (Triticum aestivum L.), the most widely cultivated cereal crop belonging to Poaceae family, is the largest contributor with nearly 30% of the world grain production and 50% of the world grain trade. FAO estimated that the world would require additional 198 million tonnes of wheat by 2050 to accomplish the future demands, for which wheat production need to be increased by 77% in the developing countries (Sharma et al. 2015). However, the temperature anomaly distribution is changing toward higher temperatures and the anomalies are increased (Hansen et al. 2012). Such a situation over the crop growing season has already been reported to reduce wheat productivity in the many regions of the world (Fontana et al. 2015; Mueller et al. 2015). Some indicators of heat stress effects in wheat are illustrated in Fig. 1.

Fig. 1
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Indicators of heat stress are stay green characteristics, rapid ground coverage and early heading and phenology (photo from a USDA research project)

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Wheat is very receptive to heat stress (Gupta et al. 2013a). Low latitude zones, where around 100 million hectares of wheat are cultivated, are predominantly heat prone areas worldwide (Braun et al. 2010). Asseng et al. (2014) tested 30 wheat crop models where mean temperatures in the growing season ranged from 15 to 32°C with artificial heating. The results obtained indicate that warming already decreased grain yield at a majority of the wheat-growing locations. The simulated median temperature impact on declining wheat yield varied widely, and the average yields for the periods between 1981 and 2010 decreased; ranging between 1 and 28% across 30 sites of the world; for an increase in temperature of 2°C; and this value rose to between 6 and 55% for a temperature of 4°C. Also they estimated that global wheat production falls by 6% for each 1°C of further temperature increase. The low latitudes showed a marked increase in simulated yield variability with higher temperature than that observed at high latitudes. This greater relative yield decline was due to the higher reference temperature (Challinor et al. 2014). Mondal et al. (2013) stated that the effects of heat stress on plants are very complex resulting in alteration of growth and development, changes in physiological functions, and reduced grain formation and yield (Fig. 2). Heat stress causes alteration of plant water relations (Hasanuzzaman et al. 2012, 2013), reduction of photosynthetic capacity (Almeselmani et al. 2012; Ashraf and Harris 2013), decreases of metabolic activities (Farooq et al. 2011) and changes of hormones (Krasensky and Jonak 2012), production of oxidative reactive species (Wang et al. 2011), promotion of ethylene production (Hays et al. 2007), reduction of pollen tube development, and increases of pollen mortality (Oshino et al. 2011) in wheat. During the period from 1880 to 2012, the Earth’s system warmed by 0.85°C (IPCC 2014). This warming period will continue and is predicted to rise between the range of 1.5–4.0°C in the future (Wheeler and Von Braun 2013). The climatic factors like changes in temperature, precipitation, CO2, weather variability, and soil moisture deficit would have positive or negative effects on crop production (Joshi and Kar 2009). The deleterious impacts of climate change on crop production are challenging the food security of the world, and it is predicted that sustaining wheat production will be impacted more by increasing temperature (Tripathi et al. 2016). Climate change could strongly affect wheat production, accounting for 21% of food and 200 million hectares of farmland worldwide (Ortiz et al. 2008).

Fig. 2
figure 2

Major effects of heat stress on plants growth and development. Pn, Rs, and Ci indicate photosynthesis, stomatal conductance, and intercellular CO2 concentration, respectively

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Climate change impacts on crop production are highly diverse. Deryng et al. (2014) contributed greatly to current understanding of climate change impacts on crops under heat stress and elevated CO2 environment. The heat stress occurs usually for rising of canopy temperature that depends on air and soil temperature, soil and canopy properties, and loss of soil moisture (Fig. 3). High temperature affects crops in different ways including poor germination and plant establishment, reduced photosynthesis, leaf senescence, decreased pollen viability, and consequently production of less grains with smaller grain size (Ugarte et al. 2007; Asseng et al. 2011). Such effect varies depending on the crops, cultivars, and phenological stages. Due to global warming and changes in the climate pattern, it is imperative to determine the effects of heat stress and possible ways of improving heat tolerance for the success of wheat production under heat stress environment. Reidsma et al. (2010) approached various models of adaptation measures based on climate impact assessment. Deryng et al. (2014) considered choice of cultivars and changing sowing dates as adaptive measures under extreme heat stress conditions. Some other adaptation measures are surface cooling by irrigation (Lobell et al. 2008), antioxidants defense (Suzuki et al. 2011; Caverzan et al. 2016), and osmoprotectants (Farooq et al. 2011; Kaushal et al. 2016).

