Hostname: page-component-76fb5796d-25wd4 Total loading time: 0 Render date: 2024-04-27T17:22:07.267Z Has data issue: false hasContentIssue false

Weather indices during reproductive phase explain wheat yield variability

Published online by Cambridge University Press:  24 November 2023

Ketema Tilahun Zeleke*
Affiliation:
School of Agricultural, Environmental and Veterinary Sciences, Charles Sturt University, Wagga Wagga, NSW 2650, Australia Gulbali Institute for Agriculture, Water and Environment, Charles Sturt University, Wagga Wagga, NSW 2650, Australia
Muhuddin Anwar
Affiliation:
Gulbali Institute for Agriculture, Water and Environment, Charles Sturt University, Wagga Wagga, NSW 2650, Australia Wagga Wagga Agricultural Institute, NSW Department of Primary Industries, Wagga Wagga, NSW 2650, Australia
Livinus Emebiri
Affiliation:
Wagga Wagga Agricultural Institute, NSW Department of Primary Industries, Wagga Wagga, NSW 2650, Australia
David Luckett
Affiliation:
Gulbali Institute for Agriculture, Water and Environment, Charles Sturt University, Wagga Wagga, NSW 2650, Australia
*
Corresponding author: K. T. Zeleke; Email: kzeleke@csu.edu.au
Rights & Permissions [Opens in a new window]

Abstract

When water and nutrients are not limiting, and pests and disease are effectively controlled, crop growth and yield is determined by weather conditions such as temperature and solar radiation. To determine the relationship between weather indices and crop yield, multiple wheat varieties were sown at two sowing times, for five sowing seasons and at two locations. The following weather indices around the 50% anthesis stage were recorded and analysed: mean temperature (Tmean), maximum temperature (Tmax), number of days with temperature >30°C (T30), vapour pressure deficit (VPD), photosynthetically active radiation, photothermal quotient (PQ) and photothermal quotient corrected for vapour pressure deficit (PQvpd). Overall, for every 1°C rise in temperature, crop yield decreased by 370 kg/ha. For every 1°C rise in temperature, normal sowing window yield decreased by 360 kg/ha while late-sown wheat yield decreased by 640 kg/ha. Correlation analysis was conducted between the weather indices and grain number, grain yield and grain protein. There was a significant positive correlation between PQ and PQvpd and grain number and grain yield. There was a significant negative correlation between Tmean, Tmax, T30 and VPD and grain number and grain yield. Grain protein content showed a positive correlation with maximum air temperature and a negative correlation with the weather indices PQ and PQvpd. PQ and PQvpd can be used to predict grain number and grain yield potential. This study showed that grain number and grain yield predicted using PQ and PQvpd are more reliable than using temperature and radiation individually.

Type
Climate Change and Agriculture Research Paper
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
Copyright © The Author(s), 2023. Published by Cambridge University Press

Introduction

Globally, wheat (Triticum aestivum L.) is the third most widely grown crop, behind only maize and rice (Shiferaw et al., Reference Shiferaw, Smale, Braun, Duveiller, Reynolds and Muricho2013). Australia is the fifth largest wheat exporting country (Qureshi et al., Reference Qureshi, Hanjra and Ward2013). In Australia, wheat is grown mainly in what is commonly called the ‘wheat belt’, a large area of land spanning from South Australia to Central Queensland on the eastern side of the continent plus large areas in the southern and eastern parts of Western Australia. Where nitrogen fertilizer and water are not limiting, and weeds, pests and diseases are controlled, crop yield is limited mainly by incoming solar radiation and the mean air temperature (Kumar et al., Reference Kumar, Rao, Bhavani, Dubey and Singh2016). As a result, agronomic management options are often tailored to maximize adaptation of the crop to the limitations posed by temperature and solar radiation (Sadras et al., Reference Sadras, Vadez, Purushothaman, Lake and Marrou2015). With the rise in global temperatures due to climate change, heat stress is becoming an important limiting factor to crop productivity and food security (Asseng et al., Reference Asseng, Foster and Turner2011). Although significant research has been done on the impact of drought on crop growth and yield, the impact of heat stress due to rising temperatures has received attention only recently (Cohen et al., Reference Cohen, Zandalinas, Huck, Fritschi and Mittler2020).

Global warming has increased the urgency to quantify and manage crop responses to elevated temperatures (Zhao et al., Reference Zhao, Liu, Piao, Wang, Lobell, Huang and Asseng2017). Average atmospheric temperature is expected to increase by 1.8–5.8°C by the end of this century (Pachauri et al., Reference Pachauri, Allen, Barros, Broome, Gramer, Christ, Church, Clarke, Dahe and Dasgupta2014; IPCC Reference Pörtner, Roberts, Tignor, Poloczanska, Mintenbeck, Alegría, Craig, Langsdorf, Löschke, Möller, Okem and Rama2022). In Australia, air temperature has increased by about 1.4°C since the turn of the last century (Ababaei and Chenu, Reference Ababaei and Chenu2020; State of Climate 2020, 2023). Depending on the greenhouse gas emission scenario considered, in Australia, the mean air temperature is predicted to increase by 0.6–1.5°C by 2030 and 2.2–2.5°C by 2070 (Anwar et al., Reference Anwar, Liu, Farquharson, Macadam, Abadi, Finlayson, Wang and Ramilan2015). With the increase in temperature due to climate change, the occurrence of crop heat stress is expected to become more frequent (Cohen et al., Reference Cohen, Zandalinas, Huck, Fritschi and Mittler2020). Global temperature rise has significantly affected wheat yield already (Poudel and Poudel, Reference Poudel and Poudel2020). In general, heat stress in wheat occurs between the temperature range of 32–37°C while temperature above 32°C during the reproductive phase can have a significant negative effect on wheat production (Wahid et al., Reference Wahid, Gelani, Ashraf and Foolad2007; Narayanan et al., Reference Narayanan, Prasad, Fritz, Boyle and Gill2015). Average temperatures higher than 35°C have been found to shorten the grain filling period and decrease wheat yield by 6–51% (Bergkamp et al., Reference Bergkamp, Impa, Asebedo, Fritz and Krishna2018). Lobell and Field (Reference Lobell and Field2007) reported 0.6–8.9% reduction in wheat yield per 1°C rise in air temperature. Globally, wheat production is expected to decrease by up to 6% for each 1°C rise in temperature above the optimum growing season temperature range of 20–25°C (Asseng et al., Reference Asseng, Ewert, Martre, Rotter, Lobell, Cammarano, Kimball, Ottman, Wall and White2015; Ahlawat et al., Reference Ahlawat, Yadav, Kashyap, Khippal and Singh2021).

