Next Article in Journal
Low-Temperature-Induced Winter Dormancy in a Predatory Stink Bug Eocanthecona furcellata (Wolff) in the Subtropics
Previous Article in Journal
Inoculum of a Native Microbial Starter Cocktail to Optimize Fine-Aroma Cocoa (Theobroma cacao) Bean Fermentation
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Characteristic Identification of Heat Exposure Based on Disaster Events for Single-Season Rice along the Middle and Lower Reaches of the Yangtze River, China

1
Collaborative Innovation Center on Forecast and Evaluation of Meteorological Disasters, Nanjing University of Information Science & Technology, Nanjing 210044, China
2
State Key Laboratory of Severe Weather, Chinese Academy of Meteorological Sciences, Beijing 100081, China
3
National Meteorological Center, Beijing 100081, China
4
Department of Atmospheric Science, School of Environmental Studies, China University of Geosciences, Wuhan 430074, China
*
Author to whom correspondence should be addressed.
Agronomy 2023, 13(10), 2574; https://doi.org/10.3390/agronomy13102574
Submission received: 14 September 2023 / Revised: 27 September 2023 / Accepted: 1 October 2023 / Published: 7 October 2023
(This article belongs to the Section Precision and Digital Agriculture)

Abstract

:
As global warming continues, heat stress events are expected to increase and negatively affect rice production. Spatiotemporal changes in single-season rice exposure to heat stress were explored along the middle and lower reaches of the Yangtze River (MLRYR) in China during 1971–2020 based on created heat thresholds in different phenological stages, derived from comparison of historical heat records for single-season rice and agro-meteorological data. The feature importance (IF) provided by the Random Forest model was used to modulate the relationship between threshold accumulated temperature and yield reduction rate caused by heat stress. In addition, critical temperature thresholds at different phenological stages were determined by combining Overall Accuracy and the Receiver Operating Characteristic (ROC) curve. According to historical disaster records, the heat stress occurred before the reproductive phase (i.e., the tillering–jointing stage) and ended in the filling stage. Critical temperature thresholds of Tmax at tillering–jointing, booting, flowering and filling were quantified as 36, 35, 35 and 38 °C, with higher IF values of 13.14, 10.93, 17.15 and 13.15, respectively. The respective values of Overall Accuracy and the areas under the ROC curve were greater than 0.85 and 0.930, implying that each threshold performed excellently in identifying heat occurrence. Based on the determined critical thresholds, accumulated harmful temperature (Tcum), number of heat days (HD), first heat date (FHD) and last heat date (LHD) were presented to characterize heat exposure. It was clear that Tcum and HD exhibited a north-to-south increasing trend from 1971 to 2020, with the obvious increasing occurrence in most parts of the study region through the period of 2010 to 2020. FHD occurred earlier in most stations except the northeast parts, while LHD ended later in southern MLRYR. Exploring heat critical thresholds at different phenological stages highlighted in this study can help decision-makers monitor and evaluate heat exposure to single-season rice in MLRYR and further develop mitigation strategies to ensure rice production security.

1. Introduction

Rice (Oryza sativa L.) is a crucial cereal grain worldwide, serving as a primary source of sustenance for over 50% of the world’s population. Around 160 million hectares of agricultural land are dedicated to rice cultivation worldwide [1]. Experts estimate that the production of rice and other crops must increase by over 70% to meet the dietary demands of the world’s rapidly growing population by the year 2050. This increase in production is necessary to prevent food shortages and crises [2,3,4]. However, rice grown in the tropics and subtropics may be potentially at a greater risk of heat stress. Heat stress is recognized as an essential threat to rice cultivation in China [5], Sudan, Laos, India [6,7], etc., with increased frequency and severity in extreme temperature events induced by global warming across the major rice planting areas [8,9]. In China, there have been numerous instances of extreme heat events for rice from June to August after the annual plum rain season, specifically around the middle and lower reaches of the Yangtze River (MLRYR). The severe economic loss and grain reduction caused by heat disasters have occurred multiple times in MLRYR. For instance, heat events in 2003 contributed to a 5.18 million tons reduction in the predicted grain harvest and more than USD 1.5 billion in economic loss [10,11]. Following global warming, the frequency and intensity of extreme heat events have substantially increased in major parts of the world [12], posing challenges to rice production [13]. In MLRYR, the occurrence of rice heat stress has fluctuated markedly from year to year, with an overall increasing trend in the occurrence frequency and intensity [14]. Hence, it is essential to understand how rice responds to heat exposure in MLRYR, which can guide the implementation of targeted measures to reduce economic and production losses.
Heat stress is generally acknowledged as irreversible damage to spikelet fertility and yields during the growing season when elevated temperatures are beyond the expected threshold [15], as a consequence of spikelet sterility, reduced kernel weights, and a shorter grain-filling stage [16,17,18]. Under the constant temperature of 38 to 40 °C, the number of unfertilized grains is significantly increased and eventually depressed total grain yield [4,19,20]. Based on high-temperature controlling experiments, empirical statistical approaches or crop simulation models, several studies [21,22,23,24] have explored rice’s response to heat stress during the reproductive phases, e.g., the booting, flowering and filling stages [25]. Sanchez et al. [26] reviewed previous studies and concluded that rice yield was most sensitive to high temperature before flowering throughout the whole reproductive phase, followed by the grain-filling stage, which was contradictory with the result derived from the WOFOST crop model [27]. The current research on the effects of rice heat stress has generated some controversy regarding the varying sensitivities of rice growth stages. This lack of a precise explanation makes it challenging to assess the degrees of damage caused by unique heat events on rice during different growth stages. Such an assessment is significant in evaluating the intensity of rice heat stress exposure.
To accurately gauge the intensity of heat stress on rice, two basic aspects must be considered. First is the heat stress event, including the intensity, duration, and degree of elevated temperature [28]. Second is the rice’s resistance to heat stress, which varies depending on its growth stage [25]. It is widely accepted that the heat stress process is defined according to the threshold of average temperature (Tave) at 30 °C or maximum temperature (Tmax) at 35 °C for more than 3 consecutive days throughout the reproductive phase [5,9,14,24,25]. To some extent, it is difficult to accurately evaluate the state of each unique heat process, neglecting the difference in the disaster-causing degree. Although these studies can better explain the yield variation corresponding to the increase in temperature, the intensity of heat stress is often exaggerated or underestimated due to the lack of consideration of differences in the heat tolerance of rice at different growth stages. Rapid climate warming causes earlier heat stress occurrences, such as identifying heat stress at the vegetative phase (e.g., the seeding, tillering, and jointing stage), which was generally not cited previously [5,22,25,26]. Subjected to heat stress in the vegetative phase, rice is likely to be exposed to scorching senescence of leaves followed by abscission, and reduced plant height, tiller number, and biomass [4,28], especially tiller number per plant determines panicle number [17]. To effectively manage heat stress on rice crops, it is essential to integrate the identification of specific phenological stages with severe heat hits. The same temperature threshold was generally utilized only to reflect a certain degree of impact on rice growth but not necessarily involve different impacts in different phenological stages. Therefore, the altered heat resistance of rice should be identified during the dynamic growth.
Agro-disaster representations integrating disaster records and meteorological and crop phenology data [25] can be explored to reveal the relationship between meteorological factors and crop yields due to the disaster process and to redefine optimal triggering thresholds at different physiological stages. Moreover, whether rice exposure to heat stress only occurs at the reproductive phase and subsequent results from sensitivity to heat stress are still controversial and need to be deeply explored. In this paper, we used historical rice heat-disaster representations in MLRYR to determine the triggering threshold of heat stress occurrence and characterize single-season rice exposure to heat stress. The main objectives are: (1) to investigate the key phenological stages of rice exposure to heat stress based on the historical disaster data; (2) to quantify the critical temperature threshold for heat stress to single-season rice at different phenological stages; and (3) to delineate the characteristics of heat exposure, which can help us to develop strategies for adaptation to heat stress in MLRYR.

2. Material and Methods

2.1. Study Region

The study region spans across Jiangsu (JS), Zhejiang (ZJ), Anhui (AH), Jiangxi (JX), Hubei (HB) and Hunan (HN) Province, situated in MLRYR ranging between 24–35° N latitude and 109–123° E longitude (Figure 1). Under the control of a subtropical monsoon climate, the MLRYR is characterized by hot and rainy summers and cold and dry winters. Annual mean temperature ranges from 14 to 20 °C. Average annual precipitation is approximately 1000–1400 mm, with 40–60% occurring from June to August. The dominant rice cropping systems are double-cropped and single-cropped systems, including three types of rice (double-season early, double-season late and single-season rice). With the adjustment of planting structure and the shortage of workforce, the planting area of single-season rice in MLRYR has significantly increased in the past decades [29], accounting for approximately 73% of the rice cultivated area by 2020 [30]. The transplant stage of single-season rice in this region is typically in May and harvest in mid-to-late September. The phenological stages of single-season rice are consistent with the temporal distribution of hot weather in MLRYR, and overwhelming heat stress events occur in the reproductive phase, as has been demonstrated previously [20,31,32].