Fig. 3
figure 3

Schematic illustration of linking between climate-induced heat stress occurrence, plant responses to heat stress, and adaptation measures in the farmers’ field

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Fig. 4
figure 4

Schematic diagram showing the exploration of wheat genetic resources and identifying wheat genotypes tolerant to heat stress, breeding strategies followed for genetic enhancement of diverse wheat genetic resource and adaptation strategies needed for managing genotypes considering phenology under heat stress environment for high yield potentials

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However, development of heat-tolerant wheat varieties and generation of improved pre-breeding materials for any breeding program in future is crucial in meeting the food security (Ortiz et al. 2008). Proteomic and transcriptomic data are important to identifying genes and proteins that respond to environment, and affects yield and quality of wheat. However, more information regarding this is required to develop wheat variety that can adapt to climate change-induced high temperature (Altenbach 2012). In this context, this review covers an overview of the current work reported on heat-induced adverse effects and various crucial management strategies to address the heat stress situation in wheat.

2 Plant responses to heat stress

Heat stress affects various plant processes leading to morpho-physiological alterations in wheat plants, hindering the development processes and eventually resulting into great yield loss (McClung and Davis 2010; Grant et al. 2011). Plant responses to heat stress differ significantly with the extent and duration of temperature, and the growth stages encountering the stress (Ruelland and Zachowski 2010). Some common effects of heat stress on growth and productivity, grain development, and yield of wheat are presented in Table 1.

Table 1 Effects of heat stress at different stages of growth and development of wheat
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2.1 Morphological and growth responses

The primary effect of heat stress is the impediment of seed germination and poor stand establishment in many crops including wheat (Johkan et al. 2011; Hossain et al. 2013). Ambient temperature around 45°C severely affects embryonic cell in wheat which reduces crop stands through impairing seed germination and emergence (Essemine et al. 2010). Heat stress mostly affects the plant meristems and reduces plant growth by promoting leaf senescence and abscission, and by reducing photosynthesis (Kosova et al. 2011). Heat stress ranging from 28 to 30°C may alter the plant growth duration by reducing seed germination and maturity periods (Yamamoto et al. 2008). Warm environment produces lower biomass compared to plants grown under optimum or low temperature. Day and night temperature around 30 and 25°C, respectively, may have severe effects on leaf development and productive tiller formation in wheat (Rahman et al. 2009). However, the prevalence of reproductive stage heat stress has been found to be more detrimental in wheat production (Nawaz et al. 2013). One degree rise in average temperature during reproductive phase can cause severe yield loss in wheat (Bennett et al. 2012; Yu et al. 2014). High temperature stress degenerates mitochondria, changes the protein expression profiles, reduces ATP accumulation, and oxygen uptake in imbibing wheat embryos, resulting in increased occurrence of loss of seed quality relating to seed mass, vigor, and germination (Balla et al. 2012; Hampton et al. 2013). Increase in temperature of 1–2°C reduces seed mass by accelerating seed growth rate and by shortening the grain-filling periods in wheat (Nahar et al. 2010).

2.2 Physiological responses

2.2.1 Water relations

Plant water status is generally found to be most erratic under changing ambient temperature. High temperature seems to cause dehydration in plant tissue and subsequently restricts growth and development of plants. During flowering, a temperature of 31°C is generally considered as an upper limit of maintaining water status of a crop (Atkinson and Urwin, 2012). With a concomitant increase in leaf temperature, wheat plants exposed to heat stress substantially decrease the water potential and the relative water content in leaves, and eventually reduce photosynthetic productivity (Farooq et al. 2009). Simultaneously, the rate of transpiration and plant growth are severely affected. Almeselmani et al. (2009) observed that high temperature (35/25°C) imposed after tillering showed a significantly reduction of water potential in wheat, and the reduction was higher in genotypes susceptible to heat stress. In general, different antioxidants are associated with dehydration tolerance and are stimulated under heat stress. This is because of increased transpiration in stressed leaf and dropping of osmotic potential (Ahmad et al. 2010). Heat stress also increases hydraulic conductivity of cell membrane as well as plant tissues primarily for increased aquaporin activity (Martinez-Ballesta et al. 2009) and to a greater extent for reduced water viscosity (Cochard et al. 2007).