High temperature affects photosynthetic efficiency, crop phenology, pollen viability and crop water use through vapour pressure deficit (VPD) (Wahid et al., Reference Wahid, Gelani, Ashraf and Foolad2007). The sensitivity of different phenological stages to heat stress differs with heat stress during the reproductive phase (anthesis and grain filling) being the most harmful (Wollenweber et al., Reference Wollenweber, Porter and Schellberg2003). In most wheat-growing regions, including the ‘wheat-belt’ of Australia, temperature ordinarily increases during the growing period as the season progresses. In Australia, such elevated temperatures coincide with the reproductive phase of wheat in September and October (Spring in the southern hemisphere) (Telfer et al., Reference Telfer, Edwards, Kuchel, Reinheimer and Bennet2013). As a result, any heat stress that occurs during the sensitive reproductive stage can lead to significant yield loss (Asseng et al., Reference Asseng, Foster and Turner2011).

Solar radiation is another important environmental factor that alters leaf architecture, light partitioning, photosynthesis and biomass formation (Sandana and Pinochet, Reference Sandana and Pinochet2011). As a result, crop growth and yield are dependent on solar radiation – the higher the availability of solar radiation, the higher the crop yield and biomass. The combined effect of radiation and temperature can be integrated into a photothermal quotient (PQ) index which improves yield and grain weight prediction (Nalley et al., Reference Nalley, Rew and Sayre2009).

To determine suitable planting windows that minimize the impact of environmental stress, it is important to quantify the relationship between weather indices and crop yield components. Although the effect of environmental conditions on wheat yield has been studied extensively under controlled environment conditions (Prasad et al., Reference Prasad, Pisipati, Ristic, Bukovnik and Fritz2008; Zhao et al., Reference Zhao, Tao, Liu, Yang, Zhu, Ding, Zhu, Guo, Zhou and Li2022), a practical way to expose the crop to variable climatic parameters is by sowing different varieties of a crop at different sowing times and at different locations in the field (Martre et al., Reference Martre, Kimball, Ottman, Wall, White, Asseng, Ewert, Cammarano, Maiorano, Aggarwal, Anothai, Basso, Biernath, Challinor, Sanctis, Doltra, Dumont, Fereres, Garcia-Vila, Hoogenboom, Hunt, Izaurralde, Jabloun, Jones, Kassie, Kersebaum, Koehler, Müller, Kumar, Liu, Lobell, Nendel, O'Leary, Olesen, Palosuo, Priesack, Rezaei, Ripoche, Rötter, Semenov, Stöckle, Stratonovitch, Streck, Supit, Tao, Thorburn, Waha, Wang, Wolf, Zhao and Zhu2018). The objective of this study was to determine the relationship between weather indices during the critical reproductive stage and grain number, grain yield and protein content of wheat. In addition, the performance of calculated weather indices (PQ and photothermal quotient corrected for vapour pressure deficit [PQvpd]) for the prediction of grain yield and quality was assessed.

Materials and methods

Study sites and weather data

Crop data for assessing the relationship between weather indices and crop yield were obtained from field trials conducted at two irrigated sites at Leeton Field Station and Wagga Wagga Agricultural Institute (Table 1). The soil at Leeton was a clay Vertosol, while at Wagga Wagga, the soil was sandy clay loam Red Kandosol. Daily weather data of global radiation, minimum and maximum temperature and vapour pressure were sourced from the nearest Bureau of Meteorology weather stations at Yanco Agricultural Institute (−34.62° south, 146.43° east) and Wagga Wagga Agricultural Institute (−35.16° south, 147.46° east) (http://www.bom.gov.au/).

Table 1. Characterization of the soils and long-term (1950–2022) average climate of the two sites

PAWC, plant available water capacity; BD, bulk density; OC, soil organic carbon; GS, growing season (April to October); Temp, mean temperature.

Agronomic practices and crop yield data

The experiments were conducted on a large number of commercial wheat varieties and breeding lines. The details of the field experimental setup (plot size, fertilizer application, irrigation, weed and pest control) were given in Sissons et al. (Reference Sissons, Pleming, Taylor, Emebiri and Collins2017). In summary, the data were derived from 515 wheat germplasm materials used to characterize heat tolerance in field experiments (Collins et al., Reference Collins, Hildebrand, Taylor, Taylor, Pleming, Lohraseb, Shirdelmoghanloo, Erena, Rahman, Taylor, Munoz-Santa, Mather, Heuer, Sissons and Emebiri2017). These were made up of bread wheat and durum lines and consisted of 33 advanced breeding lines obtained from the International Maize and Wheat Improvement Center (CIMMYT), Mexico, 110 released cultivars, 131 landrace materials sourced from heat-prone regions, 61 near-isogenic lines differing at a major gene for heat tolerance (Erena et al., Reference Erena, Lohraseb, Munoz-Santa, Taylor, Emebiri and Collins2021) and 180 recombinant inbred lines used for quantitative trait locus mapping. Altogether, there were 331 bread wheat and 184 durum lines in the germplasm. The objective was to analyse the impact of heat stress on wheat sown at different times as an indicator of the impact of climate change on wheat production. Individual genotypes were not analysed separately.

Crops were sown at two sowing dates each year (a ‘normal’ sowing date in June and a ‘late’ sowing date in August). In Leeton, the crop was sown in 2011 (normal sowing on 1 June and late sowing on 1 August) and in 2015 (normal sowing on 2 June and late sowing on 3 August). In Wagga Wagga, wheat was sown in 2012 (normal sowing on 8 June and late sowing on 8 August), 2018 (normal sowing on 1 June and late sowing on 2 August) and 2019 (normal sowing on 1 June and late sowing on 6 August). The late-sown crop in each case is expected to experience more heat stress during the reproductive (anthesis and grain filling) stage. In each trial, the dates of sowing, flowering and maturity were recorded, along with grain yield, and 1000 grain weight.

Weather indices

Temperature and photosynthetically active radiation

Daily maximum and minimum temperatures (°C) and global radiation (MJ/m2/d) for each site were obtained from the closest Australian Bureau of Meteorology weather stations (http://www.bom.gov.au/). Maximum temperature data were used to calculate the number of hot days (T max > 30°C). Photosynthetically active radiation (PAR) was obtained by multiplying global solar radiation by 0.47 (Pinker and Laszlo, Reference Pinker and Laszlo1992).