2.2. Data Description

Datasets including meteorological, phenology, yield, and disaster data were used to construct heat-disaster samples (Table 1). Meteorological data at 501 meteorological stations, including daily maximum temperature (Tmax) from 1971 to 2020, were used to explore the critical temperature threshold for characterizing the occurrence of heat stress to single-season rice, downloaded from the National Meteorological Information Center, China Meteorological Administration (Figure 1). Several missing values of meteorological data were replaced by the average value in the adjacent two days. Phenology data include average seeding, tillering, jointing, booting, flowering, and filling dates of single-season rice during 1981–2010, and were obtained from 34 agro-meteorological experimental stations of six provinces. The Kriging method was applied to interpolate phenology data to 501 stations. Single-season rice begins to flower in the last ten days of July in eastern MLRYR, while rice beginning to flower is delayed until early August in the western areas. The yield data of single-season rice at the provincial level has been archived by the National Bureau of Statistics (https://data.stats.gov.cn, accessed on 21 August 2022 ) from 1971 to 2020. The yield reduction rates (YRRs) were calculated by separating the trend yield fitted to adopting the method of the linear moving average. Historical heat events of single-season rice, including the time, location, and disaster degree, can be recorded in the Yearbook of Meteorological Disasters in China [33] and the China Meteorological Disasters Book (JS, ZJ, AH, JX, HB and HN) [34]. The aforementioned data were used to construct heat-disaster samples, facilitating the construction of the optimal caused-disaster thresholds for different growth phases. Meteorological data and phenology data were used for calculating accumulated harmful temperature (Tcum), number of heat days (HD), first heat date (FHD) and last heat date (LHD) to evaluate single-season rice heat stress exposure in MLRYR.

2.3. The Construction of Rice Heat Stress-Disaster Samples

Documentary evidence of historical agro-disaster events can provide disaster information for relevant studies [25,35,36]. Destruction evidence and methodology data can be coupled to explore the disaster weather conditions that can trigger crop damage [25,37]. The critical values of catastrophe characteristics can be obtained by comparing the difference in weather conditions between the disaster process and a historical non-disaster process. Using historical data on rice heat stress events and meteorological conditions, the exact phenological stages and thermal conditions were screened out to trigger heat occurrence in single-season rice in MLRYR. Then, Tmax was extracted to construct heat (H) and non-heat (NH) databases according to the historical disaster representations and exact phenological stages, integrating growth stage, location, occurrence time, and final time to identify optimally the critical threshold of heat stress for single-season rice.

2.3.1. Target Phenological Stages of Rice Heat Stress

Due to the unique combination of crop phenology and local climate, the thermal-sensitive period to heat stress likely differed between regions [9,38]. The national standard of the People’s Republic of China [39] stipulated that booting, flowering, and filling were the crucial stages in the heat stress process for single-season rice, as extensively studied in the literature [5,24]. Out of our historical heat representations of single-season rice, the earliest heat record was set on June 11 in JS province (early tillering stage), while the last instance of rice heat stress at the latest was recorded on 9 September in ZJ province (late filling stage). Furthermore, regardless of the rice characteristics and climate warming trends, the investigated phenological stages focused on the tillering–jointing, booting, flowering and filling stages, broadly grouped into one vegetative and three reproductive stages.

2.3.2. Construction of Heat (H) and Non-Heat (NH) Databases

Variations in the shape of the temperature distribution played a more crucial role, with notable damage from extreme temperature rather than the mean values. For instance, even a few hours of peak high temperature during the critical flowering or reproductive phase could drastically cause physiological damage and lead to vital crop failure, independently of any substantial changes in the mean state [14,22,40]. Given extensive cognition and high sensitivity to extreme temperatures on rice plants, Tmax was better developed as a critical temperature threshold for triggering single-season rice heat stress rather than the mean temperature in this study.
According to historical heat records for single-season rice in MLRYR, disaster samples, including the Tmax, growth stage, location, occurrence time and final time for each heat process, were integrated into the preliminary databases separately. Since our research hypothesis for this paper was that there were different heat stress thresholds in each phenological stage, historical heat-disaster samples screened from the preliminary database that only heat stress affects a single growth stage were reintegrated into the new databases, denoted as the H database here. All Tmax values from each heat sample were considered thermal conditions for single-season rice to demonstrate the altered status during the temporal span of a heat process/event. To better identify rice heat stress, the NH database was constructed by a collection of Tmax values over the previous 5 days based on disaster records, which represented the temperature conditions that did not trigger rice heat stress. Additionally, we used clear heat-disaster records covering multiple phenological stages as application validation samples to verify the availability of critical temperature thresholds for single-season rice in MLRYR.
For instance, consider the following disaster record: “20 July–2 August 2016, ear differentiation and inflorescence emergence of single-season rice in Hefei (AH province) were affected by high-temperature weather, and rice was damaged with yield decreased”. Following the representation of meteorological data, the Tmax values of the corresponding meteorological station and temporal span at Hefei were 33, 34.3, 36, 37.4, 37.7, 38.2, 39.1, 38.5, 37.8, 38.2, 38.7, 37.7, 35.7, and 35 °C, also labeled as a flowering sample in H database. Meanwhile, the Tmax values 15–19 July (the prior 5 days) and 3–7 August (the previous 5 days) of 30.8, 29.7, 32.8, 33.5, 28.5 °C and 31.5, 32.5, 31.9, 33.6, 32.2 °C, respectively, were also retrieved and were labeled as two flowering samples of single-season rice in the NH database. Finally, the H database collated 122 tillering–jointing samples, 108 booting samples, 148 flowering samples, and 237 filling samples, as well as the NH database including 144 tillering–jointing samples, 216 booting samples, 296 flowering samples, and 474 filling samples.

2.4. Critical Threshold Identification for Rice Heat Stress

There were complex nonlinear relationships between crop growth and meteorological conditions that were not straightforward. While traditional Pearson correlation analysis typically determined the relationship between two variables, it fell short in measuring nonlinear relationships [41]. As a widely used machine learning decision tree model, Random Forest can handle the nonlinear relationship among the variables by utilizing a non-parametric algorithm. The IF is the importance score obtained from model training that can rank the relative importance of each predictor variable in controlling the response variable [41,42]. To determine different threshold temperatures that damage the yield under heat exposure, the Random Forest model was applied in this study to explore the first three key threshold temperatures highly correlated with YRR, which were preliminary screened out by the higher IF value. Then, the Overall Accuracy and Receiver Operating Characteristic (ROC) curves were often used to provide accuracy between the constructed H and NH databases in classification algorithms and were combined to identify optimum critical thresholds for different growth stages on the principle of high IF values and high accuracy.

2.4.1. The Importance Score of Random Forest (IF)

Random Forest was used to establish the model between accumulated temperature calculated by different threshold values and YRR of single-season rice. The IF is based on the out-of-bag (OOB) regression prediction error. The variable importance is computed by mean square error ( M S E O O B ):
M S E O O B = 1 n k = 1 n n D k D O O B , k 2
where n n is the number of observations, D O O B , k is the average of all OOB predictions across all trees in Random Forest. IF is estimated using the “%IncMSE” metric in the Random Forest model. This process was implemented using the package “random forest” in Python 3.9.

2.4.2. Overall Accuracy

Overall Accuracy is measured as how accurately Tmax can trigger rice heat stress and indicates the proportion of correct retrievals for both heat occurrences and non-occurrences.
O v e r a l l   A c c u r a c y = T P + T N T P + T N + F P + F N
Here, true positives ( T P ) are the number of rice heat stress instances in the H database that are retrieved correctly; false positives ( F P ) are the number of non-heat samples in the NH database that are retrieved incorrectly; true negatives ( T N ) are the number of non-heat samples in the NH database that are retrieved correctly and false negatives ( F N ) are the number of rice heat stress instances in the H database that are retrieved incorrectly.

2.4.3. ROC Curve

The ROC curve is a graphical representation used to display the diagnostic ability of binary classifiers and obtain a more comprehensive accuracy with variation in the diagnostic threshold, as well as the change in true and false positive fractions. It is widely used in various fields of study, including medicine, radiology, natural hazards, and machine learning [43]. The ROC curve is constructed by plotting multiple pairs of true positive rate ( T P R ) values against false positive rate ( F P R ) values. T P R represents the proportion of observations that are correctly (truly) retrieved to be positive out of all positive observations ( T P + F N ). Similarly, F P R is the proportion of observations that are incorrectly (falsely) retrieved to be positive out of all negative observations ( T N + F P ).
T P R s e n s i t i v i t y = T P T P + F N
F P R 1 s e n s i t i v i t y = F P T N + F P
With F P R as the x-coordinate and T P R as the y-coordinate, the ROC curve is drawn and shows the trade-off between sensitivity ( T P R ) and specificity ( 1 F P R ) by changing the diagnostic threshold. The ROC curve was used to evaluate how well the predictor (Tmax) could identify whether rice heat stress would occur or not. The AUC value, which represents the area under the ROC curve, provides an estimate of the overall performance of Tmax. The evaluation standard is AUC < 0.6 (Fail), 0.6 ≤ AUC < 0.7 (Poor), 0.7 ≤ AUC < 0.8 (Fair), 0.8 ≤ AUC < 0.9 (Good), 0.9 ≤ AUC ≤ 1 (Excellent).