2.2.2 Photosynthesis, photosystems, and leaf senescence

Photosynthesis is the most sensitive physiological event leading to poor growth performance in wheat (Feng et al. 2014). A major effect of heat stress is the reduction in photosynthesis resulting from decreased leaf area expansion, impaired photosynthetic machinery, premature leaf senescence, and associated reduction in wheat production (Ashraf and Harris 2013; Mathur et al. 2014). The reaction sites of heat-induced injury are stroma and thylakoid lamellae of chloroplast where carbon metabolism and photochemical reactions occur, respectively. In wheat, heat stress causes disruption of thylakoid membranes, thereby inhibiting the activities of membrane-associated electron carriers and enzymes, which ultimately results in a reduced rate of photosynthesis (Ristic et al. 2008). The inactivation of chloroplast enzymes, mainly induced by oxidative stress, may also reduce the rate of leaf photosynthesis. Reduction of net photosynthetic rate due to heat stress is often attributed to increased non-photorespiratory processes (Ainsworth and Ort 2010). The researchers opined that impediment of photosynthetic activities is the result of reduced soluble protein, Rubisco and Rubisco binding proteins (Parry et al. 2011; Hasanuzzaman et al. 2013). Wheat leaf exposed to a high temperature around 40°C either in dark or light causes a great change in Rubisco and Rubisco activase and such changes are irreversible under dark conditions (Mathur et al. 2011).

In photosynthesizing tissues, photosystem-II is much responsive to heat stress (Marutani et al. 2012) but photosystem-I is relatively stable (Mathur et al. 2014). Heat stress firstly, damages the complex phenomena of photosystem-II and secondly, changes the photosynthetic behavior. The stress causes suppression of carbon assimilation due to inactivation of Rubisco activase in wheat. The reduction of carbon assimilation reduces ROS generation which, in turn, reduces protein synthesis and inhibits repairing of damaged photosystem-II (Murata et al. 2007; Allakhverdiev et al. 2008). Prasad et al. (2008a) also explained the sensitivity of photosystem-II where increasing fluidity of thylakoid membrane and transport of electron to heat stress are commonly observed. It is manifested that temperature >40°C dissociates the light harvesting complex-II Chl a/b-proteins from the photosystem-II (Iwaia et al. 2010). Heat stress damaging and disordering of thylakoid membranes is also responsible for the cessation of photophosphorylation (Dias et al. 2009a). At high temperature, the key regulatory enzyme of Rubisco, i.e., Rubisco activase is reported to be dissociated causing a reduction in the photosynthetic capacity of leaf in wheat (Raines 2011).

Leaf senescence is one of the inimitable symptoms of heat injury characterized by structural changes in the chloroplast followed by a vacuolar collapse, and thereafter a loss of plasma membrane integrity and interference of cellular homeostasis (Khanna-Chopra 2012). Thus, heat stressed wheat plants have been found to be experienced senescence-related metabolic changes (Ciuca and Petcu 2009). Inhibition of chlorophyll biosynthesis under heat stress (>34°C) may hasten leaf senescence in wheat (Asseng et al. 2013). Wheat plant exposed to heat stress during maturity enhanced leaf senescence, accentuated the loss of chloroplast integrity, and accelerated the turn-down of photosystem-II-mediated electron transport (Haque et al. 2014). However, a large diurnal variation in temperature is also responsible for the promotion of flag leaf senescence in wheat (Zhao et al. 2007).

2.2.3 Oxidative damage

Plants exposed to heat stress often leads to the generation of destructive ROS, including singlet oxygen (1O2), superoxide radical (O2−), hydrogen peroxide (H2O2), and hydroxyl radical (OH−) responsible for generating oxidative stress (Marutani et al. 2012; Suzuki et al. 2012). Oxidative stress notably increased membrane peroxidation and decreased membrane thermo-stability in many plants including wheat (Savicka and Skute 2010). Hydroxyl radicals react with almost all constituents of cells. Continual heat stress in plants may cause accumulation of ROS in cell plasma membrane with depolarization of cell membrane, activation of ROS-producing enzyme RBOHD and trigger of programmed cell death (Mittler et al. 2011). Miller et al. (2009) found that heat stress increased O2—production in root by 68% and malondialdehyde (MDA) content in leaf by 27% at the early stages, and 58% at the later stage of seedling development. However, plants have antioxidant mechanisms for escaping the excess ROS. Several studies have shown that antioxidants superoxide dismutase (SOD), ascorbate peroxidase (APX) and catalase (CAT) glutathione reductase (GR), and peroxidase (POX) have ameliorating effects of heat stress in wheat (Suzuki et al. 2011; Caverzan et al. 2016).