Vapour pressure deficit

The VPD (kPa) was calculated as the difference between the actual air vapour pressure, VPact and the saturated vapour pressure, VPsat (Equation (1)). VPsat was estimated for a temperature Ti, either maximum (T max) or minimum (T min) (Dreccer et al., Reference Dreccer, Fainges, Whish, Ogbonnaya and Sadras2018). Finally, VPsat was calculated as the weighted average of vapour pressure at T max and T min (Jeffrey et al., Reference Jeffrey, Carter, Moodie and Beswick2001) (Equation (2)).

(1)$${\rm VPD} = 0.75\;\left[{0.6107 \times e^{\left({{{17.4 \times T_{{\rm max}}} \over {239 + T_{{\rm max}}}}} \right)}-0.6107 \times e^{\left({{{17.4 \times T_{{\rm min}}} \over {239 + T_{{\rm min}}}}} \right)}} \right]$$

PQ and PQvpd

Heat stress during the reproductive stage (anthesis and grain filling) has a significant effect on grain yield and quality. Some previous studies have used either 30 or 45 days before to 0 days after 50% anthesis, or 20 days before to 10 days after anthesis as a critical period for heat stress analysis. In northwest Mexico, Fischer (Reference Fischer1985) reported that there is a strong relationship between the PQ value calculated from 30 days before to 0 days after 50% anthesis. However, further studies showed that the critical period spans only about 20 days before to 10 days after anthesis (Ortiz-Monasterio et al., Reference Ortiz-Monasterio, Dhillon and Fischer1994; Abbate et al., Reference Abbate, Andrade and Culot1995). In this work, both indices were calculated as the average for the period 20 days before to 10 days after anthesis.

PQ was calculated as the ratio between PAR and mean temperature for the critical period with a base temperature assumed as 0°C (Fischer, Reference Fischer1985; Soltani and Sinclair, Reference Soltani and Sinclair2011).

(2)$${\rm PQ} = \displaystyle{{\mathop \sum \nolimits_{{\rm start}}^{{\rm end}} {\rm PAR}} \over {{\bar{T}}_{{\rm start}-{\rm end}}}}$$

where PQ is the cumulative PQ over a given period, the critical period around anthesis (MJ/m2/°C), PAR is the daily photosynthetically active radiation (MJ/m2/d) and $\bar{T}_{{\rm start}-{\rm end}}$ is the mean temperature over the given period (oC).

Mean daily PQ is then calculated by dividing the above cumulative PQ by the number of days (30 days, in this case).

A PQvpd (MJ/m2/°C/kPa) was calculated as the ratio between PQ and mean VPD during the critical period (Rodriguez and Sadras, Reference Rodriguez and Sadras2007).

(3)$${\rm P}{\rm Q}_{{\rm vpd}} = \displaystyle{{\mathop \sum \nolimits_{{\rm start}}^{{\rm end}} {\rm PAR}} \over {{\bar{T}}_{{\rm start}-{\rm end}} \times \;{\overline {{\rm VPD}} }_{{\rm start}-{\rm end}}}}$$

where $\overline {{\rm VPD}} _{{\rm start}-{\rm end}}$ is the mean vapour pressure deficit over the critical period around anthesis (kPa). Mean daily PQvpd is then calculated by dividing the above cumulative PQvpd by the number of days (30 days, in this case).

Data analysis

The weather and crop data were analysed using R (R Core Team, 2022). Linear regression analysis was performed, and Pearson's correlation coefficient was used to quantify the effect of temperature, PAR, VPD, PQ and PQvpd on yield and yield components. The statistical significance of the correlations was determined using P-levels. For this purpose, daily indices during the critical stage were averaged for all the cultivars and years of experimentation. Data manipulation and presentation utilized various ‘tidyverse’ R packages (Wickham et al., Reference Wickham, Averick, Bryan, Chang, McGowan, François, Grolemund, Hayes, Henry, Hester, Kuhn, Pedersen, Miller, Bache, Müller, Ooms, Robinson, Seidel, Spinu, Takahashi, Vaughan, Wilke, Woo and Yutani2019).

Results

Summary of weather indices and crop yield and quality

Overall mean of weather indices and crop yield components is given in Table 2. The number of hot days (>30°C) was greater during the second sowing (as expected). Temperature and VPD were higher for the late-sown crop. However, PQ and PQvpd decreased during the second sowing. Compared to wheat sown during the normal sowing period, late-sown wheat had 44 and 40% lower yields, respectively, for Leeton and Wagga Wagga. Grain size was also smaller for the late-sown wheat while grain protein increased during the second sowing. Maximum values of grain numbers were six times greater than the minimum values, whereas maximum grain weights were only twice as large as the minimum values. This indicates that grain number contributed the most to overall grain yield variation.

Table 2. Mean weather indices and yield components for wheat sown in Leeton and Wagga Wagga at two sowing times: normal sowing time in June (ST1) and late sowing time in August (ST2). The range of the values is shown in parentheses

TGW, 1000 grains weight; NG, number of grains per m2; Prot, grain protein; T30, number of days with temperature >30°C; T mean, mean temperature; PAR, photosynthetically active radiation; VPD, vapour pressure deficit; PQ, photothermal quotient; PQvpd, photothermal quotient corrected for vapour pressure deficit; T max, maximum temperature.

Effect of temperature, solar radiation and VPD on grain number and grain yield

Tables 3–5 show the correlation between weather parameters and wheat yield components. Both grain number and grain yield are negatively correlated with mean maximum temperature T max, temperature above 30°C (T30), PAR and VPD. The only exception is PAR at Wagga Wagga which is positively correlated with grain number and grain yield. Grain protein is, however, positively correlated with each of these weather parameters. The association between yield and yield components and weather parameters is higher for late-sown wheat compared to the crop sown in the normal sowing window, presumably due to the higher incidence of abiotic stress.

Table 3. Correlation coefficients of weather indices and wheat yield components for combined Leeton and Wagga Wagga data

Non-significant correlations (at P = 1%) are indicated by bold italics.

TGW, 1000 grains weight; NG, number of grains per m2; Prot, grain protein; T30, number of days with temperature >30°C; T mean, mean temperature; PAR, photosynthetically active radiation; VPD, vapour pressure deficit; PQ, photothermal quotient; PQvpd, photothermal quotient corrected for vapour pressure deficit; T max, maximum temperature.

Table 4. Correlation coefficients of weather indices and wheat yield components for first sowing and second sowing (ST1 and ST2) combined, first sowing (ST1) and second sowing (ST2), respectively, at Leeton

Non-significant correlations (at P = 1%) are indicated by bold italics.