2.5. Characteristics of Rice Heat Stress

2.5.1. Accumulated Harmful Temperature (Tcum) and Number of Heat Days (HD)

Tcum is the sum of temperature differences that exceed the critical threshold, while HD is the number of rice heat stress days at different phenology per station from 1971 to 2020. Tcum and HD can effectively assess the frequency and intensity of heat exposure to single-season rice under observed contemporary climate conditions in MLRYR. The Mann–Kendall (MK) test, a rank-based nonparametric method, detected statistically significant trends and mutation time of heat exposure in rice over a 50-year period. Its advantage is that a nonparametric test is not disturbed by outliers, and sample data does not need to follow a certain distribution. In this paper, the null hypothesis (H0) was that there has been no trend in heat exposure over time; the alternate hypothesis (H1) was that there has been a trend (increasing or decreasing) over time. The mathematical equations for calculating MK Statistics S ,   E S , v a r S   are as follows:
S = i = 1 n 1 j = i + 1 n s i g ( X j X i )
s i g X j X i = + 1   i f   X j X i > 0 0   i f   X j X i 0
Under the assumption of random independence of the time series, the standardized test statistic U F is defined as follows:
U F = S E S v a r S
E S = n n 1 4   v a r S = n n 1 2 n + 5 72
Then, repeat the   S and s i g X j X i   procedures with inverse time series to define the statistic U B :
U B = S E S v a r S
In these equations, X j and X i are the time series observations in chronological order, n is the length of the time series,   S   is the cumulative number of time i values greater than time j values, and E S and v a r S are, respectively, the mean and variance of   S . Positive U F values indicate an upward trend in the time series; negative U B values indicate a negative trend. If U F > U F 1 α / 2 , (H0) is rejected, and a statistically significant trend exists in the time series of heat exposure. The critical value of U F 1 α / 2 for a significance value of 0.05 from the standard normal table is 1.96. Similarly, if U B >1.96, there is a statistically significant trend in the inverse time series. The intersection of U F and U B curves occurs in the range [−1.96, 1.96], then the intersection is when the mutation starts, the mutation point.

2.5.2. First Heat Date (FHD) and Last Heat Date (LHD)

The formation of rice heat stress is a dynamic process of gradual accumulation [44], from the temperature increasing gradually to the critical threshold of normal crop growth and the continuous high temperature until rice is damaged to varying degrees. Generally speaking, most domestic studies consider a heat process where the maximum air temperature exceeds the critical threshold for at least 3 days. So, the date when the first heat process occurred was regarded as FHD. Similarly, the end date of the last heat process was considered to be LHD.

3. Result

3.1. Characteristics of the Heat (H) and Non-Heat (NH) Databases

Clear differences in Tmax values showed significantly higher Tmax values in the H database than in the NH database at similar phenological stages (Table 2). Take the mean value as an example; the difference between H and NH databases at tillering–jointing, booting, flowering and filling stages were 3.39, 4.69, 5.75 and 3.67 °C, respectively. The mean values of Tmax in the H database showed an increasing trend with the advancement of the growth period and were 33.69, 36.31, 36.43 and 36.82 °C, respectively. The violin plots in Figure 2 showed the detailed distribution of Tmax values in H and NH databases for single-season rice. It could be seen that most values in the H database were distributed ranging from 30 °C to 40 °C, accounting for nearly 90% of all Tmax values. From the H databases of different phenological stages, Tmax from 36 to 37 °C was detected as having the highest frequency of single-season rice heat stress in the tillering–jointing database, accounting for 13.23% of Tmax values detected in this range. The highest frequencies at booting, flowering and filling were located in the range 35~36 °C, 37~38 °C and 37~38 °C, with 20.40%, 19.78%, and 20.81% of Tmax values in the H database, respectively. From the perspective of the NH−5 and NH+5 databases, the distributed core range of sample values in NH−5 databases was higher than that of NH+5 databases. The study determined the critical threshold temperature for triggering heat occurrence to single-season rice as 30~40 °C.

3.2. Critical Threshold Identification for Heat Occurrence to Single-Season Rice

3.2.1. The First Three Key Thresholds Explored Preliminary

The important results of 11 different test thresholds from 30 to 40 °C with 1 step are present in Figure 3. It can be seen that the IF values at different phenological stages had a certain degree of volatility, showing a trend of initially decreasing, then increasing, and then decreasing with the increase of test thresholds. The first three IF values at tillering–jointing are 30, 32, and 36 °C, with scores of 17.8, 14.02, and 13.14, respectively. The top three IF values at booting and flowering were homogeneously 30, 31, and 35 °C. The test threshold of 35 °C at flowering had the highest importance score with a value of 17.15, while 30 °C at booting ranked first with a score of 18.82, followed by 31 and 35 °C at booting, with scores of 12.47 and 10.93. Relatively speaking, test thresholds at filling ranked first three IF values were higher than those in other phenological stages, with the first three higher scores being 11.62 at 31 °C, 12.95 at 37 °C, and 13.15 at 38 °C.

3.2.2. Optimal Critical Threshold for Heat Occurrence at Each Phenological Stage

Overall Accuracy values from 30 to 40 °C with 1 step for heat occurrence were calculated and demonstrated in Figure 4, while the detailed statistics for TP, TN, FP, FN, Overall Accuracy, TPR, and FPR corresponding to the first three key thresholds were listed in Table 3. Lower thresholds like 30–32°C correctly identified heat samples (with all TPR values of 1) but falsely identified non-heat samples (with FPR values from 0.776 to 0.988), resulting in lower Overall Accuracy (without the values above 0.5). For tillering–jointing, the peak of Overall Accuracy was set at the test threshold of 36 °C (exactly 0.975) with higher TPR and lower FPR. As for booting and flowering, despite being below the maximum value, 35 °C still had a high level of Overall Accuracy (exactly 0.861 and 0.903) with a high rate of correctly recognizing heat occurrence (TPR = 1) and a low rate of falsely recognizing non-heat occurrence (FPR, 0.208 at booting and 0.145 at flowering). Given that the optimal critical threshold must concurrently have a high IF value, high Overall Accuracy, high TPR and low FPR, test thresholds of 36 °C at booting and 37 °C at flowering were discarded due to low IF values below 10. The optimal critical threshold at filling was 38 °C, which had the highest Overall Accuracy and IF values.
The ROC curves for each phenological stage were drawn in Figure 5, illustrating a trade-off between achieving a high true-positive rate and a low false-positive rate. Each test point on the ROC plot referred to a sensitivity-specificity pair corresponding to a particular decision threshold. AUC values were obtained from TPRs and FPRs at each test point, reaching 0.993 at tillering–jointing, 0.959 at booting, 0.989 at flowering, and 0.930 at filling, corresponding to ‘excellent’ performances of Tmax as the trigger factor to discriminate whether heat occurred or no heat. Measured comprehensively by the method above, the Tmax values of 36, 35, 35. and 38 °C were sequentially confirmed as the optimal critical threshold for identifying the occurrence of heat exposure to single-season rice in MLRYR as the phenological stage advanced.

3.2.3. Verification and Application of a Multi-Stage Heat Event

The effects of long-time series of high-temperature events on crops are more complex and severe. According to the heat-disaster record, the southeast HB province suffered from the heat weather process for the first time during 2~6 July 2013 (day of the year (DOY) 183~187, tillering–jointing). Later, the single-season rice in this region was heavily affected by heat stress from 21 to 30 July (DOY 202~211, late booting and early flowering). After that, the grain filling of single-season rice was damaged again by the third heatwave process during the period from 13 to 18 August (DOY 225~230, filling). Tmax values were analyzed from 21 stations in southeast HB from 2 July to 18 August (DOY 183~230), including a three-stage actual heat process indicated by the grey-shaded area (Figure 6). Similar to the previously described construction of heat and non-heat samples, the Tmax values of 21 locations corresponding to 27 June~1 July and 19~23 August (DOY 178~182 and DOY 231~235, respectively) were checked as the previous 5 days of non-heat process (Figure 6). Temperature values for the verification process of this whole heat event fluctuated significantly, and the daily Tmax values reached the peaks in three grey shadow areas, respectively.
During the first heat process (DOY 183~187), 28.5% of stations with Tmax values above 36 °C showed heat stress one day ahead of the actual heatwave occurred. The air temperature was continuously heated until the Tmax of all stations was greater than 36 °C after 2 days (DOY 184). The heat gradually decreased but remained high until all stations were judged to be non-heat on DOY 188, consistent with the actual record ending of the first heat wave. In terms of the second heatwave on record (DOY 202~211), only 1~2 stations from DOY 197 to 201 exceeded the determined threshold of 35 °C, with a difference of about 0.2 to 0.6 °C. Rice heat stress occurred on DOY 202, with 12 locations identifying heat development, and air temperatures continued to rise through DOY 203 to 205. On DOY 206, all stations experienced heat stress with up to 1.8~5.1 °C difference from the threshold. Severe high temperatures persisted until DOY 211, with the proportion of heat stations decreasing to 71.4%. The southeast HB was judged to be the first day that non-heat occurred on DOY 215, a delay of 3 days compared to the actual heat record. The third heat process occurred during DOY 225~230, and heatwave start-up determined by the 38 °C threshold was delayed by one day with five stations on DOY 226. 94.5% of the stations were identified as heat stations on DOY 228, reaching the peak ratio during this third process. The third heatwave ended on DOY 230, exactly consistent with disaster records in MLRYR, as only one station had Tmax above 38 °C on DOY 231. It was evident that various temperature thresholds were robust and reliable indicators in identifying heat stress on single-season rice at different phenological stages.