2.2.4 Respiration

Heat stress changes mitochondrial activities by affecting respiration. The rate of respiration increases with increasing temperature, but at a certain level of temperature, it diminishes due to damage of respiratory apparatus (Prasad et al. 2008b). The increased rate of respiratory carbon loss due to heat stress in the rhizosphere reduced production of ATP and enhanced the generation of ROS (Huang et al. 2012). This is because heat stress affects the solubility of CO2 and O2, and the kinetics of Rubisco (Cossani and Reynolds 2012). Almeselmani et al. (2012) observed that the rate of respiration in flag leaf of wheat was significantly higher in heat susceptible varieties under heat stress (35/25°C day/night) when compared with that of control (23/18°C day/night).

2.3 Grain growth and development

The optimum temperature for wheat anthesis and grain filling ranges from 12 to 22°C (Shewry 2009). Plants exposed to temperatures above >24°C during reproductive stage significantly reduced grain yield and yield reduction continued with increasing duration of exposure to high temperature (Prasad and Djanaguiraman 2014).

2.3.1 Grain number, grain filling, and grain quality

Heat stress reduces the number of grains leading to lower harvest index in wheat (Lukac et al. 2011). However, the influence of heat stress on both the number and size of grains varies with the growth stages encountering heat stress. For instance, temperatures above 20°C between spike initiation and anthesis speed up the development of the spike but reduce the number of spikelets and grains per spike (Semenov 2009). Heat stress adversely affects pollen cell and microspore resulting into male sterility (Anjum et al. 2008). Even high temperature of above 30°C during floret development may cause complete sterility in wheat depending on genotypes (Kaur and Behl 2010). In wheat, the anther produced under 3 days heat stress during anthesis was found to be structurally abnormal and nonfunctional florets (Hedhly et al. 2009). Day/night high temperature of 31/20°C may also cause shrinking of grains resulting from changing structures of the aleurone layer and cell endosperm (Dias et al. 2008).

Grain-filling stage in wheat is very sensitive to high temperature (Farooq et al. 2011). Heat stress generally accelerates the rate of grain-filling and shortens the grain-filling duration (Dias and Lidon 2009a). However, the grain growth rate and duration decreased in plants having different grain weight stability (Vijayalakshmi et al. 2010). In wheat, grain-filling duration may be decreased by 12 days with the increase of 5°C temperature above 20°C (Yin et al. 2009). The increase in night temperature is more responsive, shortens the grain-filling period, and reduces the grain yield than that of day temperature. Night temperatures of 20 and 23°C reduced the grain-filling period by 3 to 7 days (Prasad et al. 2008a). Recently, Song et al. (2015) observed a significant reduction in the rate of grain filling in wheat cultivars at day/night temperature of 32/22°C when compared with that of 25/15°C.

Heat stress affects grain quality of many cereals and legumes, essentially because of limitation of assimilates and less remobilization of nutrients. Heat stress hardly affects the protein concentration of grain in wheat (Lizana and Calderini 2013), but a strong correlation was observed between leaf nitrogen content and grain protein (Iqbal et al. 2017). However, wheat plants are capable of adopting a heat shock by developing thermo-tolerance for the improvement of the grain quality and yield (Sharma-Natu et al. 2010). Although build-up of protein in wheat grain is not significant under heat stress, the processing quality traits are reported important. Li et al. (2013) found that heat tends to diminish flour quality by reducing gluten strength-related parameters lactic acid retention capacity and mixograph peak time. However, wheat plants experiencing heat stress early in grain filling were found to have high content of grain protein (Castro et al. 2007). Increased grain protein content is associated with sedimentation index and intensity of essential amino acids. With decreased levels of amino acids, heat stress decreases the sedimentation index (Dias et al. 2008).

2.3.2 Starch synthesis

Wheat grain contains 60–75% starch of its total dry weight (Sramkova et al. 2009). Heat stress significantly limits starch biosynthesis in grains of wheat but caused a remarkable increase in total soluble sugar and protein (Sumesh et al. 2008; Asthir and Bhatia 2014). Liu et al. (2011) observed that heat-shock treatment above 30°C resulted in a significant increase of grain starch and limited the dry matter accumulation in grain of wheat. Around 97% of activity was lost due to the decrease in soluble starch synthase at 40°C, resulting in reducing grain growth and starch accumulation in wheat (Chauhan et al. 2011). High temperature stress (35/27°C) imposed at seedling stage significantly reduce soluble sugar accumulation and biomass yield in wheat (Wang et al. 2014).