TGW, 1000 grains weight; NG, number of grains per m2; Prot, grain protein; T30, number of days with temperature >30°C; T mean, mean temperature; PAR, photosynthetically active radiation; VPD, vapour pressure deficit; PQ, photothermal quotient; PQvpd, photothermal quotient corrected for vapour pressure deficit; T max, maximum temperature.

Table 5. Correlation coefficients of weather indices and wheat yield components for first sowing and second sowing (ST1 and ST2) combined, first sowing (ST1) and second sowing (ST2), respectively, at Wagga Wagga

Non-significant correlations (at P = 1%) are indicated by bold italics.

TGW, 1000 grains weight; NG, number of grains per m2; Prot, grain protein; T30, number of days with temperature >30°C; T mean, mean temperature; PAR, photosynthetically active radiation; VPD, vapour pressure deficit; PQ, photothermal quotient; PQvpd, photothermal quotient corrected for vapour pressure deficit; T max, maximum temperature.

Figure 1 shows the linear relationship between the mean maximum temperature during the critical stage and grain yield. Late sowing exposed the crop to more hot days. Late-sown crops grew under higher maximum temperatures compared to crops sown during the normal sowing window. As the temperature increased, the crop yield decreased. The overall mean result (Fig. 1(g)) shows that for every 1°C rise in temperature, crop yield decreases by 370 kg/ha. In Leeton, for every 1°C rise in temperature, grain yield of wheat sown in the normal sowing window decreased by 360 kg/ha while the late-sown crop yield reduced by 640 kg/ha. The overall impact is higher in Leeton (470 kg/ha) than in Wagga Wagga (310 kg/ha). As the mean temperature during the critical period increases, both grain yield and grain number decrease (Tables 3–5). Temperature explained 51 and 43% of the yield and grain number variation, respectively.

Figure 1. Regression analysis of mean maximum temperature during the critical development stage of wheat and grain yield. Wheat was sown at two sowing dates: normal sowing window (Sowing 1) and late (Sowing 2) in Leeton and Wagga Wagga.

Figure 2 shows the impact of the number of days with temperature above 30°C (T30) during the 30 days around anthesis (20 days before to 10 days after anthesis) on grain yield. Wheat yield decreases as the number of days with temperature above the threshold increases. When all the data are considered, for each day above the threshold temperature, crop yield decreases by 231 kg/ha for every day with T > 30°C (Fig. 2(g)). The decrease is higher for sowing time 2 (ST2, August) compared to sowing time 1 (ST1, June). For Leeton, for example, the decrease is 300 and 128 kg/ha for ST1 and ST2, respectively.

Figure 2. Regression analysis of the number of days with temperature above 30°C during the critical development stage of wheat and grain yield. Wheat was sown at two sowing dates: normal sowing window (Sowing 1) and late (Sowing 2) in Leeton and Wagga Wagga.

Figure 3 presents the effect of VPD on wheat productivity. About 57% of the yield variation is explained by VPD. As expected, as VPD increases, crop yield decreases. This is especially pronounced for the second sowing date. Overall results show that for every 1 kPa increase in VPD, crop yield decreases by 2.6 t/ha. The yield loss is higher in the late-sown wheat; with 2.57 t/ha for the late-sown crop compared to 2.11 t/ha for the crop sown in the normal crop sowing window. The impact is higher for the crop sown at Leeton compared to the crop sown at Wagga Wagga (4.66 t/ha v. 2.11 t/ha). Compared to temperature and VPD, PAR has only little impact on grain number and yield (data not shown here). This is probably due to the ample radiation during the reproductive (anthesis and grain filling) stage of wheat and radiation not being a limiting factor. Generally, compared to grain number (hence grain yield), grain size was only slightly affected by temperature, VPD and PAR.

Figure 3. Regression analysis of the vapour pressure deficits (VPD) during the critical development stage of wheat and grain yield. Wheat was sown at two sowing dates: normal sowing window (Sowing 1) and late (Sowing 2) in Leeton and Wagga Wagga.

Figure 4 shows the effect of maximum temperature on the grain number for wheat sown at Leeton and Wagga Wagga during normal sowing window and sown late, respectively. Similar to the trend observed for grain yield, grain number decreases with the increase in mean maximum temperature. Overall results show that for every 1°C rise in maximum air temperature, the number of grains drop by 935 grains/m2. The drop in grain numbers is higher for late-sown wheat compared to the crop sown during the normal sowing window (1320/m2 v. 450/m2). Although the result for grain weight is somehow mixed, generally there is a decreasing trend of grain weight.

Figure 4. Regression analysis of mean maximum temperature and grain number per square metre during the critical development stage. Wheat was sown at two sowing dates: (normal sowing window (Sowing 1) and late (Sowing 2) in Leeton and Wagga Wagga.

PQ and PQvpd as predictors of grain yield

Figures 5 and 6 show the linear regression of grain yields v. PQ and PQvpd, respectively. Both grain number and grain yield increase with increasing PQ and PQvpd. PQ integrates PAR and mean temperature during the critical crop development stage to explain the effect of non-stressful thermal effects on crop development, canopy size and seed set. PQ ranged from 0.50 to 0.80 MJ/m2/°C/d. Considering the whole data set for Leeton and Wagga Wagga, 52% of grain yield variation can be explained by PQ variation (Fig. 5). The photothermal quotient normalized by VPD (PQvpd) accounted for 60% of the variation in grain yield (Fig. 6).

Figure 5. Regression analysis of the photothermal quotient (PQ) during the critical development stage of wheat and grain yield. Wheat was sown at two sowing dates: (normal sowing window (Sowing 1) and late (Sowing 2) in Leeton and Wagga Wagga.

Figure 6. Regression analysis of the photothermal quotient corrected by vapour pressure deficit (PQvpd) during the critical development stage of wheat and grain yield. Wheat was sown at two sowing dates: (normal sowing window (Sowing 1) and late (Sowing 2) in Leeton and Wagga Wagga.

Impact of weather indices on grain protein

Tables 3–5 show that as maximum temperature, temperature above 30°C threshold and VPD increase, grain protein content increases. Figure 7 shows that mean maximum temperature explains about 30% of grain protein content variation.

Figure 7. Regression analysis of the maximum temperature during the critical development stage of wheat and grain protein. Wheat was sown at two sowing dates: (normal sowing window (Sowing 1) and late (Sowing 2) in Leeton and Wagga Wagga.