3.3. Characteristics of Heat Exposure for Single-Season Rice in MLRYR

3.3.1. Accumulated Harmful Temperature (Tcum) and Number of Heat Days (HD)

The spatiotemporal distribution characteristics were explored from 1971 to 2020. From a spatial perspective (Figure 7a–d), the regional mean of Tcum from tillering–jointing to filling followed a response of first increasing and then decreasing, and the corresponding mean Tcum reached its maximum value of 8.7 °C at flowering. High Tcums were mainly found in mid-western ZJ, mid-eastern JX, and a small part of areas in HN at booting, as well as the southern region of MLRYR at flowering (e.g., mid-eastern HN, central JX, western ZJ and the southeast corner of HB), with Tcum values for 19.7% stations at booting and 30.1% stations at flowering greater than 12 °C. The Tcums at tillering–jointing and filling were comparatively lower, with the observed Tcum for most stations being less than 6 °C. According to the spatial distribution of HD (Figure 7e–h), the average annual HD of most locations at tillering–jointing and filling were below 4 d, while there were generally greater than 4 days of high-temperature weather at booting in southern MLRYR. The region with high HD values above 6 d at booting was the same as the high Tcum-dominated region, accounting for 32.5% of heat stations. Compared to the HD at flowering, the range of heat stress with HD values above 4 d for single-season rice was wider than that at booting, and HD gradually decreased from south to north in this region. In addition, the number of non-heat stations reached 64 for single-season rice at filling, accounting for nearly 12.8% of the 501 meteorological stations in MLRYR, followed by tillering–jointing with 16 locations. Overall, the middle and northeast parts of the study region were considered regions with a high frequency of rice heat stress.
In the past 50 years (Figure 8), high occurrence times of rice heat stress were mainly concentrated in 1971, 1978, 1988, 2003, 2007, 2013 and 2017, with the regional HD for each station being greater than 16 d. Among them, Tcum in 2003, 2013 and 2017 assumed a leading position, with values of 49.9, 54.9 and 41.3 °C, respectively. The MK test showed that the temporal variation characteristics of HD were consistent with that of Tcum (Figure 9), with both showing a decreasing trend first since 1971 and then gradually increasing after 2000, which was also considered a mutation point. It is worth noting that Tcum and HD increased significantly since 2010 (p < 0.05). Therefore, the period was divided into three slices, i.e., 1971–2000, 2001–2009, and 2010–2020, to distill the difference in mean trends of Tcum and HD (Figure 10). It was clear that Tcum and HD were relatively low during 1971–2000 but increased during 2001–2009 and 2010–2020.

3.3.2. First Heat Date (FHD) and Last Heat Date (LHD)

It was obvious that FHD of 59.9% stations occurred earlier on DOY 162–168 (early tillering–jointing, Figure 11a), as heat stress for single-season rice occurred later in the northeast corner of MLRYR on DOY 179–188 (late tillering–jointing and early booting). On the contrary, the heat process ended later in the earlier FHD region with a high LHD of DOY 224–243 (filling, Figure 11b), and the northeast corner of MLRYR and central HB region showed the non-heat state earlier with the lower LHD of DOY 204–213 (flowering). Only four stations did not recognize the heat for single-season rice throughout the investigated phenological stages.

4. Discussion

4.1. Determined Thresholds for Different Phenological Stages

Over the past years, the advancement in crop simulation models, climatic models and machine learning have made it possible to explore the impacts of extreme climate events on crop growth and yield on a large scale, over a long sequence as well as from multi-dimensions [5,9,22,24]. Identification indicators for agro-meteorological disasters and the criteria to distinguish the occurrence of crop disasters are the basis for the research on hazard damage mechanisms, spatiotemporal distribution characteristics, monitoring and early warning, as well as risk assessment. In this paper, critical temperature thresholds (Tmax) for various phenological stages were established to reflect the ability to identify heat stress for single-season rice in MLRYR. Based on meteorological data combined with historical disaster records, regional thermal hazard indicators were constructed as 36 °C at tillering–jointing, 35 °C at booting–flowering and 38 °C at filling, respectively. As exhibited in a series of heat control experiments, exposure to 5d above 35 °C at flowering could result in up to 90% spikelet sterility [17,23]. In contrast, the negative impacts of high temperatures (over 35 °C) at tillering were considerably less, meaning that rice could tolerate relatively high temperatures at the vegetative phase [7,45,46]. High temperature (38 °C day/30 °C night) in the Aus type N22 for 6 h increased 29% spikelet sterility at flowering [47], while identical treatment for 20 consecutive days at filling reduced 24.6% grain weight [48]. Rice plants suffering from 40 °C for 10~15 d at tillering and filling showed about 86% and 13% lower total yield per plant, respectively [49,50]. The differences observed between temperature thresholds and the results mentioned above collectively indicate that rice’s tolerance and sensitivity to high temperatures vary depending on the growth stage, with the booting and flowering stages being the most sensitive stages, followed by tillering–jointing and filling. As confirmed in previous studies [4,25,51], hot weather before and during flowering tended to lead to more severe heat stress for rice. Heat stress occurring during the vegetative phase could affect tiller formation, and its extended heat exposure during the booting stage would impact spikelet meristem differentiation [52]. The influence of hot weather on rice filling is controversial. It was reported that a certain degree of heat stress could compensate for reduced grain-filling duration by increased filling rates [23,48,53], while some researchers believed it affected the photosynthesis and material migration of rice, thereby altering grain size, increasing grain chalkiness and then reducing grain quality and weight [4,46,53,54,55].
The critical temperature threshold for rice heat stress varies due to the complexity of disaster occurrence, the roles of agronomic management practices, and crop genetic backgrounds [4,14]. Given the adaptation of rice plants to local climate and environment, even the same variety of rice in different regions may have different thresholds, and it implies that heat critical threshold could be of regional practicality and variety limitations. For instance, experts have reported that high day temperature (38 °C) during anthesis can reduce the number of pollen grains on the stigma in the Aus type N22 by 55% and the japonica type Moroberekan by 86%, but not in the indica type IR64 [47]. This difference in susceptibility to heat stress is attributed to different genetic backgrounds. In this research, the importance analysis, overall accuracy and ROC curve were jointly used to gain the optimal threshold for single-season rice in MLRYR, comprehensively considering the proportions of correctly identified heat (TPR) events and incorrectly identified non-heat (FPR) events. The model for identifying heat or non-heat occurrence to single-season rice based on daily Tmax performed excellently at each phenological stage, with relative IF values and AUC values greater than 10 and 0.930, respectively. This kind of historical disaster-based indicators construction method has been widely used in coping with disaster indexes for agro-meteorological disasters, such as heat [25], drought [37,56] and frost [57,58], avoiding the effects of subjective factors and the limitations of experimental regions.
Furthermore, a multi-stage heat event with long time series was checked for conformity to the disaster record based on the confirmed critical thresholds at different phenological stages (Figure 6), and the results indicated that the single-season heat indicators can reasonably reflect actual heat exposure in regional scales. As rice heat stress exposure in MLRYR was always highlighted and more severe than in other regions, the typical variety in MLRYR was considered in the study. However, it was definite that the characteristics of heat exposure might be different as regional conditions and rice varieties might vary. Although refined thresholds for different growth stages might not play the best application in some specific regions, these thresholds could be of practicality in regions with the same latitude and with similar rice varieties. Of course, the application of the proposed method should be further explored in other climatic regions and varieties.