2.3.3 Translocation of photosynthetic products

Photosynthetic products in the form of sucrose and glutamine are essentially translocated to the reproductive sinks for seed development. Under heat stress conditions, the source and sink limitations may reduce the growth and development of crop plants. Seed-set and -filling can also be restricted by source and/or sink limitations (Lipiec et al. 2013). When photosynthesis is inhibited by heat stress, stem reserves during pre-anthesis period are recognized as source of carbon for supporting grain filling (Mohammadi et al. 2009). In wheat, heat stress reduced N remobilization. The grain filling of wheat is seriously impaired by heat stress due to reduction in current leaf and ear photosynthesis. In case of heat-induced source limitation, plants seek to explore alternative source of assimilates to remobilize into the grains. At this time, stem reserves of water soluble carbohydrate and its greater translocation to reproductive organs are vitally important for supporting grain growth and development (Talukder et al. 2013). However, assimilate translocation occurring through both symplastic and apoplastic pathway is substantially reduced at high temperature. High temperature at the pre-anthesis period increased carbohydrate translocation from stem to grain resulting to less reduction of starch content in grains of wheat at the post-anthesis heat stress (Wang et al. 2012). In future, research directing to assimilate partitioning and phenotypic flexibility is suggested by Iqbal et al. (2017).

3 Managing heat stress

It is evident that heat stress adversely affects the growth and development of wheat plants. Such effects can be managed principally through producing appropriate plant genotypes together with adjustment of relevant agronomic practices (Asseng et al. 2011; Chapman et al. 2012). Various efforts have been made to produce heat-tolerant genotypes using the knowledge gained until now on the responses of wheat plant to heat stress. For sustainable wheat production in heat-stressed areas, the two most imperative strategies can be followed: (a) introduction of genetically modified or transgenic wheat cultivars by selecting molecular and biotechnological means coupled with conventional breeding approaches and (b) inducing several agronomic management strategies so far experiencing heat stress management under field conditions. A schematic diagram showed identification of wheat genotypes tolerant to heat stress, and breeding and adaptation strategies for managing wheat genotypes under heat stress environment (Fig. 4).

3.1 Genetic management

Breeding is an adaptation response of crops under changing environment. Therefore, it requires the evaluation of genetic diversity for adaptation to future climate change conditions, and thereby the selection and induction of stress inducible genes of genetic resources for developing new varieties in the production systems (Chapman et al. 2012). Breeding for heat tolerance is still in the preliminary stage and therefore, much attention is given to the genetic improvement of wheat to heat stress. In recent years, several studies have been done to find out wheat genotypes tolerant to heat stress (Kumar et al. 2010; Sareen et al. 2012; Kumari et al. 2013; Nagar et al. 2015).

3.1.1 Screening and breeding for heat tolerance

In breeding program, various physiological approaches have been found to be effective in Australia and several developing countries. The methodology includes screening genetic resources for identification of genetic bases for heat tolerance in crops. From this, a desired new plant types can be developed following physiological crossing of novel trait combinations, to combat future climate that comprises high temperature events (Reynolds and Langridge 2016). Screening wheat genotypes under natural heat stress condition in various spatial environments is difficult. Therefore, no consistent selection criterion has been established to evaluate diverse genetic materials for tolerance to heat stress. Selection criteria and screening methods for identifying better wheat genetic materials tolerant to heat stress are generally approached based on characteristics associated with higher grain yield under the adverse heat stress situation. In this regards, researchers suggested some indirect selection criteria for developing heat tolerance in wheat (Table 2).

Table 2 Selection criteria of wheat genetic resources for tolerance to heat stress
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Table 3 Plant responses to exogenous protectants under heat-stressed conditions
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Sharma et al. (2013) found susceptibility index as a consistent parameter while selecting wheat genotypes tolerant to heat stress. Mason et al. (2010) have given emphasis on quantitative trait loci (QTL) mapping of each yield attributes as susceptibility index and its collective contribution to heat tolerance and grain yield stability. Recent data shows that thylakoid membrane stability is highly associated with the heat tolerance capacity of wheat. Mass screening using stay-green character may be done for heat tolerance of wheat genotypes. Kumar et al. (2010) followed this method in evaluating stay-green trait of wheat and found a correlation with terminal heat tolerance in wheat. In general, morphological traits like early ground cover, leaf rolling, biomass, and also several physiological traits, such as leaf chlorophyll content, photosynthetic rate, flag leaf stomatal conductance, membrane thermostability, and stem reserves have been found to be associated with cellular thermotolerance in wheat plants. Recent advances in molecular science contributed greatly to understand the complexity of stress response mechanisms under heat stress conditions. Asthir (2015a, b) emphasized on the knowledge of molecular pathways and protective mechanisms to breed heat stress-tolerant plants. Heat tolerance is obviously a polygenic trait, and the above tools also aid in analyzing the genetic basis of plant thermotolerance. Wang et al. (2016) proposed a useful utilization of some transcription factors to improve multiple stress tolerance of crops. QTL mapping and subsequent marker-assisted selection made it possible to better understanding the heat tolerance in plants (Heffner et al. 2009). Recent studies reveal that several QTLs are available and can be used for developing heat tolerance in wheat. For example, QTLs for heat tolerance has been identified for grain weight and grain-filling duration (Mason et al. 2010; Paliwal et al. 2012), senescence-related traits (Vijayalakshmi et al. 2010), and canopy temperature (Paliwal et al. 2012). Mason et al. (2010) also identified QTLs related to yield and yield attribute traits and suggested that the spike of wheat could be used for locating QTL’s genomic zone for heat tolerance. Besides, others recognized QTLs on chromosomes 2B and 5B and 4A in wheat under heat stress conditions (Pinto et al. 2010). The electrolyte leakage is an indication of reduced cell membrane thermo-stability (CMT) and reflects the performance of wheat genotypes subjected to in vitro heat shock. Genotypes generating heat shock proteins (HSPs) can withstand heat stress as they protect proteins from heat-induced damage (Farooq et al. 2011). The genotypic differences in CMT tolerance in wheat at different growth stages were also reported (Kumar et al. 2013b; Asthir et al. 2013). The findings also suggested that the abundance of small heat shock protein and superoxide dismutase during milky-dough stage plays a vital role in the biosynthesis of starch granule, and this will help to develop heat-tolerant wheat cultivars containing high quality grains. For this, a simple, quick, and less costly screening method is required for a large number of germplasm to develop heat-tolerant wheat cultivars. As such, SPAD chlorophyll meter could be used for high throughput screening of wheat germplasm for heat tolerance (Ristic et al. 2007).

3.1.2 Biotechnological approach for improving heat tolerance

Genetic engineering and transgenic approaches can alleviate the adverse effects of heat stress by improving heat tolerance (Chapman et al. 2012). It involves the incorporation of genes of interest into the desired plants to improve plant tolerance to heat stress (Zheng et al. 2012). However, the complexity of the genomic pattern makes it difficult to research for genetic modification in wheat. Heat stress for a longer period increases protein synthesis elongation factor (EF-Tu) in chloroplast which is associated with heat tolerance in wheat. The constitutive expression of EF-Tu in transgenic wheat protected leaf proteins against thermal aggregation, reduced thylakoid membranes disruption, enhanced photosynthetic capability, and resisted pathogenic microbes infection (Fu et al. 2012). The wheat genotypes accruing more EF-Tu showed better tolerance to heat stress than those exposed to less EF-Tu (Ristic et al. 2008). Recently, many transcription factors (TFs) involved in various abiotic stresses have been found and engineered to improve stress tolerance in crops (Wang et al. 2016). Genome sequences of many plants are recently generated for improvement of stress tolerance. Clavijo et al. (2016) confirmed three known and identified one novel genome rearrangement of wheat. They used relatively inexpensive sequencing technologies and anticipated that researchers will use the approaches illustrated to sequence multiple wheat varieties. This will bring a large scale structural changes that are known to play a major role in the adaptation of the wheat crop to different stressful environments.

3.2 Agronomic management

Wheat can be grown successfully in a warmer environment through manipulating some agronomic management practices (Ortiz et al. 2008). Adoption of various agronomic practices like (i) water conserve techniques (ii) the appropriate amount and methods of fertilization (iii) maintaining proper time and methods of sowing, and (iv) the application of exogenous protectants can effectively alleviate the adverse impact of heat stress in wheat (Singh et al. 2011b).

3.2.1 Conserving soil moisture

A continuous supply of water is necessary for sustaining the grain-filling rate and duration, and grain size in wheat. This could not be possible in rain-fed wheat growing area, but here, mulching can be the best option for maintaining optimum moisture and thermal regimes in the soil system. Straw mulch conserves soil moisture by reducing soil evaporation (Chen et al. 2007). However, mulching is advocated to avoid yield reduction in wheat when reduced tillage is practiced (Glab and Kulig 2008). Increasing the productivity of wheat using mulch under heat stress and water deficit environment has been reported elsewhere (Chakraborty et al. 2008). Application of organic mulches preserves better soil moisture and improves plant growth and development, subsequently increases water and nitrogen use efficiency which may reduce (Singh et al. 2011b). This practice has been found to be very effective in wheat production under adverse heat stress conditions in temperate and tropical regions.