Discussion

Wheat grain yield potential is determined by grain number and grain weight. When water and nutrients are not limiting, these two yield components are largely determined by solar radiation and air temperature. Wheat performs best when grown within the mean temperature range of 12–22°C during the growing season (Farooq et al., Reference Farooq, Bramley, Palta and Siddique2011). However, in the Australian ‘wheat belt’, the daily maximum temperatures during the crop reproductive stage are frequently in a higher range which can accelerate the development process and reduces the duration of grain filling and grain weight (Kumar et al., Reference Kumar, Rao, Bhavani, Dubey and Singh2016). As a result, breeding for heat tolerance would be desirable for wheat grown in the Australian ‘wheat belt’, where mean air temperatures during the reproductive stage are above the optimum.

Crop productivity is becoming limited due to heat stresses resulting from rising atmospheric temperatures (Vollenweider and Gunthardt-Georg, Reference Vollenweider and Gunthardt-Georg2005). In the Australian ‘wheat belt’, heat shocks due to high temperatures (>30°C) are common during the crop reproductive stages. Impaired photosynthesis and reproductive damage at high temperature have been demonstrated in controlled environments (Wang et al., Reference Wang, Hou, Lu, Wu, Gong, Liu, Wang, Sun, Vierling and Xu2018). Short periods, as short as one day, of high temperatures (>30°C) directly affect the crop by reducing photosynthesis and/or causing sterility or reproductive failure, resulting in reduced grain number (Talukder et al., Reference Talukder, McDonald and Gill2014; Mirosavljevic et al., Reference Mirosavljevic, Mikic, Zupunski, Spika, Trkulja, Ottosen, Zhou and Abdelhakim2021). The number of stressful temperature days above 30°C increases in frequency later in the season, negatively affecting grain filling, grain weight and grain yield (Savin and Slafer, Reference Savin and Slafer1991). Hawker and Jenner (Reference Hawker and Jenner1993) reported that the grain weight of wheat exposed to maximum temperatures of 35°C for four days was reduced by 14–20%. Yield loss per °C at Leeton is 50% higher than that of Wagga Wagga in indicating that the impact of climate change is higher in drier environments (Sreeparvathy and Srinivas, Reference Sreeparvathy and Srinivas2022).

Stressful and non-stressful atmospheric temperatures, PQ and PQvpd were identified to be reliable weather indices for wheat yield prediction. PQ normalized by VPD (PQvpd) was found to be a better predictor of wheat yield potential than PQ as it integrates more weather data that affects crop growth. Since radiation use efficiency decreases as VPD and maximum temperature increase, there is a better correlation between PQvpd and grain number and yield in comparison to PQ (Lazaro and Abbate, Reference Lazaro and Abbate2012). PQvpd captures the detrimental effect of high VPD and high temperature on photosynthesis and reproduction (Sadras et al., Reference Sadras, Vadez, Purushothaman, Lake and Marrou2015). Solar radiation and temperature affect plant growth and development differently (Nix, Reference Nix1976). A higher PQ indicates high yield potential as radiation increases growth, while lower temperature increases the length of the crop phenological stages. High solar radiation during the crop reproductive stage increases photosynthesis and yield. On the other hand, high temperature around the same period shortens the duration of the reproductive stage and reduces yield. Mean PQ around anthesis (20 days before to 10 days after anthesis) was found to be a good indicator of grain number and grain yield. Ortiz-Monasterio et al. (Reference Ortiz-Monasterio, Dhillon and Fischer1994) reported that the PQ value 20 days before to 10 days after anthesis predicted grain yield reasonably accurately.

Grain yield is determined by grain number and grain weight. Grain number accounts for much of the variation in yield between crops and environments. Given the strong correlation between grain number and yield, the association between yield and PQ and PQvpd was also strong, while grain weight is relatively stable for a given crop variety (Fischer, Reference Fischer1985). Since grain number is determined in the period immediately before anthesis, there is a strong association between grain number and the PQ and PQvpd around anthesis (20 days before and 10 days after).

Global temperature rise is increasing the atmospheric saturation vapour pressure as saturation vapour pressure is a function of air temperature (Lawrence, Reference Lawrence2005). As a result, since actual vapour pressure has not been increasing at the same rate, VPD is rising (Grossiord et al., Reference Grossiord, Buckley, Cernusak, Novick, Poulter, Siegwolf, Sperry and McDowell2020). In most global wheat-growing regions, including the Australian ‘wheat belt’, VPD increases during the reproductive (anthesis and grain filling) stage of the crop. The high VPD causes plants to close their stomata, reduce transpiration rate and reduce photosynthesis (Franks et al., Reference Franks, Cowan and Farquhar1997).

In annual crops, grain yield is determined mainly by grain number which depends on the conditions that occur before anthesis, while grain size is determined by the environmental conditions that occur after anthesis (Ortiz-Monasterio et al., Reference Ortiz-Monasterio, Dhillon and Fischer1994). Grain number, rather than grain size, is more sensitive and responsive to high temperatures at anthesis (Fernie et al., Reference Fernie, Tan, Liu, Ullah and Khoddami2022). Narayanan et al. (Reference Narayanan, Prasad, Fritz, Boyle and Gill2015) reported that grain number was reduced by 17% for wheat exposed to 7-day heat stress at anthesis.

Late-sown wheat has a lower yield but higher protein content. Grain protein content was positively affected by air temperature during the grain filling period. Zhao et al. (Reference Zhao, Tao, Liu, Yang, Zhu, Ding, Zhu, Guo, Zhou and Li2022) found that as the maximum temperature during the grain filling period increases, grain protein content increases and grain size decreases as grain protein content is inversely related to grain weight. Heat stress during grain development had adverse effects on starch biosynthesis (reduces grain weight) and increases protein content (Wang et al., Reference Wang, Hou, Lu, Wu, Gong, Liu, Wang, Sun, Vierling and Xu2018). From tests conducted on several genotypes, Barutcular et al. (Reference Barutcular, Yildirim, Koc, Dizlek, Akinci, El Sabagh, Saneoka, Ueda, Islam and Toptas2016) found that protein content increases by an average of 39.6% at a temperature of 26.3°C. In winter wheat cultivars, Liu et al. (Reference Liu, Asseng, Liu, Tang, Cao and Zhu2016) found that grain protein content increased by 0.80% for every 1°C above 30°C after anthesis. Although heat stress can affect any wheat growth stage, it's impact is most significant if it occurs during the reproductive stage. On average, as the sowing time is delayed, the crop is exposed to higher daily maximum temperatures and more hot days. Agronomic management such as early sowing can be used to minimize the coincidence of reproductive crop development stage and periods of climatic stresses such as heat and drought. Since grain yield is strongly correlated with grain number and grain number is mainly determined before and during anthesis, the critical period that determines yield is anthesis.