4.2. Potential Adaption Strategies to Mitigate Rice Heat Stress

It is an indisputable fact that global warming has a negative impact on rice yield by accelerating the growth process of rice and shortening its biomass accumulation time [41,59]. The relationship between rice yields and temperature varied with the extent of rising temperature and region baseline temperature [60]. The higher baseline temperature leads to greater heat stress for rice under future global warming.
Decision-makers should highlight the need to develop adaptive rice security mechanisms to mitigate the negative effects of warmer conditions. In our present work, extreme rice heat stress exposure in the southern MLRYR was more severe than that in the northern part (Figure 7), characterized by strong intensity and prolonged duration. The indica-type rice should be chosen as the main cultivation in the southern region instead of the Aus type and the japonica type. As concluded by previous reporters [47,61], the indica type was more tolerant to heat exposure than the remaining two. Derived from Figure 7 and Figure 11, rice plants at booting and flowering were greatly susceptible to extremely high temperatures, as well as having become increasingly fierce over the past decade (2010–2020, Figure 9 and Figure 10). Hence, appropriate adjusting of the rice’s sowing and transplanting dates [62], giving rise to variation in phenology length, can be an effective strategy to escape or avoid in the time of a crucial phenological phase subjected to heat exposure in the study region. Assuming that rice plants inevitably encounter high temperatures, several agronomic management practices can be taken into account by artificial control, e.g., altered flowering pattern, proper application of growth regulators such as CTK, SA, BR, and ethylene precursors or increased transpiration cooling of the canopy [4,7]. Obviously, most of the current adaption strategies are targeted at exposure to heat stress that occurred at the reproductive phase, but we advanced explored phase affected by heat stress to the tillering–jointing stage in MLRYR. In theory, the tiller number and panicle number have shown a strong and positive correlation in rice in both favorable or stress conditions [45]. Heat stress for the entire region, FHD of most sites occurred at early tillering (Figure 11a, high temperature during tiller formation should be paid equal attention, and some measures should be used to alleviate initial rice heat stress. Commonly, the tiller number is determined by a hormonal network of abscisic acid (ABA) and strigolactones [63,64]. Recent research [65] demonstrated that ABA could repress the outgrowth of unproductive tillers by regulating the non-participation of strigolactones in the formation of high-order tillers. Applying exogenous ABA or drying the field can promote the endogenous level of ABA so as to enhance the stress resistance of rice vegetative phase to heat stress, which has been presented in different abiotic stress tolerances, such as drought, high salinity, and cold [65,66,67].

4.3. Uncertainties and Limitations

According to extensive research and practice [5,9,14,24], 35 degrees Celsius has been identified as a critical temperature threshold for different development stages of rice plants. This study emphasized that heat thresholds were strongly influenced by local climate conditions, crop genetics, and evolving phenological stages, ultimately redefining the critical threshold library for single-season rice heat stress exposure in MLRYR. There were two relatively higher thresholds (36 °C and 38 °C) in this library established by the historical disaster-based indicators construction method. Compared to the threshold of 35 °C, higher thresholds might raise the risk of lack of ability to capture slight heat stress and lead to an underestimation of rice heat stress risk assessment. Even then, research results from MK test analysis of heat exposure via the investigated phenological phase still suggested that rice plants were increasingly being exposed to extreme heat with rising global mean temperatures since the 2000s, particularly with obvious increased trends in regional exposure since 2010. Moreover, such a trend would be more severe with future warming, which was consistent with the findings of previous studies [9,14,68]. In the near future, we could conduct field experiments under relevant critical temperatures at different phenological stages to verify the reliability of a critical threshold database or improve the precision of the threshold to decimal places at the region scale.
The phenology of single-season rice has varied over the years due to the influences of climate change and production demands. Consequently, a fixed threshold sowing date might not be appropriate for prediction in ongoing years, but we still lack proper ways to predict it currently. Meanwhile, warming temperatures increase the speed of crop development, which could potentially shift the timing of the reproductive phase in future climates [22]. Rough estimates are that 1 °C warming reduces the time to flowering by ~4 days [69], but this will vary by crop, variety and baseline temperatures. Apart from exposure to extreme reproductive heat, further factors could help to determine the overall crop response to environmental change (e.g., increasing atmospheric CO2 and O3 concentrations, changes in soil moisture and vapor pressure deficit, increases in mean temperatures, and the interactions between these changes). According to experts, elevated night temperatures have a determinant impact on yield and grain quality [52], and this trend seems to be accelerating more rapidly than day temperature. An important caveat concerns our inability to account for CO2 concentrations. Plants use CO2 as an input in the photosynthesis process; therefore, increasing CO2 levels may spur plant growth and yields. Yield declines stemming from extreme heat stress may be offset by CO2 fertilization [24,70]. Field experiments found that high temperature (35~38 °C) and high CO2 level (660 µmolmol−1) only had a positive impact on rice biomass but a negative impact on rice yields by reduced utilization of additional non-structural carbohydrates in the sink under heat exposure [70,71,72]. Rice plants grown under elevated CO2 would be more sensitive to heat stress [70,71]. To date, the magnitude of interaction on rice from both elevated temperature and increased CO2 is still debated and requires further investigation. Given the basis of previous studies, a comprehensive index for regional heat evaluation should be explored and constructed in future studies in order to jointly reflect the influence of the interaction between high temperature and its meteorological factors on rice plants and yield formation. The findings in our study can better assist the construction of a comprehensive index as fundamental information for the index exploration process.

5. Conclusions

Based on historical disaster records and daily maximum temperature (Tmax), a critical threshold database of rice heat stress at different growth stages was constructed to evaluate single-season rice heat stress exposure along MLRYR between 1971–2020. Tmax of 36 °C at tillering–jointing, 35 °C at booting, 35 °C at flowering and 38 °C at grain filling were identified as the critical thresholds for heat occurrence to single-season at different phenological stages, with relatively IF values and AUC values greater than 10, 0.930, respectively. A multi-stage heat event checked for conformity also showed that the critical threshold at each phenological stage could be applied to accurately identify heat events for rice plants in MLRYR. The spatiotemporal characteristics of heat stress for single-season rice in MLRYR were analyzed, and it was found that Tcum and HD increased from north to south, with most parts of the study region experiencing significant increases from 2010 to 2020 by the MK test. FHD occurred earlier for single-season rice across the region, except in the northeast corner, where it was later. Conversely, the LHD occurred later in the same area where FHD appeared earlier. Given the potential for future climate extremes, research on the critical temperature thresholds for heat stress to rice is of great significance for improving the rice heat stress meteorological service and for reducing yield and economic losses caused by heat stress.

Author Contributions

Conceptualization, M.J. and Z.H.; methodology, M.J., Z.H. and M.L.; validation: M.J., Z.H. and R.K.; formal analysis, M.J. and Q.M.; writing-original draft preparation, M.J. and Z.H.; writing—review and editing, M.J., Z.H. and L.Z. funding acquisition, Z.H. All authors have read and agreed to the published version of the manuscript.

Funding

This study is supported by the Science and Technology Development Foundation of the Chinese Academy of Meteorological Sciences (2023KJ024).