3.2.2 Nutrient management and planting time

Adequate and balanced supply of mineral nutrients is essential in plants exposed to temperature stress (Waraich et al. 2012). Application of nitrogen, phosphorus, and potassium at the post-anthesis period enriches grain proteins when the day and night temperatures remain 24 and 17°C, respectively, but effects are nullified for higher day and night temperature. Foliar spray of nutrients is very effective and can alleviate such adverse effect of heat stress on wheat. Application of potassium orthophosphate (KH2PO4) as a foliar spray after anthesis could be an alternative technique to increase the heat tolerance of wheat. Potassium orthophosphate causes a delay in the heat stress-induced leaf senescence and enhances grain yield (Dias and Lidon 2010). The advantages of NO3 − through delaying abscisic acid synthesis and promoting cytokinin activity, and similarly K+ induced increasing photosynthetic activities and assimilates accumulation are well recognized for increasing grain yield under heat stress environment (Singh et al. 2011a).

The exogenous application of calcium promotes heat tolerance in plants (Waraich et al. 2011). Calcium (Ca) application in the form of CaCl2 increased the malondialdehyde (MDA) content and stimulated the activities of guaiacol peroxidase, SOD, and CAT in wheat, which could be the reasons for the induction of heat tolerance. In bread wheat genotypes, Ca accumulation also seems to be linked with a higher tolerance to heat stress, possibly because this nutrient can shield chlorophylls from photo-destruction and can maintain stomata functioning, thus attenuating the heat stress effects through transpiration (Dias et al. 2009b).

Adequate supply of magnesium (Mg) was identified as an effective nutritional strategy to minimize heat stress-related losses in wheat production. Mengutay et al. (2013) found that wheat plants suffering from Mg deficiency were susceptible to heat stress, and sufficient Mg in the form of MgSO4.7H2O effectively alleviated the detrimental effect of heat stress (light/dark 35/28°C). Zinc (Zn) deficiency and heat stress also affect the wheat productivity by reducing kernel growth and chloroplast function (Peck and McDonald 2010). Heat stress generally increases Zn concentration in grain mostly due to remobilization from the shoot (Dias and Lidon 2009b). Therefore, Zn has also been proven to be effective in improving heat tolerance in wheat.

In general, late sowing wheat varieties faces severe temperature stress, shortens the heading and maturity duration, ultimately affecting final yield and grain quality (Hossain and Teixeira de Silva 2012; Hakim et al. 2012). Therefore, it is recommended for the development of high yielding wheat cultivars adapted to semiarid environments to select the genotypes with early maturity and a relatively long time to heading (Al-Karaki 2012). Hence, the early planting and the genotypes with early maturity and a relatively long time to heading are advocated to evade terminal heat stress and accelerate grain filling (Khichar and Niwas 2007; Al-Karaki 2012). Therefore, the maintaining appropriate planting time is one of the most important agronomic practices for getting optimum plant growth and yield of wheat under heat-stressed environment (Kajla et al. 2015).

Modification in planting method could alleviate the adverse impact of heat stress during the reproduction stage of wheat. Permanent bed planting under zero-tillage with crop residue retention has already been proposed as the possible means for improving heat stress tolerance in wheat plants for Northwest Mexico. Planting of wheat in conventional tillage with straw mulch increased water holding capacity, organic carbon, and total nitrogen in soil and improve tillering capacity resulting to mitigate the high temperature-induced reduction of grain weight at the late grain filling stage (Tang et al. 2013).

3.2.3 Use of exogenous protectants

In recent times, exogenously applied several growth-promoting protectants such as osmoprotectants, phytohormones, signaling molecules and trace elements have resulted in the potential to protect the plants by neutralizing the harmful and adverse effects of heat stress (Sharma et al. 2012; Upreti and Sharma 2016). Exogenously applications of these substances improve thermotolerance in wheat under heat stress by managing the ROS (Farooq et al. 2011) and upregulating the antioxidant capacity (Hemantaranjan et al. 2014). Treating thermo-sensitive wheat plants with several protectants, such as arginine, putrescine (Put), and α-tocopherol (vitamin E) have already established their roles in thermo-tolerance. External application of these molecules have ameliorating effects against oxidative stress through activation of various enzymatic viz. superoxide dismutase, catalase, ascorbate peroxidase, glutathione reductase and non-enzymatic viz. ascorbic acid, tocopherol, and glutathione antioxidants (Balla et al. 2007). The extensively used various plant bio-regulators in horticultural crops can be potentially used in field crops including wheat, and their prospects are now whipped out as in emerging stress alleviating technology in heat stress environment (Ratnakumar et al. 2016). The protective effects of exogenous application of arginine, putrescine, and tocopherol on heat-stressed wheat plants are shown in Table 3. Under abiotic stress condition, naturally occurring several intracellular polyamines (PAs), such as spermine, spermidine, and putrescine, can play vital roles for sustainable crop production. Recently, research directed towards polyamine biosynthesis, catabolism, and its role in abiotic stress tolerance is gaining priority (Gupta et al. 2013b; Rangan et al. 2014).

3.2.4 Bacterial seed treatment

Varietal improvement through the breeding program is time-consuming and costly, and gene transformation technology is not well perceived by many stakeholders. Therefore, using biological control agents like fungi and bacteria are now considered as an alternative method of improving heat tolerance (Raaijmakers et al. 2009). Plant growth-promoting rhizobacteria are found to be compatible and having a beneficial effect on the growth of wheat plants under heat stress (Nain et al. 2010). Seed treatment with rhizobacteria and foliar spray of various organic and inorganic agents enhanced heat tolerance in wheat (Yang et al. 2009). Seed inoculation with rhizobacteria also significantly improved heat tolerance in wheat (Anderson and Habiger 2012). Seed treatment with Bacillus amyloliquefaciens UCMB5113 and Azospirillum brasilense NO40 strains were also found to be effective to increase heat tolerance of wheat seedlings by reducing ROS generation (Abd El-Daim et al. 2014).

4 Conclusions and future perspective

In the recent past, heat stress was found to lead to enormous loss of wheat productivity worldwide. Despite carrying out intensive studies on the deleterious effects of heat stress in wheat, in-depth understanding of the mechanism of heat tolerance remains elusive. So, heat stress tolerance mechanism is vital for developing a notable strategy of wheat management under heat stress and forth seeing climate change settings. To generate heat-tolerant high yielding crops, metabolic and development processes associated with heat stress and energy regulation must be systematically understood. Although a considerable progress has been achieved in understanding the heat stress effects on wheat, yet there is a need for further understanding of the biochemical and molecular basis of heat tolerance for improvement of the crop yield from upcoming warmer environments. Molecular knowledge of response and tolerance mechanisms to harvest sustainable grain yields must be investigated. To recognize this, the functional genomic approach would be supportive in the response of wheat to heat stress.

It is well established that classical and modern molecular genetics tools integrated with the agronomic management practices can overcome the complexity of the heat syndrome. This is why the different biochemical and molecular approaches and agronomic options are required to explore the actual effects of heat stress on final crop yield. Moreover, the exogenous applications of protectants have revealed advantageous effects on heat tolerance improvement in wheat. Applying microorganisms seem to be a useful tool in agriculture to ameliorate the negative effects of heat stress on wheat plants, but further studies are needed to identify and optimize the parameters involved in successful microbial performance.

Thus, conventional breeding and modern biotechnological and molecular tools are an important area for future research. The actual basis of applying these methods is whether the plants contain heat tolerance or not. Wheat genotypes are found to express a substantial level of heat tolerance, although complete tolerance has not been found hitherto. Most alarming is that no selection criteria of heat tolerance have been established. Recently, heat sensitivity indexes for thousand kernel weight and grain filling duration have been developed.

Ultimately, an intimate collaboration and efforts amongst molecular biologists, plant physiologists, and breeders is required. A system-wide phenome to genome analysis is required to make possible an accurate trait mapping, introgression of superior alleles, or cloning of major QTLs for heat tolerance, and such combination will enable us to identify genes involved in heat tolerance and also the relationships between phenotypes and genotypes. For obtaining effective heat tolerance, the transgenic approach must be pooled with marker-assisted breeding programs for heat stress-related genes and QTLs.

In view of foreseen global warming, knowledge relating to molecular basis and mechanism of tolerance is considered to pave the way for engineering plants that can withstand heat stress and give satisfactory yield. Despite the fact that there is a possibility for application of EF-Tu in developing heat tolerant and disease resistant wheat varieties by modulating its expression levels, additional studies are mandatory to explore the mechanism of action of wheat EF-Tu relative to heat tolerance. It is important to note that molecular study affirms increasing economic crop yield, but full potential yield expression requires estimation of yield at crop level. So, crop modeling system studies are vital to improving heat stress tolerance and grain yield in wheat.