Conclusions

Linear regression analysis showed that weather indices account for much of the variability in grain number and yield. Grain number is the most important component of yield and is strongly correlated with PQ for wheat grown with no water and nutrient limitation. PQ and PQvpd are better predictors of wheat grain yield and quality than their components (temperature, radiation and VPD) alone. Overall, PQvpd was the better indicator of yield potential. Therefore, PQ and PQvpd can be used to predict or explain grain productivity and identify sowing times and growing regions that maximize grain yield potential. Varieties released several years apart can have marked differences in the number of grains and grain yield due to genetic improvement. However, in this study, genetic variability in heat tolerance for both grain yield and quality were not specifically considered as we were more interested in the overall responses for all the cultivars. The variety-by-environment aspects of this work will be investigated further.

Acknowledgements

We acknowledge the contributions of Dr Nicholas Collins (School of Agriculture Food and Wine, The University of Adelaide, Adelaide, SA, Australia) who supervised these projects and thank all the technical staff involved in the field experiments.

Authors’ contribution

Ketema T. Zeleke contributed to the conceptualization, investigation, methodology, writing – original draft and writing – review and editing. Muhuddin Rajin Anwar contributed to the conceptualization, data curation, formal analysis, investigation, visualization and writing – review and editing. Livinus Emebiri contributed to the conceptualization, funding acquisition, project administration, resources, investigation and writing – review and editing. David J. Luckett contributed to the software, investigation, visualization and writing – review and editing.

Funding statement

The data used for this paper were derived from research projects funded by the Grains Research and Development Corporation (GRDC) under project UA00123 and UA00147.

Competing interests

None.

Ethical standards

Not applicable.