Data Availability Statement

Data available on request.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Sassaki, G.; Schmidt, A.B.; Ferreira, M.E.; Rangel, P.H.N.; Pereira-Netto, A.B. Characterization of cold-induced changes in the fatty acids profile of rice seedlings. Acta Physiol. Plant. 2013, 35, 1989–1996. [Google Scholar] [CrossRef]
  2. Farooq, M.S.; Khaskheli, M.A.; Uzair, M.; Xu, Y.; Wattoo, F.M.; Rehman, O.U.; Amatus, G.; Fatima, H.; Khan, S.A.; Fiaz, S.; et al. Inquiring the inter-relationships amongst grain-filling, grain-yield, and grain-quality of Japonica rice at high latitudes of China. Front. Genet. 2022, 13, 988256. [Google Scholar] [CrossRef] [PubMed]
  3. Farooq, M.S.; Uzair, M.; Raza, A.; Habib, M.; Xu, Y.; Yousuf, M.; Yang, S.H.; Ramzan Khan, M. Uncovering the research gaps to alleviate the negative impacts of climate change on food security: A review. Front. Plant Sci. 2022, 13, 927535. [Google Scholar] [CrossRef] [PubMed]
  4. Xu, Y.; Chu, C.; Yao, S. The impact of high-temperature stress on rice: Challenges and solutions. Crop J. 2021, 9, 963–976. [Google Scholar] [CrossRef]
  5. Zhang, L.; Yang, B.; Li, S.; Hou, Y.; Huang, D. Potential rice exposure to heat stress along the Yangtze River in China under RCP8.5 scenario. Agric. For. Meteorol. 2018, 248, 185–196. [Google Scholar] [CrossRef]
  6. Ishimaru, T.; Seefong, X.; Nallathambid, J.; Rajendrand, S. Quantifying rice spikelet sterility in potential heat-vulnerable regions Field surveys in Laos and southern India. Field Crops Res. 2016, 190, 3–9. [Google Scholar] [CrossRef]
  7. Wassmann, R.; Jagadish, S.V.K.; Sumfleth, K.; Pathak, H.; Howell, G.; Ismail, A.; Serraj, R.; Redona, E.; Singh, R.K.; Heuer, S. Regional vulnerability of climate change impacts on Asian rice production and scope for adaptation. Adv. Agron. 2009, 102, 59–122. [Google Scholar]
  8. Eyshi Rezaei, E.; Webber, H.; Gaiser, T.; Naab, J.; Ewert, F. Heat stress in cereals: Mechanisms and modelling. Eur. J. Agron. 2015, 64, 98–113. [Google Scholar] [CrossRef]
  9. Teixeira, E.I.; Fischer, G.; Van Velthuizen, H.; Walter, C.; Ewert, F. Global hot-spots of heat stress on agricultural crops due to climate change. Agric. For. Meteorol. 2013, 170, 206–215. [Google Scholar] [CrossRef]
  10. Tian, X.H.; Luo, H.W.; Zhou, H.D.; Wu, C.Y. Research on heat stress of rice in China: Progress and prospect. Chin. Agric. Sci. Bull. 2009, 25, 166–168. [Google Scholar]
  11. Laborte, A.; Nelson, A.; Jagadish, K.; Aunario, J.; Sparks, A.; Ye, C.; Redoña, E. Rice feels the heat. Rice Today 2012, 11, 30–31. [Google Scholar]
  12. Lee, O.; Seo, J.; Won, J.; Choi, J.; Kim, S. Future extreme heat wave events using Bayesian heat wave intensity-persistence day-frequency model and their uncertainty. Atmos. Res. 2021, 255, 105541. [Google Scholar] [CrossRef]
  13. Peng, S.; Tang, Q.; Zou, Y. Current status and challenges of rice production in China. Plant Prod. Sci. 2009, 12, 3–8. [Google Scholar] [CrossRef]
  14. Tao, F.; Zhang, S.; Zhang, Z. Changes in rice disasters across China in recent decades and the meteorological and agronomic causes. Reg. Environ. Change 2012, 13, 743–759. [Google Scholar] [CrossRef]
  15. Schlenker, W.; Roberts, M.J. Reply to Meerburg et al. Growing areas in Brazil and the United States with similar exposure to extreme heat have similar yields. Proc. Natl. Acad. Sci. 2009, 106, 121. [Google Scholar] [CrossRef]
  16. Reynolds, M.P.; Quilligan, E.; Aggarwal, P.K.; Bansal, K.C.; Cavalieri, A.J.; Chapman, S.C.; Chapotin, S.M.; Datta, S.K.; Duveiller, E.; Gill, K.S.; et al. An integrated approach to maintaining cereal productivity under climate change. Glob. Food Secur. 2016, 8, 9–18. [Google Scholar] [CrossRef]
  17. Krishnan, P.; Ramakrishnan, B.; Reddy, K.R.; Reddy, V.R. High-temperature effects on rice growth, yield, and grain quality. Adv. Agron. 2011, 111, 87–206. [Google Scholar]
  18. Lawas, L.M.F.; Shi, W.; Yoshimoto, M.; Hasegawa, T.; Hincha, D.K.; Zuther, E.; Jagadish, S.V.K. Combined drought and heat stress impact during flowering and grain filling in contrasting rice cultivars grown under field conditions. Field Crops Res. 2018, 229, 66–77. [Google Scholar] [CrossRef]
  19. Matsui, T.; Omasa, K.; Rorie, T. The difference in sterility due to high temperatures during the flowering period among Japonica rice varieties. Plant Prod. Sci. 2001, 4, 90–93. [Google Scholar] [CrossRef]
  20. Xie, X.J.; Li, B.B.; Li, Y.X.; Li, H.Y. Effects of high temperature stress on yield components and grain quality during heading stage. Chin. J. Agrometeorol. 2010, 31, 411–415. [Google Scholar]
  21. Shi, P.; Zhu, Y.; Tang, L.; Chen, J.; Sun, T.; Cao, W.; Tian, Y. Differential effects of temperature and duration of heat stress during anthesis and grain filling stages in rice. Environ. Exp. Bot. 2016, 132, 28–41. [Google Scholar] [CrossRef]
  22. Gourdji, S.M.; Sibley, A.M.; Lobell, D.B. Global crop exposure to critical high temperatures in the reproductive period: Historical trends and future projections. Environ. Res. Lett. 2013, 8, 024041. [Google Scholar] [CrossRef]
  23. Jagadish, S.V.; Craufurd, P.Q.; Wheeler, T.R. High temperature stress and spikelet fertility in rice (Oryza sativa L.). J. Exp. Bot. 2007, 58, 1627–1635. [Google Scholar] [CrossRef] [PubMed]
  24. Sun, Q.; Zhao, Y.; Zhang, Y.; Chen, S.; Ying, Q.; Lv, Z.; Che, X.; Wang, D. Heat stress may cause a significant reduction of rice yield in China under future climate scenarios. Sci. Total. Environ. 2022, 818, 151746. [Google Scholar] [CrossRef] [PubMed]
  25. Yang, J.; Huo, Z.; Li, X.; Wang, P.; Wu, D. Hot weather event-based characteristics of double-early rice heat risk: A study of Jiangxi province, South China. Ecol. Indic. 2020, 113, 106148. [Google Scholar] [CrossRef]
  26. Sanchez, B.; Rasmussen, A.; Porter, J.R. Temperatures and the growth and development of maize and rice: A review. Glob. Change Biol. 2014, 20, 408–417. [Google Scholar] [CrossRef]
  27. Wang, L.X.; Xu, X.L.; Li, Q.; Su, H. Impact of high temperature stress on growing stage and yield of rice in Jiang Su. Crops 2015, 2, 95–100. [Google Scholar]
  28. Sita, K.; Sehgal, A.; Hanumantharao, B.; Nair, R.M.; Prasad, P.V.V.; Kumar, S.; Gaur, P.M.; Farooq, M.; Siddique, K.H.M.; Varshney, R.K.; et al. Food legumes and rising temperatures: Effects, adaptive functional mechanisms specific to reproductive growth stage and strategies to improve heat tolerance. Front. Plant Sci. 2017, 8, 1658. [Google Scholar] [CrossRef]
  29. Ding, Y.; Wang, W.; Song, R.; Shao, Q.; Jiao, X.; Xing, W. Modeling spatial and temporal variability of the impact of climate change on rice irrigation water requirements in the middle and lower reaches of the Yangtze River, China. Agric. Water Manag. 2017, 193, 89–101. [Google Scholar] [CrossRef]
  30. National Bureau of Statistics of China. Statistical Yearbook of China; Statistical Press: Beijing, China, 2021. [Google Scholar]
  31. Ray, D.K.; Gerber, J.S.; Macdonald, G.K.; West, P.C. Climate variation explains a third of global crop yield variability. Nat. Commun. 2015, 6, 5989. [Google Scholar] [CrossRef]
  32. Espe, M.B.; Hill, J.E.; Hijmans, R.J.; Mckenzie, K.; Mutters, R.; Espino, L.A.; Leinfelder-Miles, M.; Van Kessel, C.; Linquist, B.A. Point stresses during reproductive stage rather than warming seasonal temperature determine yield in temperate rice. Glob. Change Biol. 2017, 23, 4386–4395. [Google Scholar] [CrossRef] [PubMed]
  33. China Meteorological Administration. China Meteorological Disaster Yearbook (2004–2019); Meteorological Press: Beijing, China, 2004–2019.
  34. Chen, S.X.; Wen, K.G. China Meteorological Disasters Book (Jiangsu, Zhejiang, Anhui, Jiangxi, Hubei and Hunan Provinces); Meteorogogical Press: Beijing, China, 2006. [Google Scholar]
  35. Kjeldsen, T.R.; Macdonald, N.; Lang, M.; Mediero, L.; Albuquerque, T.; Bogdanowicz, E.; Brázdil, R.; Castellarin, A.; David, V.; Fleig, A.; et al. Documentary evidence of past floods in Europe and their utility in flood frequency estimation. J. Hydrol. 2014, 517, 963–973. [Google Scholar]
  36. Petrović, A.M.; Dragićević, S.S.; Radić, B.P.; Milanović Pešić, A.Z. Historical torrential flood events in the Kolubara river basin. Nat. Hazards 2015, 79, 537–547. [Google Scholar] [CrossRef]
  37. Wu, X.; Wang, P.; Huo, Z.; Wu, D.; Yang, J. Crop Drought Identification Index for winter wheat based on evapotranspiration in the Huang-Huai-Hai Plain, China. Agric. Ecosyst. Environ. 2018, 263, 18–30. [Google Scholar] [CrossRef]