References

Ababaei, B and Chenu, K (2020) Heat shocks increasingly impede grain filling but have little effect on grain setting across the Australian wheatbelt. Agricultural and Forrest Meteorology 284, 107889.CrossRefGoogle Scholar
Abbate, P, Andrade, F and Culot, J (1995) The effects of radiation and nitrogen on the number of grains in wheat. The Journal of Agricultural Science 124, 351360.CrossRefGoogle Scholar
Ahlawat, OP, Yadav, D, Kashyap, PL, Khippal, A and Singh, G (2021) Wheat endophytes and their potential role in managing abiotic stress under changing climate. Journal of Applied Microbiology 132, 25012520.CrossRefGoogle ScholarPubMed
Anwar, MR, Liu, DL, Farquharson, R, Macadam, I, Abadi, A, Finlayson, J, Wang, B and Ramilan, T (2015) Climate change impacts on phenology and yields of five broadacre crops at four climatologically distinct locations in Australia. Agricultural Systems 132, 133144.CrossRefGoogle Scholar
Asseng, S, Foster, I and Turner, NC (2011) The impact of temperature variability on wheat yields. Global Change Biology 17, 9971012.CrossRefGoogle Scholar
Asseng, S, Ewert, F, Martre, P, Rotter, RP, Lobell, DB, Cammarano, D, Kimball, BA, Ottman, MJ, Wall, G and White, JW (2015) Rising temperatures reduce global wheat production. Nature Climate Change 5, 43147.CrossRefGoogle Scholar
Barutcular, C, Yildirim, M, Koc, M, Dizlek, H, Akinci, C, El Sabagh, A, Saneoka, H, Ueda, A, Islam, M and Toptas, I (2016) Quality traits performance of bread wheat genotypes under drought and heat stress conditions. Fresenius Environmental Bulletin 25, 61596165.Google Scholar
Bergkamp, B, Impa, SM, Asebedo, AR, Fritz, AK and Krishna, JSV (2018) Prominent winter wheat varieties response to post-flowering heat stress under controlled chambers and field based heat tents. Field Crops Research 222, 143152.CrossRefGoogle Scholar
Cohen, I, Zandalinas, SI, Huck, C, Fritschi, FB and Mittler, R (2020) Meta-analysis of drought and heat stress combination impact on crop yield and yield components. Physiologia Plantrarum 171, 6676.CrossRefGoogle ScholarPubMed
Collins, NC, Hildebrand, S, Taylor, K, Taylor, H, Pleming, D, Lohraseb, I, Shirdelmoghanloo, H, Erena, M, Rahman, M, Taylor, J, Munoz-Santa, S, Mather, D, Heuer, S, Sissons, M and Emebiri, L (2017) Understanding Heat Impacts on Wheat to Breed Future Tolerance. Available at https://grdc.com.au/resources-and-publications/grdc-update-papers/tab-content/ (accessed 11 February 2022).Google Scholar
Dreccer, MF, Fainges, J, Whish, J, Ogbonnaya, FC and Sadras, VO (2018) Comparison of sensitive stages of wheat, barley, canola, chickpea and field pea to temperature and water stress across Australia. Agricultural and Forest Meteorology 248, 275294.CrossRefGoogle Scholar
Erena, MF, Lohraseb, I, Munoz-Santa, I, Taylor, JD, Emebiri, LC and Collins, NC (2021) The WtmsDW locus on wheat chromosome 2B controls major natural variation for floret sterility responses to heat stress at booting stage. Frontiers in Plant Science 12, 376.CrossRefGoogle ScholarPubMed
Farooq, M, Bramley, H, Palta, JA and Siddique, KHM (2011) Heat stress in wheat during reproductive and grain-filling phases. Critical Reviews Plant in Sciences 30, 491507.CrossRefGoogle Scholar
Fernie, E, Tan, DKY, Liu, SY, Ullah, N and Khoddami, A (2022) Post-anthesis heat influences grain yield, physical and nutritional quality in wheat: review. Agriculture 12, 886.CrossRefGoogle Scholar
Fischer, RA (1985) Number of grains in wheat crops and the influence of solar radiation and temperature. Journal of Agricultural Science 105, 447461.CrossRefGoogle Scholar
Franks, PJ, Cowan, IR and Farquhar, GD (1997) The apparent feedforward response of stomata to air vapour pressure deficit: information revealed by different experimental procedures with two rainforest trees. Plant, Cell and Environment 20, 142145.CrossRefGoogle Scholar
Grossiord, C, Buckley, TN, Cernusak, LA, Novick, KA, Poulter, B, Siegwolf, RTW, Sperry, JS and McDowell, NG (2020) Plant responses to rising vapour pressure deficit. New Phytologist 226, 11501566.CrossRefGoogle Scholar
Hawker, JS and Jenner, CF (1993) High temperature affects the activity of enzymes in the committed pathway of starch synthesis in developing wheat endosperm. Australian Journal of Plant Physiology 20, 197209.Google Scholar
IPCC (2022) Climate Change 2022: Impacts, Adaptation and Vulnerability. Contribution of Working Group II to the Sixth Assessment Report of the Intergovernmental Panel on Climate Change. [Pörtner, HO, Roberts, DC, Tignor, M, Poloczanska, ES, Mintenbeck, K, Alegría, A, Craig, M, Langsdorf, S, Löschke, S, Möller, V, Okem, A and Rama, B (eds).] Cambridge and New York: Cambridge University Press, p. 3056. https://doi.org/10.1017/9781009325844.Google Scholar
Jeffrey, SJ, Carter, JO, Moodie, KB and Beswick, AR (2001) Using spatial interpolation to construct a comprehensive archive of Australian climate data. Environmental Modelling Software 16, 309330.CrossRefGoogle Scholar
Kumar, P, Rao, VUM, Bhavani, O, Dubey, AP and Singh, CB (2016) Effect of temperature and photothermal quotient on the yield components of wheat (Triticum aestivum L.) in Indo-Gangetic plains of India. Experimental Agriculture 52, 1435.CrossRefGoogle Scholar
Lawrence, MG (2005) The relationship between relative humidity and the dewpoint temperature in moist air – a simple conversion and applications. Bulletin of the American Meteorological Society 86, 225233.CrossRefGoogle Scholar
Lazaro, L and Abbate, PE (2012) Cultivar effects on relationship between grain number and photothermal quotient or spike dry weight in wheat. Journal of Agricultural Science 150, 442459.CrossRefGoogle Scholar
Liu, B, Asseng, S, Liu, L, Tang, L, Cao, W and Zhu, Y (2016) Testing the responses of four wheatcrop models to heat stress at anthesis and grain filling. Global Change Biology 22, 18901903.CrossRefGoogle ScholarPubMed
Lobell, DB and Field, CB (2007) Global scale climate–crop yield relationships and the impact of recent warming. Environmental Research Letters 2, 17.CrossRefGoogle Scholar
Martre, P, Kimball, BA, Ottman, MJ, Wall, GW, White, JW, Asseng, S, Ewert, F, Cammarano, D, Maiorano, A, Aggarwal, PK, Anothai, J, Basso, B, Biernath, C, Challinor, AJ, Sanctis, GD, Doltra, J, Dumont, B, Fereres, E, Garcia-Vila, M, Hoogenboom, SG, Hunt, LA, Izaurralde, RC, Jabloun, M, Jones, CD, Kassie, BT, Kersebaum, KC, Koehler, AK, Müller, C, Kumar, SN, Liu, B, Lobell, DB, Nendel, C, O'Leary, G, Olesen, JE, Palosuo, T, Priesack, E, Rezaei, EE, Ripoche, D, Rötter, RP, Semenov, MA, Stöckle, C, Stratonovitch, P, Streck, T, Supit, I, Tao, F, Thorburn, P, Waha, K, Wang, E, Wolf, J, Zhao, Z and Zhu, Y (2018) The Hot Serial Cereal Experiment for modeling wheat response to temperature: field experiments and AgMIP-Wheat multi-model simulations. Open Data Journal for Agricultural Research 4, 2834.CrossRefGoogle Scholar
Mirosavljevic, M, Mikic, S, Zupunski, V, Spika, A, Trkulja, D, Ottosen, CO, Zhou, R and Abdelhakim, L (2021) Effects of high temperature during anthesis and grain filling on physiological characteristics of winter wheat cultivars. Journal of Agronomy and Crop Science 207, 823832.CrossRefGoogle Scholar
Nalley, LL, Rew, PB and Sayre, K (2009) Photothermal quotient specifications to improve wheat cultivar yield component models. Agronomy Journal 101, 556563.CrossRefGoogle Scholar
Narayanan, S, Prasad, P, Fritz, A, Boyle, D and Gill, B (2015) Impact of high night-time and high daytime temperature stress on winter wheat. Journal of Agronomy and Crop Science 201, 206218.CrossRefGoogle Scholar
Nix, HA (1976) Climate and crop productivity in Australia. In Climate and Rice. Philippines: International Rice Research Institute, pp. 495506.Google Scholar
Ortiz-Monasterio, R, Dhillon, S and Fischer, R (1994) Date of sowing effects on grain yield and yield components of irrigated spring wheat cultivars and relationships with radiation and temperature in Ludhiana, India. Field Crops Research 37, 169184.CrossRefGoogle Scholar
Pachauri, RK, Allen, MR, Barros, VR, Broome, J, Gramer, W, Christ, R, Church, JA, Clarke, L, Dahe, Q and Dasgupta, P (2014) Climate Change 2014: Synthesis Report. Contribution of Working Groups I, II and III to the Fifth Assessment Report of the Intergovernmental Panel on Climate Change. Geneva, Switzerland: Intergovernmental Panel on Climate Change. Available at https://www.ipcc.ch/report/ar5/syr/.Google Scholar
Pinker, RT and Laszlo, I (1992) Global distribution of photosynthetically active radiation as observed from satellites. Journal of Climate 5, 5665.2.0.CO;2>CrossRefGoogle Scholar
Poudel, PB and Poudel, MR (2020) Heat stress effects and tolerance in wheat: a review. Journal of Biology and Today's World 9, 217.Google Scholar
Prasad, PVV, Pisipati, SR, Ristic, Z, Bukovnik, U and Fritz, AK (2008) Impact of nighttime temperature on physiology and growth of spring wheat. Crop Science 48, 23722380.CrossRefGoogle Scholar
Qureshi, EM, Hanjra, MA and Ward, J (2013) Impact of water scarcity in Australia on global food security in an era of climate change. Food Policy 38, 136145.CrossRefGoogle Scholar
R Core Team (2022) R: A Language and Environment for Statistical Computing. Vienna, Austria. Available at http://www.R-project.org.Google Scholar
Rodriguez, D and Sadras, VO (2007) The limit to wheat water use efficiency in eastern Australia. I. Gradients in the radiation environment and atmospheric demand. Australian Journal of Agricultural Research 58, 287302.CrossRefGoogle Scholar
Sadras, VO, Vadez, V, Purushothaman, R, Lake, L and Marrou, H (2015) Unscrambling confounded effects of sowing date trials to screen for crop adaptation to high temperature. Field Crops Research 177, 18.CrossRefGoogle Scholar
Sandana, P and Pinochet, D (2011) Ecophysiological determinants of biomass and grain yield of wheat under P deficiency. Field Crops Research 120, 311319.CrossRefGoogle Scholar
Savin, R and Slafer, G (1991) Shading effects on yield of an Argentinean wheat cultivar. Journal of Agricultural Science 116, 17.CrossRefGoogle Scholar
Shiferaw, B, Smale, M, Braun, H-J, Duveiller, E, Reynolds, M and Muricho, G (2013) Crops that feed the world 10. Past successes and future challenges to the role played by wheat in global food security. Food Security 5, 291317.CrossRefGoogle Scholar
Sissons, M, Pleming, D, Taylor, JD, Emebiri, L and Collins, NC (2017) Effects of heat exposure from late sowing on the agronomic and technological quality of tetraploid wheat. Cereal Chemistry 95, 274287.CrossRefGoogle Scholar
Soltani, A and Sinclair, TR (2011) A simple model for chickpea development, growth and yield. Field Crops Research 124, 252260.CrossRefGoogle Scholar
Sreeparvathy, V and Srinivas, VV (2022) Global assessment of spatiotemporal variability of wet, normal and dry conditions using multiscale entropy-based approach. Scientific Reports 12, 9667.CrossRefGoogle ScholarPubMed
State of the Climate 2020 (2023) Available at www.bom.gov.au (accessed 17 March 2023).Google Scholar
Talukder, ASMHM, McDonald, GK and Gill, GS (2014) Effect of short-term heat stress prior to flowering and early grain set on the grain yield of wheat. Field Crops Research 160, 5463.CrossRefGoogle Scholar
Telfer, P, Edwards, J, Kuchel, H, Reinheimer, J and Bennet, D (2013) Heat Stress Tolerance in Heat. Canberra: Grains Research and Development Corporation. Available at https://grdc.com.au/resources-and-publications/grdc-update-papers/tab-content/grdc-update-papers/2013/02/heat-stress-tolerance-of-wheat.Google Scholar
Vollenweider, P and Gunthardt-Georg, M (2005) Diagnosis of abiotic and biotic stress factors using the visible symptoms in foliage. Environmental Pollution 137, 455–165.CrossRefGoogle ScholarPubMed
Wahid, A, Gelani, S, Ashraf, M and Foolad, MR (2007) Heat tolerance in plants: an overview. Environmental and Experimental Botany 61, 199223.CrossRefGoogle Scholar
Wang, X, Hou, L, Lu, Y, Wu, B, Gong, X, Liu, M, Wang, J, Sun, Q, Vierling, E and Xu, S (2018) Metabolic adaptation of wheat grain contributes to a stable filling rate under heat stress. Journal of Experimental Botany 69, 55315545.Google ScholarPubMed
Wickham, H, Averick, M, Bryan, J, Chang, W, McGowan, LD, François, R, Grolemund, G, Hayes, A, Henry, L, Hester, J, Kuhn, M, Pedersen, TL, Miller, E, Bache, SM, Müller, K, Ooms, J, Robinson, D., Seidel, DP, Spinu, V, Takahashi, K, Vaughan, D, Wilke, C, Woo, K and Yutani, H (2019) Welcome to the tidyverse. Journal of Open Source Software 43, 1686.CrossRefGoogle Scholar
Wollenweber, B, Porter, JR and Schellberg, J (2003) Lack of interaction between extreme high-temperature events at vegetative and reproductive growth stages in wheat. Journal of Agronomy and Crop Science 189, 142150.CrossRefGoogle Scholar
Zhao, C, Liu, C, Piao, S, Wang, X, Lobell, DB, Huang, Y and Asseng, S (2017) The increase in temperature reduces the overall yield of the main crops in four independent estimates. Proceedings of the National Academy of Science of USA 114, 93269331.CrossRefGoogle Scholar
Zhao, K, Tao, Y, Liu, M, Yang, D, Zhu, M, Ding, J, Zhu, X, Guo, W, Zhou, G and Li, C (2022) Does temporary heat stress or low temperature stress similarly affect yield, starch, and protein of winter wheat grain during grain filling? Journal of Cereal Science 103, 103408.CrossRefGoogle Scholar
Figure 0