  38. Olesen, J.E.; Trnka, M.; Kersebaum, K.C.; Skjelvåg, A.O.; Seguin, B.; Peltonen-Sainio, P.; Rossi, F.; Kozyra, J.; Micale, F. Impacts and adaptation of European crop production systems to climate change. Eur. J. Agron. 2011, 34, 96–112. [Google Scholar] [CrossRef]
  39. GB/T 21985-2008; Temperature Index of High Temperature Harm for Main Crops. China Standards Press: Beijing, China, 2008.
  40. Luo, Q. Temperature thresholds and crop production: A review. Clim. Change 2011, 109, 583–598. [Google Scholar] [CrossRef]
  41. Zhang, Z.; Li, Y.; Chen, X.; Wang, Y.; Niu, B.; Liu, D.L.; He, J.; Pulatov, B.; Hassan, I.; Meng, Q. Impact of climate change and planting date shifts on growth and yields of double cropping rice in southeastern China in future. Agric. Syst. 2023, 205, 103581. [Google Scholar] [CrossRef]
  42. Wang, B.; Waters, C.; Orgill, S.; Cowie, A.; Clark, A.; Li Liu, D.; Simpson, M.; Mcgowen, I.; Sides, T. Estimating soil organic carbon stocks using different modelling techniques in the semi-arid rangelands of eastern Australia. Ecol. Indic. 2018, 88, 425–438. [Google Scholar]
  43. Hand, D.J. Measuring classifier performance: A coherent alternative to the area under the ROC curve. Mach. Learn. 2009, 77, 103–123. [Google Scholar] [CrossRef]
  44. Guo, A.; He, L.; Han, L.; Zhang, L. Construction of heat damage intensity index of early rice and its climate risk assessment. J. Nat. Disasters 2018, 27, 96–106. [Google Scholar]
  45. Prasanth, V.V.; Babu, M.S.; Basava, R.K.; Venkata, V.G.N.T.; Mangrauthia, S.K.; Voleti, S.R.; Neelamraju, S. Trait and marker associations in Oryza nivara and O. rufipogon derived rice lines under two different heat stress conditions. Front. Plant Sci. 2017, 8, 1819. [Google Scholar] [CrossRef]
  46. Oh-e, I.; Saitoh, K.; Kuroda, T. Effects of high temperature on growth, yield and dry-matter production of rice grown in the paddy field. Plant Prod. Sci. 2007, 10, 412–422. [Google Scholar] [CrossRef]
  47. Jagadish, S.V.; Muthurajan, R.; Oane, R.; Wheeler, T.R.; Heuer, S.; Bennett, J.; Craufurd, P.Q. Physiological and proteomic approaches to address heat tolerance during anthesis in rice (Oryza sativa L.). J. Exp. Bot. 2010, 61, 143–156. [Google Scholar] [PubMed]
  48. Shi, W.; Yin, X.; Struik, P.C.; Solis, C.; Xie, F.; Schmidt, R.C.; Huang, M.; Zou, Y.; Ye, C.; Jagadish, S.V.K. High day- and night-time temperatures affect grain growth dynamics in contrasting rice genotypes. J. Exp. Bot. 2017, 68, 5233–5245. [Google Scholar] [PubMed]
  49. Soda, N.; Gupta, B.K.; Anwar, K.; Sharan, A.; Govindjee; Singla-Pareek, S.L.; Pareek, A. Rice intermediate filament, OsIF, stabilizes photosynthetic machinery and yield under salinity and heat stress. Sci. Rep. 2018, 8, 4072. [Google Scholar] [CrossRef] [PubMed]
  50. Cao, Y.-Y.; Duan, H.; Yang, L.-N.; Wang, Z.-Q.; Liu, L.-J.; Yang, J.-C. Effect of high temperature during heading and early filling on grain yield and physiological characteristics in Indica rice. Acta Agron. Sin. 2009, 35, 512–521. [Google Scholar] [CrossRef]
  51. Aghamolki, M.T.K.; Yusop, M.K.; Oad, F.C.; Zakikhani, H.; Jaafar, H.Z.; Kharidah, S.; Musa, M.H. Heat stress effects on yield parameters of selected rice cultivars at reproductive growth stages. J. Food Agric. Environ. 2014, 12, 741–746. [Google Scholar]
  52. Xu, J.; Henry, A.; Sreenivasulu, N. Rice yield formation under high day and night temperatures—A prerequisite to ensure future food security. Plant Cell Env. 2020, 43, 1595–1608. [Google Scholar] [CrossRef]
  53. Kim, J.; Shon, J.; Lee, C.-K.; Yang, W.; Yoon, Y.; Yang, W.-H.; Kim, Y.-G.; Lee, B.-W. Relationship between grain filling duration and leaf senescence of temperate rice under high temperature. Field Crops Res. 2011, 122, 207–213. [Google Scholar] [CrossRef]
  54. Ishimaru, T.; Parween, S.; Saito, Y.; Shigemitsu, T.; Yamakawa, H.; Nakazono, M.; Masumura, T.; Nishizawa, N.K.; Kondo, M.; Sreenivasulu, N. Laser microdissection-based tissue-specific transcriptome analysis reveals a novel regulatory network of genes involved in heat-induced grain chalk in rice endosperm. Plant Cell Physiol. 2019, 60, 626–642. [Google Scholar] [CrossRef]
  55. Wada, T.; Miyahara, K.; Sonoda, J.Y.; Tsukaguchi, T.; Miyazaki, M.; Tsubone, M.; Ando, T.; Ebana, K.; Yamamoto, T.; Iwasawa, N.; et al. Detection of QTLs for white-back and basal-white grains caused by high temperature during ripening period in japonica rice. Breed Sci. 2015, 65, 216–225. [Google Scholar] [CrossRef] [PubMed]
  56. Zhang, Y.; Wang, P.; Chen, Y.; Yang, J.; Wu, D.; Ma, Y.; Huo, Z.; Liu, S. The optimal time-scale of Standardized Precipitation Index for early identifying summer maize drought in the Huang-Huai-Hai region, China. J. Hydrol. Reg. Stud. 2023, 46, 101350. [Google Scholar]
  57. Yang, J.; Dong, H.; Huo, Z.; Wang, P.; Yao, S.; Wu, D.; Ma, Y. Threshold-based characteristics of apricot frost exposure at young fruit in the warm temperate zone, China. Int. J. Climatol. 2021, 42, 1460–1471. [Google Scholar] [CrossRef]
  58. Tang, J.; Wang, P.; Li, X.; Yang, J.; Wu, D.; Ma, Y.; Li, S.; Jin, Z.; Huo, Z. Disaster event-based spring frost damage identification indicator for tea plants and its applications over the region north of the Yangtze River, China. Ecol. Indic. 2023, 146, 109912. [Google Scholar]
  59. Kim, D.-H.; Jang, T.; Hwang, S.; Jeong, H. Paddy rice adaptation strategies to climate change: Transplanting date shift and BMP applications. Agric. Water Manag. 2021, 252, 106926. [Google Scholar] [CrossRef]
  60. Li, T.; Hasegawa, T.; Yin, X.; Zhu, Y.; Boote, K.; Adam, M.; Bregaglio, S.; Buis, S.; Confalonieri, R.; Fumoto, T.; et al. Uncertainties in predicting rice yield by current crop models under a wide range of climatic conditions. Glob. Change Biol. 2015, 21, 1328–1341. [Google Scholar] [CrossRef]
  61. Shah, F.; Nie, L.; Cui, K.; Shah, T.; Wu, W.; Chen, C.; Zhu, L.; Ali, F.; Fahad, S.; Huang, J. Rice grain yield and component responses to near 2 °C of warming. Field Crops Res. 2014, 157, 98–110. [Google Scholar] [CrossRef]
  62. Kim, H.Y.; Ko, J.; Kang, S.; Tenhunen, J. Impacts of climate change on paddy rice yield in a temperate climate. Glob. Change Biol. 2013, 19, 548–562. [Google Scholar] [CrossRef]
  63. Wang, H.; Chen, W.; Eggert, K.; Charnikhova, T.; Bouwmeester, H.; Schweizer, P.; Hajirezaei, M.R.; Seiler, C.; Sreenivasulu, N.; Von Wirén, N.; et al. Abscisic acid influences tillering by modulation of strigolactones in barley. J. Exp. Bot. 2018, 69, 3883–3898. [Google Scholar] [CrossRef]
  64. Hussien, A.; Tavakol, E.; Horner, D.S.; Muñoz-Amatriaín, M.; Muehlbauer, G.J.; Rossini, L. Genetics of tillering in rice and barley. Plant Genome 2014, 7, 32. [Google Scholar] [CrossRef]
  65. Liu, X.; Hu, Q.; Yan, J.; Sun, K.; Liang, Y.; Jia, M.; Meng, X.; Fang, S.; Wang, Y.; Jing, Y.; et al. ζ-Carotene Isomerase Suppresses Tillering in Rice through the Coordinated Biosynthesis of Strigolactone and Abscisic Acid. Mol. Plant 2020, 13, 1784–1801. [Google Scholar] [CrossRef] [PubMed]
  66. Sharma, R.; De Vleesschauwer, D.; Sharma, M.K.; Ronald, P.C. Recent advances in dissecting stress-regulatory crosstalk in Rice. Mol. Plant 2013, 6, 250–260. [Google Scholar] [CrossRef] [PubMed]
  67. Chinnusamy, V.; Gong, Z.; Zhu, J.-K. Abscisic Acid-mediated Epigenetic Processes in Plant Development and Stress Responses. J. Integr. Plant Biol. 2008, 50, 1187–1195. [Google Scholar] [CrossRef]
  68. Huo, Z.; Zhang, L.; Kong, R.; Jiang, M.; Zhang, H. The agro-climatic change characteristics across China during the latest decades. Agriculture 2022, 12, 147. [Google Scholar] [CrossRef]
  69. Estrella, N.; Sparks, T.H.; Menzel, A. Trends and temperature response in the phenology of crops in Germany. Glob. Change Biol. 2007, 13, 1737–1747. [Google Scholar] [CrossRef]
  70. Chaturvedi, A.K.; Bahuguna, R.N.; Shah, D.; Pal, M.; Jagadish, S.V.K. High temperature stress during flowering and grain filling offsets beneficial impact of elevated CO2 on assimilate partitioning and sink-strength in rice. Sci. Rep. 2017, 7, 8227. [Google Scholar] [CrossRef]
  71. Ziska, L.H.; Manalo, P.A.; Ordonez, R.A. Intraspecific variation in the response of rice (Oryza sativa L.) to increased CO2 and temperature: Growth and yield response of 17 cultivars. J. Exp. Bot. 1996, 47, 1353–1359. [Google Scholar] [CrossRef]
  72. Vu, J.C.V.; Jr, L.H.A.; Boote, K.J.; Bowes, G. Effects of elevated CO2 and temperature on photosynthesis and Rubisco in rice and soybean. Plant Cell Environ. 1997, 20, 68–76. [Google Scholar] [CrossRef]
Figure 1. Location of the study region and the distribution of meteorological stations.
Figure 1. Location of the study region and the distribution of meteorological stations.
Agronomy 13 02574 g001