Table 1. Characterization of the soils and long-term (1950–2022) average climate of the two sites

Figure 1

Table 2. Mean weather indices and yield components for wheat sown in Leeton and Wagga Wagga at two sowing times: normal sowing time in June (ST1) and late sowing time in August (ST2). The range of the values is shown in parentheses

Figure 2

Table 3. Correlation coefficients of weather indices and wheat yield components for combined Leeton and Wagga Wagga data

Figure 3

Table 4. Correlation coefficients of weather indices and wheat yield components for first sowing and second sowing (ST1 and ST2) combined, first sowing (ST1) and second sowing (ST2), respectively, at Leeton

Figure 4

Table 5. Correlation coefficients of weather indices and wheat yield components for first sowing and second sowing (ST1 and ST2) combined, first sowing (ST1) and second sowing (ST2), respectively, at Wagga Wagga

Figure 5

Figure 1. Regression analysis of mean maximum temperature during the critical development stage of wheat and grain yield. Wheat was sown at two sowing dates: normal sowing window (Sowing 1) and late (Sowing 2) in Leeton and Wagga Wagga.

Figure 6

Figure 2. Regression analysis of the number of days with temperature above 30°C during the critical development stage of wheat and grain yield. Wheat was sown at two sowing dates: normal sowing window (Sowing 1) and late (Sowing 2) in Leeton and Wagga Wagga.

Figure 7

Figure 3. Regression analysis of the vapour pressure deficits (VPD) during the critical development stage of wheat and grain yield. Wheat was sown at two sowing dates: normal sowing window (Sowing 1) and late (Sowing 2) in Leeton and Wagga Wagga.

Figure 8

Figure 4. Regression analysis of mean maximum temperature and grain number per square metre during the critical development stage. Wheat was sown at two sowing dates: (normal sowing window (Sowing 1) and late (Sowing 2) in Leeton and Wagga Wagga.

Figure 9

Figure 5. Regression analysis of the photothermal quotient (PQ) during the critical development stage of wheat and grain yield. Wheat was sown at two sowing dates: (normal sowing window (Sowing 1) and late (Sowing 2) in Leeton and Wagga Wagga.

Figure 10

Figure 6. Regression analysis of the photothermal quotient corrected by vapour pressure deficit (PQvpd) during the critical development stage of wheat and grain yield. Wheat was sown at two sowing dates: (normal sowing window (Sowing 1) and late (Sowing 2) in Leeton and Wagga Wagga.

Figure 11

Figure 7. Regression analysis of the maximum temperature during the critical development stage of wheat and grain protein. Wheat was sown at two sowing dates: (normal sowing window (Sowing 1) and late (Sowing 2) in Leeton and Wagga Wagga.