Figure 2. Detailed distribution of Tmax values in H and NH databases for single-season rice. (ad) are tillering–jointing, booting, flowering, and filling stages, respectively; NH−5 and NH+5 refer to non-heat samples of the prior 5 days and the behindhand 5 days, respectively; white dots refer to the mean values of Tmax for each sample type.
Figure 2. Detailed distribution of Tmax values in H and NH databases for single-season rice. (ad) are tillering–jointing, booting, flowering, and filling stages, respectively; NH−5 and NH+5 refer to non-heat samples of the prior 5 days and the behindhand 5 days, respectively; white dots refer to the mean values of Tmax for each sample type.
Agronomy 13 02574 g002
Figure 3. IF between the accumulated temperature with 11 test thresholds and yield reduction rate for single-season rice. (ad) are tillering–jointing, booting, flowering and filling stages, respectively; the red triangles refer to the first three most important scores.
Figure 3. IF between the accumulated temperature with 11 test thresholds and yield reduction rate for single-season rice. (ad) are tillering–jointing, booting, flowering and filling stages, respectively; the red triangles refer to the first three most important scores.
Agronomy 13 02574 g003
Figure 4. Overall accuracy with 11 test thresholds discriminating between H and NH databases for single-season rice.
Figure 4. Overall accuracy with 11 test thresholds discriminating between H and NH databases for single-season rice.
Agronomy 13 02574 g004
Figure 5. ROC curve with 11 test thresholds for single-season rice. (ad) The tillering–jointing, booting, flowering and filling stages, respectively; points with the first three key thresholds by importance analysis are marked red in the figure.
Figure 5. ROC curve with 11 test thresholds for single-season rice. (ad) The tillering–jointing, booting, flowering and filling stages, respectively; points with the first three key thresholds by importance analysis are marked red in the figure.
Agronomy 13 02574 g005
Figure 6. Temporal evolution characteristics of Tmax during a multi-stage heat event in the southeast region of HB province. The red lines with values of 36, 35, and 38 °C are used as the baseline for heat occurrence at different phenological stages proposed by corresponding critical thresholds, respectively; the grey-shaded area is the period of actual record for single-season rice heat stress; each icon refers to the data at one meteorological station, for a total of 21 stations.
Figure 6. Temporal evolution characteristics of Tmax during a multi-stage heat event in the southeast region of HB province. The red lines with values of 36, 35, and 38 °C are used as the baseline for heat occurrence at different phenological stages proposed by corresponding critical thresholds, respectively; the grey-shaded area is the period of actual record for single-season rice heat stress; each icon refers to the data at one meteorological station, for a total of 21 stations.
Agronomy 13 02574 g006
Figure 7. Spatial distribution of average accumulated harmful temperature (Tcum) and number of heat days (HD) from 1971 to 2020 in MLRYR. (ad) refer to Tcums at tillering–jointing, booting, flowering and filling, and (eh) refer to HDs at tillering–jointing, booting, flowering and filling, respectively.
Figure 7. Spatial distribution of average accumulated harmful temperature (Tcum) and number of heat days (HD) from 1971 to 2020 in MLRYR. (ad) refer to Tcums at tillering–jointing, booting, flowering and filling, and (eh) refer to HDs at tillering–jointing, booting, flowering and filling, respectively.
Agronomy 13 02574 g007
Figure 8. Fluctuation of accumulated harmful temperature (Tcum) and number of heat days (HD) from 1971 to 2020 in MLRYR.
Figure 8. Fluctuation of accumulated harmful temperature (Tcum) and number of heat days (HD) from 1971 to 2020 in MLRYR.
Agronomy 13 02574 g008
Figure 9. MK results for accumulated harmful temperature (Tcum, (a)) and number of heat days (HD, (b)) trends from 1971 to 2020 in MLRYR.
Figure 9. MK results for accumulated harmful temperature (Tcum, (a)) and number of heat days (HD, (b)) trends from 1971 to 2020 in MLRYR.
Agronomy 13 02574 g009
Figure 10. Mean trends of accumulated harmful temperature (Tcum) and number of heat days (HD) in 1971–2000, 2001–2009, and 2010–2020 for single-season rice heat stress. Blue and red asterisks both refer to abnormal values.
Figure 10. Mean trends of accumulated harmful temperature (Tcum) and number of heat days (HD) in 1971–2000, 2001–2009, and 2010–2020 for single-season rice heat stress. Blue and red asterisks both refer to abnormal values.
Agronomy 13 02574 g010
Figure 11. Spatial distribution of first heat date (FHD, (a)) and last heat date (LHD, (b)) in MLRYR.
Figure 11. Spatial distribution of first heat date (FHD, (a)) and last heat date (LHD, (b)) in MLRYR.
Agronomy 13 02574 g011
Table 1. Information on meteorological, phenology and disaster data used in this study.
Table 1. Information on meteorological, phenology and disaster data used in this study.
ClassificationData IndexSourcePeriodArea Scope
MeteorologicalDaily maximum temperatureNational Meteorological
Information Center
1971–2020501 stations
PhenologySeeding, tillering, jointing, booting, flowering and filling date of single-season riceAgro-meteorological experimental station1981–2010501 meteorological stations interpolated from phenology data in 34 stations
YieldYield reduction rate (YRR) of single-season riceNational Bureau of Statistics1971–2020Six provinces (JS, ZJ, AH, JX, HB and HN)
DisasterRecords of heat stress process of single-season rice China Meteorological Disasters Book》, 《Yearbook of
Meteorological Disasters in
China
1971–2000,
2004–2019
Six provinces (JS, ZJ, AH, JX, HB and HN)
Table 2. Statistics of Tmax values in H and NH databases for single-season rice.
Table 2. Statistics of Tmax values in H and NH databases for single-season rice.
Phenology Database TypeMinimumMaximumMeanStandard Deviation
Tillering–jointing H2340.833.693.65
NH22.237.430.303.08
Booting,H28.141.736.311.98
NH21.938.331.623.32
FloweringH24.842.436.432.25
NH21.436.830.683.41
FillingH23.343.236.822.68
NH19.739.933.153.60
Table 3. Detailed statistics of Overall Accuracy and ROC curves in the H and NH databases. (TP and FP represent the number of rice heat stress in the H database that are retrieved correctly and incorrectly, respectively; TN and FN represent the number of non-heat samples in the NH database that are retrieved correctly and incorrectly, respectively; TPR and FPR represent the proportion of TP to all positive observations (TP + FN) and FP to all negative observations (TN + FP), respectively.).
Table 3. Detailed statistics of Overall Accuracy and ROC curves in the H and NH databases. (TP and FP represent the number of rice heat stress in the H database that are retrieved correctly and incorrectly, respectively; TN and FN represent the number of non-heat samples in the NH database that are retrieved correctly and incorrectly, respectively; TPR and FPR represent the proportion of TP to all positive observations (TP + FN) and FP to all negative observations (TN + FP), respectively.).
Phenology Test Threshold (°C)TPTNFNFPOverall AccuracyTPRFPR
Tillering–jointing 30122302410.34210.988
321225701870.48910.766
36122235090.97510.037
Booting,30108602100.35210.972
31108902070.36110.958
351081710450.86110.208
Flowering301484602500.43710.845
311486502310.48010.780
351482530430.90310.145
Filling31237704670.34310.992
3723735601180.83410.249
3823437331010.85410.213
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Jiang, M.; Huo, Z.; Zhang, L.; Kong, R.; Li, M.; Mi, Q. Characteristic Identification of Heat Exposure Based on Disaster Events for Single-Season Rice along the Middle and Lower Reaches of the Yangtze River, China. Agronomy 2023, 13, 2574. https://doi.org/10.3390/agronomy13102574

AMA Style

Jiang M, Huo Z, Zhang L, Kong R, Li M, Mi Q. Characteristic Identification of Heat Exposure Based on Disaster Events for Single-Season Rice along the Middle and Lower Reaches of the Yangtze River, China. Agronomy. 2023; 13(10):2574. https://doi.org/10.3390/agronomy13102574

Chicago/Turabian Style

Jiang, Mengyuan, Zhiguo Huo, Lei Zhang, Rui Kong, Meixuan Li, and Qianchuan Mi. 2023. "Characteristic Identification of Heat Exposure Based on Disaster Events for Single-Season Rice along the Middle and Lower Reaches of the Yangtze River, China" Agronomy 13, no. 10: 2574. https://doi.org/10.3390/agronomy13102574

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop