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. 2014 Nov 16;2014:308042. doi: 10.1155/2014/308042

Heritability and Genetic Advance among Chili Pepper Genotypes for Heat Tolerance and Morphophysiological Characteristics

Magaji G Usman 1, M Y Rafii 1,2,*, M R Ismail 1,2, M A Malek 2,3, Mohammad Abdul Latif 1,4
PMCID: PMC4248334  PMID: 25478590

Abstract

High temperature tolerance is an important component of adaptation to arid and semiarid cropping environment in chili pepper. Two experiments were carried out to study the genetic variability among chili pepper for heat tolerance and morphophysiological traits and to estimate heritability and genetic advance expected from selection. There was a highly significant variation among the genotypes in response to high temperature (CMT), photosynthesis rate, plant height, disease incidence, fruit length, fruit weight, number of fruits, and yield per plant. At 5% selection intensity, high genetic advance as percent of the mean (>20%) was observed for CMT, photosynthesis rate, fruit length, fruit weight, number of fruits, and yield per plant. Similarly, high heritability (>60%) was also observed indicating the substantial effect of additive gene more than the environmental effect. Yield per plant showed strong to moderately positive correlations (r = 0.23–0.56) at phenotypic level while at genotypic level correlation coefficient ranged from 0.16 to 0.72 for CMT, plant height, fruit length, and number of fruits. Cluster analysis revealed eight groups and Group VIII recorded the highest CMT and yield. Group IV recorded 13 genotypes while Groups II, VII, and VIII recorded one each. The results showed that the availability of genetic variance could be useful for exploitation through selection for further breeding purposes.

1. Introduction

Chili pepper (Capsicum annuum L. and Capsicum frutescence L.) is widely cultivated, primarily as a spice crop [1]. The optimum day temperatures for chili pepper growth range from 20 to 30°C [2], and day temperatures rise above 30°C year round in Malaysia [3]. The domestic production of chili pepper in Malaysia can hardly meet 70% of demand due to poor performance of local varieties under high temperature. Furthermore, high temperature is one of the major problems for chili cultivation in Malaysia. Such conditions are the important factors limiting the production of chili pepper. Therefore, understanding the effect and mechanism of high temperature on chili pepper are the important factors for the improvement of the quality of the crop. However, chili pepper, as well as other crops such as groundnut [4] and heat tolerant genotypes will be needed to sustain their production under high temperature environments.

Yield is a determining factor for crop improvement [5]. Chili pepper, as in other crops, yield is a quantitative trait that is influenced by a number of yield contributing parameters. The selection of desirable genotypes is usually based on yield and yield components. It is therefore necessary to study the mutual relationship between yield and yield components for efficient utilization of the genetic stock in crop improvement program of chili pepper. Variability in plants is the first step in understanding how to improve or produce new plants. Heritability is the degree of genetic control associated to some important traits [6]. It indicates how much of the genetic variability has a genetic origin and gives necessary information for the genetic selection process [7]. To improve grain yield potentials of crops in any breeding programs, it is necessary to obtain adequate information on the magnitude and type of genetic variability and their corresponding heritability. This is because selection of superior genotypes is proportional to the amount of genetic variability present and the extent to which the characters are inherited. Heritability is used to indicate the relative degree to which a character is transmitted from parent to offspring. The magnitude of such estimates also suggests the extent to which improvement is possible through selection [5].

Temperature and other abiotic stresses are clearly limiting factors for the growth and development of crop. Indeed stresses due to high temperature can be harmful to all phases of plant development, and global climate change is thought to cause extreme environmental fluctuations in most agricultural regions [8]. Temperature increment due to changing climatic condition is a serious threat [9] which affects crop production. So, understanding how the plants respond to stress is a challenging area of research [10]. Cell membrane thermostability (CMT) is a phenotypic parameter used in measuring electrolyte leakage from leafs of plants at different temperatures. CMT is a very sensitive and rapid method to identify heat tolerance in plants [11]. Several studies have indicated that CMT is effective in detecting genetic difference among several crops for heat tolerance [12, 13]. However, the mechanism for heat tolerance using the electrolyte leakage of crops under heat stress need to be more exploited in order to identify heat tolerant lines for the development of high yielding heat tolerant hybrid varieties, which will contribute to achieve self-sufficiency in chili production in Malaysia. Genotypes within several crop species are found to differ with respect to heat tolerance, where heat tolerant genotypes are referred to as giving the highest yield under high temperature condition [1416]. Heat tolerance can be referred to as performance of a plant with respect to its yield or physiological processes under elevated temperature as compared with its performance under optimal temperature [17]. Genotypic differences in tolerance/susceptibility have been reported in chili pepper for pollen tube length and pollen germination and membrane stability [18, 19]. However, only a very limited number of genotypes of chili pepper have being studied. Furthermore, association between heat tolerance and cell membrane thermostability with respect to selection criteria for breeding purposes has not been investigated.

The objectives of this research was to identify chili pepper genotypes tolerant to high temperature and study the genotypic variation among the genotypes for heat tolerance and other yield related traits, to determine whether genotypic differences in tolerance to high temperature were associated with membrane thermostability, to study the correlation between heat tolerance and morpho-physiological traits and determine whether heat tolerance can be used as selection criteria in chili pepper breeding program.

2. Materials and Methods

2.1. Site and Location

This research was conducted between May and August 2013 using the Rain Shelter facility of the Agro-technology experimental site, Institute of Tropical Agriculture, Universiti Putra Malaysia. It is located on 3°02′ N latitude and 101°42′ East longitude and altitude is 31 m above sea level. The average climatic conditions are represented in Table 1.

Table 1.

The average temperature, solar radiation, and rainfall of the experimental site during the period of the experiment (2013/2014).

Months Temperature (°C) Solar radiation MJ/m² Rainfall (mm)
Maximum Minimum
May 38.5 24.5 22.70
June 36.3 24.2 21.2 4.2
July 36.3 23.8 20.20 100
August 39.3 23.8

2.2. Plant Husbandry

Experiment was carried out in a prepared polythene bag under rain shelter condition. All genotypes used for this experiment were collected from Asian Vegetable Research and Development Centre, AVRDC, in Taiwan, except for Kulai, which is a local variety cultivated in Malaysia (Table 2). Thirty-six genotypes belonging to two species of Capsicum were sown in seed trays on 8th May, 2013, with 1-2 seeds per cell and the growing medium was peat moss. They were later transplanted to the pots filled with cocoa peat. The pots were 17 cm × 30 cm with small holes to drain excess water. The experiment was laid in a randomized complete block design (RCBD) in three replications. Two pots were assigned for each genotype in each replication (72 pots per replication). The pots were oriented east to west and spaced 75 cm × 150 cm. Seedling emerged within 7–10 days after sowing and were transplanted 4 weeks after sowing. All pots were irrigated and fertilized using fertigation system of cropping with drip system of irrigation.

Table 2.

List of chili pepper genotypes and their pedigree, specie, and heat tolerance used in this experiment.

Genotype Source Specie Pedigree Heat tolerancea
AVPP9703 CCA 1410A C. annuum HDA210/Szechwan10/MC4 excellent
AVPP9901 CCA 3106 C. annuum HM-19/155-42//G-4 good
AVPP9806 CCA 196-A C. annuum SlamChiliF1/HDA248 b
AVPP9813 CCA 323 C. Frutescens Kulim/HDA295 (Berke's Joy) excellent
AVPP0002 CCA 3331 C. annuum Arunalu/Tumpang excellent
AVPP0012 Jin's Joy C. annuum Jin's Joy fair
AVPP0102 CCA 3636 C. annuum IR/LongFruit excellent
AVPP0004 Maor/Perennial C. frutescens Maor/Perennial good
AVPP0104 CCA 3468 C. annuum MI-2/Taiwan83-168-1-1//MI-2 good
AVPP0105 CCA 321 C. annuum Kulim/HDA248 excellent
AVPP9905 Susan's Joy C. annuum Susan's Joy excellent
AVPP9815 CCA226A-3 C. frutescens Corbadzijiski/HDA248
AVPP0201 CCA 4283 C. annuum (Szechwan9/PerennialHDV)/Jin's Curlicue//F1 Hy Hot 3 F3 sel.
AVPP0116 CCA 3743 C. annuum PSP-11/Jin's Delight//Kulai excellent
AVPP9805 CCA 2345 C. annuum HDA248/5*LongFruitA
AVPP0109 MSH-1 seln C. annuum F1 MSH-1 excellent
AVPP0305 CCA 4824 C. frutescens PBC325/PBC308
AVPP0101 CCA 3617 C. annuum FriesdorferSelex/LongFruit excellent
AVPP0805 CCA6306-1-3-3-3-1 C. annuum Jatilaba/CCA321//Jatilaba
AVPP0307 CCA 4860 C. annuum LongThick/9852-173
AVPP0506 CCA5213 C. frutescens PBC 481 sel.//Kulium/HDA248
AVPP0803 CCA6875-1-1-3-1-3 C. annuum Var F/UF8752-3
AVPP0907 C. annuum Kulim/HDA248//Lorai
AVPP0306 CCA 4851 C. annuum VC232/9945-1856
AVPP0804 CCA6875-8-1-3-1-1 C. annuum Var F/UF8752-3
AVPP0512 CCA5217 C. frutescens Jin's Joy//Kulium/HDA248
AVPP0514 CCA5218 C. annuum Jin's Joy//Kulai*3/PBC932
AVPP0702 CCA6023-9-1-1-2-1 C. annuum Jin's Joy/4/Bangchang-selex///HDA210/Szechwan10//MC4
AVPP0103 CCA 260 C. annuum Szechwan9/Perennial excellent
AVPP0014 Mr. Lee No.3 seln C. annuum Mr. Lee No.3 selex fair
AVPP0705 CCA5684-05-1-2-1-1 C. frutescens SSK-1/0209-4//SSK-1/PBC495
AVPP0904 C. annuum Jin's Joy//Kulim/HDA248/Jin's Joy//Kulim/HDA248
AVPP0513 CCA5218 C. frutescens Jin's Joy//Kulai*3/PBC932
AVPP9812 CCA 336-B C. frutescens PBC385/HDA248 fair
C05573 PBC 142 C. annuum Pant C-1 (long term ck.) good
Kulai Local C. annuum

aAVRDC, unpublished data.

bData not available.

2.3. Procedure for Cell Membrane Thermostability

The membrane stability test was conducted at the Plant Physiology laboratory, Department of Crop Science, Universiti Putra Malaysia. The leaf cell membrane thermostability (CMT) in the chili pepper genotypes was assessed according to the procedure described [20]. A sample for assay consists of a paired set, namely, control (C) and treatment (T) set of 6 leaf disks each 1.3 cm2. The disks were cut from five fully expanded 3rd or 4th leaves from the top of the stem axis from each genotype. Samples were replicated three times each. Prior to assay, the paired set of leaf disks were placed in two separate test tubes (50 mL) and washed thoroughly with four exchanges of de-ionized water, 10 mL each time, to remove electrolytes adhering to the cut surface of the leaf discs. After the final wash, both sets of test tubes were filled with 10 mL de-ionized water and sealed with aluminium foil to avoid evaporation. The T set of the test tubes were incubated for 20 min at 50°C in a temperature controlled water bath, while the C set of test tubes were kept at room temperature (approximately 25°C). Both sets of test tubes were then incubated at 4°C (kept in a refrigerator) for 24 hrs. Initial conductance reading of both sets (CEC 1 and TEC 1) was made using an electrical conductivity meter (Starter) after bringing test tubes to room temperature. Tubes were then sealed again with aluminium foil and autoclaved at 121°C and 0.15 MPa for 20 min. to completely kill the leaf tissue. Autoclaved tubes were cooled to room temperature; content was mixed thoroughly and final conductance (CEC 2 and TEC 2) reading was taken. The CMT was calculated using the following equation, where TEC and CEC are a measure of conductance in treated and control test tubes, respectively, at initial (CEC 1 and TEC 1) and final (CEC 2 and TEC 2) conductance measurements [19]:

CMT(%)=1TEC1/TEC21(CEC1/CEC2)×100. (1)

2.4. Morpho-Physiological Parameters

Characters assessed include disease incidence (%), plant height (cm), days to flowering, fruit length (cm), fruit weight (g), number of fruits, yield per plant (g), chlorophyll content, photosynthesis rate, and degree of pungency.

2.5. Chlorophyll Determination

Measurement of chlorophyll content was done following [21] procedure. Fresh leaves were collected from each replication from each genotype. One cm2 leaf disks were cut from the leaves using leaf puncher and were transferred immediately into scintillation vials containing 20 mL of 80% acetone. The vials were capped and covered with aluminium foil after which kept in the dark for 7 days. UV spectrophotometer was used to measure the absorbance at 647 and 664 nm wavelengths. Using the following formulas, total actual chlorophyll was calculated:

Chlorophyll  a=13.19×A6642.57×A647,Chlorophyll  b=22.1×A6475.26×A664,Total  chlorophyll=Chlorophyll  a+chlorophyll  b,Actual  chlorophyll=3.5×total  chlorophyll1. (2)

2.6. Photosynthesis Rate (µmol/m2/s) Measurement

Net photosynthetic for the 36 genotypes was measured from the leaves of 90-day-old seedlings. The uppermost expanded leaves were selected for the measurement using an LI-6400XT portable photosynthesis system (LiCOR Inc., Lincoln, Nebraska, USA).

2.7. Degree of Pungency

The extractions of capsaicin from the chili pepper samples was done using the method described [22] and were analyzed using Ultra Fast Liquid Chromatography (UFLC) as described [23]. Whole chili fruits from the 36 genotypes were collected for determining degree of pungency (spicy level). Scoville Heat Units was used to calculate the heat units for all samples. Scoville Heat Units are calculated in parts per million of heat (ppmH) based on sample dry weight according to the following formula from [24]:

ppmH=Peak  area  of  capsaicin+0.82peak  area  of  dihydrocapsaicin×ppm  standardmL  acetonitrile×Total  capsaicin  peak  area  of  standardg  sample1. (3)

Conversion to Scoville Heat Units was made by multiplying ppmH by a factor of 15. They are classified as follows:

  1. (0–700 SHU) nonpungent

  2. (700–3,000 SHU) mildly pungent

  3. (25,000–70,000 SHU) highly pungent

  4. (3,000–25,000 SHU) moderately pungent

  5. (>80,000 SHU) very highly pungent [25].

2.8. Statistical Analysis

Results were analyzed using SAS software (version 9.1) for all traits and means were separated using Duncan's Multiple Range Test (DMRT) and Least Significance Difference (LSD) at 5% level.

2.8.1. Phenotypic and Genotypic Coefficient of Variation

The estimates of phenotypic and genotypic coefficient of variation were calculated as described [26] as follows:

PCV(%)=Vpmean×100,GCV(%)=Vgmean×100, (4)

where PCV is phenotypic coefficient of Variance, VP is phenotypic variance, GCV is Genotypic Coefficient of Variance, and Vg is genotypic variance. GCV and PCV values were categorized as low (0–10%), moderate (10–20%), and high (20% and above) as indicated by [27, 28].

2.8.2. Heritability

It was estimated as the ratio of total genotypic variance to the phenotypic variance according to [7]:

H2=VgVp×100, (5)

where H 2 = % Broad sense heritability. The heritability percentage was categorized as low (0–30%), moderate (30–60%), and high ≥60% as given by [29].

2.8.3. Genetic Advance

The extent of genetic advance expected through selection for the character was calculated as in [29]:

Genetic  Advance  GA:H×P×K, (6)

where H is heritability, P is phenotypic standard deviation, and K is selection deferential (2.06 at 5%).

Genetic Gain (%) = GA × 100; it is categorized as low (0–10%), moderate (10–20%) and high (20% and above) [29].

2.9. Multivariate Analysis

Cluster and Principal Component Analysis were carried out to assess the genetic diversity of cell membrane thermostability and yield characters using NTSYS-pc software (version 2.1). Data were analyzed based on Euclidian distance method, dissimilarity coefficient. In order to determine the genetic relationships among the chili pepper accessions the UPGMA algorithm and SAHN clustering were applied. The PCA of the 36 chili pepper genotypes were calculated by EIGEN module of NTSYS-pc software.

3. Results

3.1. Cell Membrane Thermostability (CMT)

Looking at the climatic condition at which the plants were grown, cell membrane thermostability would prove effective for screening the genotypes for heat tolerance. The result from this study showed that there was a highly significant (P < 0.01) difference among the genotypes in the relative injury (RI) and cell membrane thermostability (CMT) (Table 3). The cell membrane thermostability values ranged from 11.70 (AVPP9901) to 89.27% (AVPP0702) with a mean value of 64.62%. Most of the genotypes were recorded with high CMT values (>60%). Genotypes AVPP0105, AVPP9905, AVPP0116, AVPP0506, AVPP0803, C05573, AVPP0014, AVPP0702, AVPP0513, and AVPP0904 were found to be the most heat tolerant with the highest CMT values, while genotypes AVPP9703, AVPP9901, and AVPP0002 recorded the lowest CMT values indicating sensitivity to heat at 50°C.

Table 3.

Relative injury as determined by cell membrane thermostability test at 25 and 50°C for 20 min for 36 genotypes of Capsicum spp.

GENOTYPE Relative injury (%) CMT (%)v
25°Ca 50°Ca Injury*
AVPP9703 31.00 89.00 84.13 15.87
AVPP9901 26.33 91.2 88.30 11.70
AVPP9806 18.57 59.07 50.00 50.00
AVPP9813 22.00 62.10 51.03 48.97
AVPP0002 28.67 86.83 81.57 18.43
AVPP0012 22.07 81.23 75.77 24.23
AVPP0102 31.70 84.10 76.33 23.67
AVPP0004 23.53 56.93 43.27 56.73
AVPP0104 23.40 71.30 62.40 37.60
AVPP0105 25.23 38.57 17.67 82.33
AVPP9905 29.63 40.20 14.90 85.10
AVPP9815 30.93 68.43 54.20 45.80
AVPP0201 32.83 47.97 22.20 77.80
AVPP0116 32.67 40.90 11.97 88.0
AVPP9805 27.07 56.90 41.03 58.97
AVPP0109 36.03 61.40 39.03 60.97
AVPP0305 31.93 45.23 18.97 81.03
AVPP0101 42.47 68.50 45.63 54.37
AVPP0805 21.67 36.40 18.67 81.33
AVPP0307 23.20 43.03 25.90 74.10
AVPP0506 34.63 42.23 11.90 88.10
AVPP0803 21.50 34.20 15.87 84.13
AVPP0907 32.33 32.33 29.97 69.73
AVPP0306 26.27 49.07 30.83 69.17
AVPP0804 26.73 46.67 27.30 72.70
AVPP0512 23.40 39.27 20.67 79.33
AVPP0514 28.43 49.20 29.03 70.97
AVPP0702 33.20 40.43 10.73 89.27
AVPP0103 31.83 44.97 18.80 81.20
AVPP0014 27.20 35.40 11.57 88.43
AVPP0705 28.70 48.10 27.27 72.73
AVPP0904 27.23 39.20 16.50 83.50
AVPP0513 37.17 46.27 13.43 86.57
AVPP9812 29.80 43.37 19.37 80.63
C05573 25.97 38.47 17.03 82.97
Kulai 21.37 60.93 50.13 49.87

Means 28.24 53.92 35.37 64.62
LSD (P < 0.05) 7.39 11.95 17.43 17.39
SEM 0.61 1.67 2.37 2.37

Mean values were separated using Least Significance Difference at 5% level of probability.

aCalculated as (initial conductivity/final conductivity) × 100.

*Calculated as calibrated RI = {1 − [1 − (TEC1/TEC2)]/[1 − (CEC1/CEC2)]}  × 100.

vCalculated as [1 − (TEC1/TEC2)]/[1 − (CEC1/CEC2)] × 100.

LSD = Least significance difference.

SEM = Standard error of mean.

3.2. Morphophysiological Characters

All the morphophysiological characters studied in this experiment showed highly significant (P < 0.01) difference except days to flowering and chlorophyll content (Table 4). The means for the 9 traits are presented in Table 5. The yield per plant ranged from 108.69 (AVPP0804) to 1144.3 g (AVPP9905). The plant height at harvest ranged from 41.4 to 92.13 cm which were recorded by AVPP0804 and AVPP0116 genotypes, respectively (Table 5). Significant range of variations was also observed for plant height at harvest, disease incidence, fruit length, fruit weight, and number of fruits. Similarly, a highly significant (P < 0.01) variation was observed among the 36 genotypes for photosynthesis rate and degree of pungency. The genotype Kulai recorded the highest rate of photosynthesis (19.32) while AVPP0705 gave the lowest (3.75). The average rate of photosynthesis in this investigation was to be 13.29 µmol/m2/s. Degree of pungency or spicy level of the chili were found to vary significantly (P < 0.01) among the genotypes (Table 4). The genotype AVPP0705 showed the highest pungency (247245.28 SHU). The capsaicin and dihydrocapsaicin contents ranged from 175.26 to 133.1 mg/L, respectively (Table 6). However, no significant variation was observed for chlorophyll content and days to flowering.

Table 4.

Analysis of variance for 11 characters for the 36 Capsicum spp.

Traits Genotype (DF = 35) Error (DF = 70) CV (%)
PLH6WK 200.00* 113.50 24.09
PLHH 478.23** 102.28 14.55
Days to flowering 19.90ns 16.24 6.31
Disease incidence 524.02* 318.52 49.07
Chlorophyll content 5.56ns 5.99 37.23
Photosynthesis rate 37.97** 0.0016 0.305
Fruit length 18.64** 2.73 14.26
Fruit weight 161.95** 3.84 20.45
Number of fruits 6456.66** 1385.09 46.42
Yield 146873** 50594.56 49.59
Membrane stability 1622.85** 112.73 16.43
SHUs 4945258353.7** 7448153.84 7.30

*Significant at 5%, **highly significant at 1%, ns = not significant, PLHH: plant height at harvest, PLH6WK: plant height at 6 weeks after transplanting, SHUs = Scoville heat units.

Table 5.

Means for 10 characters studied in 36 genotypes of Capsicum spp.

Genotype PH6WK PLHH DF DI (%) CPL Photo FL (cm) FW (g) NF Y (g/pl)
AVPP9703 45.07 60.60 63.00 31.25 5.64 14.28 10.79 9.08 49.33 338.08
AVPP9901 32.15 47.10 68.50 78.89 6.43 10.92 8.28 6.07 62.00 299.36
AVPP9806 41.25 77.87 60.67 31.59 6.30 15.24 13.41 10.93 47.00 332.37
AVPP9813 56.33 72.07 61.67 30.73 5.75 12.22 10.73 9.43 78.00 554.79
AVPP0002 37.62 60.23 62.83 40.79 6.30 10.92 9.09 3.29 208.33 490.44
AVPP0012 44.80 77.60 67.00 49.10 7.35 15.24 13.16 8.08 20.00 102.03
AVPP0102 56.73 74.23 61.75 39.53 9.65 12.22 12.37 10.30 61.67 574.83
AVPP0004 43.47 77.07 65.00 38.85 4.60 10.92 9.19 6.03 86.67 479.63
AVPP0104 40.85 59.13 60.50 9.11 7.01 15.24 8.72 2.34 150.33 385.10
AVPP0105 39.50 78.57 63.00 40.37 5.91 12.22 12.31 9.67 142.33 813.79
AVPP9905 43.97 68.27 62.67 41.24 5.57 12.74 16.43 22.94 63.00 1144.30
AVPP9815 27.43 50.93 62.33 36.71 7.43 14.58 9.76 6.03 61.67 329.39
AVPP0201 45.23 59.40 60.67 29.80 7.61 11.48 11.71 6.19 78.67 407.36
AVPP0116 60.75 92.13 64.50 28.14 5.60 17.62 10.55 11.65 46.33 411.35
AVPP9805 28.43 45.37 65.00 28.83 7.90 13.56 15.35 14.67 21.00 282.83
AVPP0109 40.07 66.67 63.83 41.86 7.07 16.93 11.29 4.27 130.33 487.72
AVPP0305 55.10 67.30 59.00 30.47 7.92 10.47 12.91 9.73 116.00 711.27
AVPP0101 54.20 65.03 64.50 61.19 7.00 15.71 9.67 8.69 27.33 126.65
AVPP0805 54.78 86.13 63.17 33.18 5.79 14.47 9.92 4.96 95.00 396.67
AVPP0307 49.30 88.67 65.50 26.91 11.93 11.69 14.45 10.71 71.33 659.66
AVPP0506 38.77 75.47 64.50 25.31 5.58 8.85 10.14 4.77 88.00 332.80
AVPP0803 33.70 61.90 64.00 22.82 5.81 16.04 15.45 44.13 8.00 379.74
AVPP0907 41.78 88.87 69.83 42.95 5.86 16.91 6.97 2.47 46.67 263.13
AVPP0306 45.43 71.90 66.00 55.85 6.11 11.13 11.33 9.69 81.67 479.70
AVPP0804 30.60 41.40 67.50 59.85 7.36 13.04 7.83 14.00 6.33 108.69
AVPP0512 49.08 55.07 61.33 41.27 7.29 13.12 12.86 9.66 61.33 270.53
AVPP0514 38.77 67.83 67.00 19.79 5.29 16.96 14.00 12.71 68.67 582.34
AVPP0702 39.13 56.47 63.67 39.14 6.72 10.04 12.66 8.61 73.00 398.99
AVPP0103 44.20 72.43 66.33 42.05 6.54 16.12 8.99 3.54 81.67 249.99
AVPP0014 48.32 68.07 62.33 29.74 6.00 13.09 13.83 10.79 113.00 821.47
AVPP0705 46.40 83.80 63.33 16.69 6.88 3.75 8.02 3.57 151.00 349.93
AVPP0904 55.62 79.97 65.00 38.00 4.54 7.60 12.33 8.13 106.33 643.22
AVPP0513 44.43 71.80 66.00 23.16 5.62 6.02 12.60 9.64 39.33 283.38
AVPP9812 44.50 76.00 62.00 29.05 5.87 13.07 11.57 7.01 100.67 581.27
C05573 42.88 85.53 67.25 35.22 6.04 18.41 10.87 3.51 180.33 436.92
Kulai 51.50 72.17 59.00 39.96 6.44 19.32 17.23 17.68 64.00 818.10

Mean 44.23 69.53 63.89 36.37 6.58 13.12 11.58 9.58 80.18 453.55
LSD (P < 0.05) 17.35 16.47 6.56 29.06 3.99 0.066 2.69 3.19 60.61 366.29
SEM 1.16 1.45 0.45 1.96 0.23 0.020 0.27 0.72 5.53 28.57

PLH6WK: Plant height at 6 weeks; PLHH: plant height at harvest; DF: days to flowering; DI: disease incidence; CPL: chlorophyll content; Photo: photosynthesis rate; FL: fruit length; FW: fruit weight; NF: number of fruits; Y: yield; LSD: least significance difference; SEM: standard error mean.

Table 6.

The capsaicins and dihydrocapsaicin content of the thirty-six chili pepper genotype samples (mg/L).

Genotypes Capsaicin (mg/L) Dihydrocapsaicin (mg/L) Scoville Heat Units Pungency (SHUs' scale)
AVPP9703 0.00 0.00 0.00 Non-pungent
AVPP9901 205.16 84.17 36809.30 Highly pungent
AVPP9806 167.81 95.91 32731.96 Highly pungent
AVPP9813 23.28 0.00 3250.48 Moderately pungent
AVPP0002 476.03 405.55 105796.29 Very highly pungent
AVPP0012 97.87 50.52 18564.11 Moderately pungent
AVPP0102 0.00 0.00 0.00 Non-pungent
AVPP0004 13.61 0.00 1899.62 Mildly pungent
AVPP0104 439.32 445.64 104557.81 Very highly pungent
AVPP0105 120.34 78.47 24413.04 Moderately pungent
AVPP9905 175.43 241.83 47945.70 Highly pungent
AVPP9815 25.57 25.98 6090.68 Moderately pungent
AVPP0201 18.04 0.00 2519.57 Mildly pungent
AVPP0116 32.78 21.57 6669.59 Moderately pungent
AVPP9805 129.17 164.79 34015.68 Highly pungent
AVPP0109 57.15 55.10 13323.25 Moderately pungent
AVPP0305 313.05 360.08 78628.18 Highly pungent
AVPP0101 39.65 63.45 11688.78 Moderately pungent
AVPP0805 411.98 299.98 86615.90 Very highly pungent
AVPP0307 0.00 0.00 0.00 Non-pungent
AVPP0506 582.78 355.88 115887.85 Very highly pungent
AVPP0803 0.00 0.00 0.00 Non-pungent
AVPP0907 141.97 69.03 26517.41 Highly pungent
AVPP0306 107.97 84.69 23288.70 Moderately pungent
AVPP0804 18.099 0.00 2527.43 Mildly pungent
AVPP0512 0.00 0.00 0.00 Non-pungent
AVPP0514 216.78 137.03 43558.53 Highly pungent
AVPP0702 102.37 82.00 22245.67 Moderately pungent
AVPP0103 323.04 231.16 67524.10 Highly pungent
AVPP0014 48.28 13.99 8099.05 Moderately pungent
AVPP0705 1277.56 710.02 247245.28 Very highly pungent
AVPP0904 191.15 181.29 44270.75 Highly pungent
AVPP0513 70.21 51.25 15030.29 Moderately pungent
AVPP9812 23.06 12.31 4742.27 Moderately pungent
C05573 376.42 408.03 92127.13 Very highly pungent
Kulai 83.61 61.77 17665.58 Moderately pungent

Mean 175.26 133.10 37395.83
LSD (P < 0.05) 19.67 36.88 5540.40
SEM 7.22 12.31 5828.29

LSD: Least significance difference, SEM: Standard error mean.

3.3. Genotypic Variation for Heat Tolerance and Yield Characters in Chili Pepper

The significant variation among the genotypes for heat tolerance is shown in Figure 1. The figure showed that the genotypes varied with respect to heat tolerance. Most of the genotypes were found to be above the mean. Figure 2 showed variation in the genotypes with respect to yield per plant. Similarly, significant variations were observed for plant height, number of fruits, fruit length, disease incidence, and fruit weight.

Figure 1.

Figure 1

Variation among 36 chili pepper genotypes in cell membrane thermostability.

Figure 2.

Figure 2

Variation in yield per plant for 36 genotypes of Capsicum spp.

3.4. Heritability and Genetic Advance as Indices for Heat Tolerance and Morpho-Physiological Characters Selection in Chili Pepper

3.4.1. Coefficient of Variation

The extent of variability in respect of phenotypic and genotypic variances and phenotypic and genotypic coefficients of variance (GCV) for CMT and morphophysiological characters is represented in Table 6. The GCV estimate ranged from 1.73 (DF) to 75.78 (FW) over all the characters.

Moreover, high GCV and PCV were observed (>20%) in the traits for cell membrane thermostability, photosynthesis rate, disease incidence, fruit weight, and number of fruits and yield. Moderate GCV were also recorded for plant height and fruit length. The lowest were recorded for days to flowering and fruit length (<10%) (Table 7).

Table 7.

Estimate of broad sense heritability, genotypic, and phenotypic coefficients of variance, relative differences between GCV and PCV, and genetic advance for ten traits in 36 Capsicum spp.

Traits H 2 (%) σ 2 g (%) σ 2 p (%) GCV (%) PCV (%) RD GA (%)
PLH6WK 20.25 28.83 142.34 12.14 26.99 55.02 11.24
PLHH 55.06 125.32 227.59 16.1 21.7 25.81 17.11
DF 6.99 1.22 17.46 1.73 6.54 73.55 0.94
DI 17.7 68.50 387.02 22.76 54.09 57.92 19.72
CPL 2.56 −0.15 5.85 5.89 36.56 83.98 1.94
PHOTO 100 12.66 12.66 26.77 26.77 0 55
FL 66 5.30 8.03 19.88 24.47 18.76 33.27
FW 93.21 52.70 56.54 75.78 78.49 28.29 150.71
NF 54.96 1690.50 3075.60 51.28 69.17 25.86 78.31
Y 38.81 32092.80 82687.40 39.5 63.4 37.7 50.69
CMT 81.7 503.37 616.1 34.72 38.41 5.71 64.64

PLH6WK: plant height at 6 weeks; PLHH: plant height at harvest; DF: days to flowering; DI: disease incidence; CPL: chlorophyll content, PHOTO: photosynthesis rate; FL: fruit length; FW: fruit weight; NF: number of fruits; CMT: cell membrane thermostability; H 2: heritability; σ 2 g: genotypic variance; σ 2 p: phenotypic variance; Y: yield; PCV: phenotypic coefficients of variance; GCV: genotypic coefficients of variance; RD: relative difference between GCV and PCV; GA: genetic advance.

3.4.2. Heritability and Genetic Advance

Broad sense heritability values for the ten traits are presented in Table 7. Traits such as membrane thermostability, photosynthesis rate, fruit weight, and fruit length showed a relatively high heritability values (>60%). The values estimated for plant height at harvest, number of fruits and yield per plant were moderate (30–60%). Fruit length, fruit weight, number of fruits, yield, and cell membrane thermostability exhibited the highest predicted genetic advance as compared to the other traits. High heritability (>60%) together with high genetic advance (>20%) was observed for CMT, photosynthesis rate, fruit weight, and fruit length traits. However, moderate heritability with high genetic advance was observed for number of fruits and yield per plant (Table 7).

3.4.3. Correlation Coefficient

Simple phenotypic correlation coefficients for the traits studied using SAS software (version 9.1) are shown in Table 8. Yield per plant showed strong to moderately positive correlations (r = 0.23–0.56) at phenotypic level while at genotypic level correlation coefficient ranged from (0.16 to 0.72) for plant height at 6WAT and at harvest, days to flowering, fruit length, and number of fruits. However, negative correlation was observed for disease incidence with yield per plant. Similarly, cell membrane thermostability was found to correlate negatively with disease incidence. Positive phenotypic correlation between CMT and plant height and genotypic correlation between CMT and yield were also observed. Other correlation coefficients between pairs of traits that are of some interest to the breeders are shown in Table 8.

Table 8.

Coefficient of phenotypic and genotypic (bold) correlations among the investigated traits in 36 Capsicum spp.

PLHH DF DI Photo CPL FL FW NF Y CMT
PLHH 1 0.70 ** 0.49 ** 0.01 ** NA −0.03 ** −0.21 ** 0.22ns 0.19 ** 0.39ns
DF −0.11ns 1 1 ** 1 ** NA NA −1 ** −0.23 * −0.67 ** 0.04ns
DI −0.21* 0.28** 1 0.23 ** NA −0.41 ** −0.19 ** −0.22 ** −0.21 ** −0.44 **
Photo 0.01ns 0.04ns 0.08ns 1 NA 1 ** NA −0.02 ** NA −0.25 **
CPL −0.04ns −0.04ns 0.03ns −0.04ns 1 0.09 ** 0.12 ** NA NA NA
FL 0.03ns −0.27** −0.18ns 0.08ns 0.08ns 1 0.67ns −0.36 ** 0.72 ** 0.26 **
FW −0.14ns −0.08ns −0.04ns 0.12ns −0.04ns 0.60** 1 −0.59 ** 0.31 ** 0.20 **
NF 0.27** −0.27** −0.26** −0.06ns −0.07ns −0.13ns −0.40** 1 0.16 ** 0.07ns
Y 0.29** −0.38** −0.23** −0.07ns −0.07ns 0.39** 0.18ns 0.56** 1 0.35 **
CMT 0.20* 0.06ns −0.24** −0.22** −0.16ns 0.13ns 0.17ns −0.02ns 0.14ns 1

*Significant at 5%, **highly significant at 1%, PLHH: plant height at harvest; DF: days to flowering; DI: disease incidence; CPL: chlorophyll content; FL: fruit length; FW: fruit weight; NF: number of fruits; CMT: cell membrane thermostability; Photo: Photosynthesis rate; ns: not significant; NA: not available; Y: yield.

3.5. Genetic Distance-Based Analysis for Cell Membrane Thermostability and Yield

3.5.1. Cluster Analysis

The standardized data was employed to calculate the Euclidean distances among the 36 chili pepper genotypes and an UPGMA dendrogram was constructed (Figure 3). The dendrograms of the 36 chili pepper genotypes were grouped into 8 major groups based on the cell membrane thermostability and yield traits at 1.26 dissimilarity coefficients. The cutoff at this point was for the convenience of discussion. Group IV recorded the highest number with 13 genotypes followed by groups III and VI with 7 genotypes each. Group I and V recorded 4 and 2 genotypes, respectively, while groups II, VII, and VIII had 1 genotype each. Group VIII gave the highest CMT value and recorded the highest yield, while Group II gave the lowest yield and Group I gave the lowest CMT value (Table 9).

Figure 3.

Figure 3

Relationship among the 36 chilli pepper genotypes based on cell membrane thermostability and yield characters using SAHN clustering on UPGMA method.

Table 9.

Mean values of cell membrane thermostability and yield per plant characters for 8 groups revealed by cluster analysis on 36 genotypes of Capsicum spp.

Clusters Genotypes Yield CMT
Group I AVPP9703, AVPP9901, AVPP0002, AVPP0102 425.68 17.42
Group II AVPP0012 102.03 24.23
Group III AVPP9806, AVPP9815, AVPP0104, AVPP9813, AVPP0004, AVPP0109, AVPP0306 435.53 52.75
Group IV AVPP0201, AVPP0805, AVPP0803, C05573, AVPP0116, AVPP0702, AVPP0506, AVPP0513, AVPP0512, AVPP0103, AVPP9805, AVPP0907, AVPP0705 343.35 80.01
Group V AVPP0101, AVPP0804 117.67 63.53
Group VI AVPP0105, AVPP0014, AVPP0305, AVPP0904, AVPP9812, AVPP0307, AVPP0514 687.57 80.14
Group VII Kulai 818.10 49.87
Group VIII AVPP9905 1144.30 85.10

CMT: Cell membrane thermostability.

3.5.2. Principal Component Analysis

Principal component analysis was carried out on the cell membrane thermostability and yield per plant characters on the 36 genotypes. The two-dimensional graphical illustration (Figure 4) showed that most of the genotypes were dispersed at close distance while few were dispersed at great distances as reflected by the Eigen vector. The farthest genotypes from the centroid were AVPP9905, Kulai, AVPP0102, AVPP0002, AVPP9901, AVPP9703, AVPP0012, AVPP0804, and AVPP0101, while other genotypes are more or less close to the centroid. The variation percentages of the PC1 and PC2 are 62.1 and 37.9%, respectively, with PC1 showing the highest of the total variation.

Figure 4.

Figure 4

Two-dimensional graph principal component analysis showing relationship among the genotypes for cell membrane thermostability and yield.

4. Discussion

4.1. Cell Membrane Thermostability (CMT)

The membrane is the first line of defense with many heat-responsive sensors that help plants to activate defense mechanisms early in heat shock. The mean value of CMT from this investigation was 64.62% indicating in most of the genotypes that membrane integrity was not damaged by the high temperature treatment of 50°C for 20 min. This shows that most of the genotypes assessed are tolerant to heat having relative injury of <40%. Increased electrolyte leakage indicates decreased cell membrane thermostability (CMT), which has long been used as an indirect mechanism of heat-stress tolerance in several crop plant species, including tomato, potato [30], and wheat [31]. Therefore membrane leakage can be used as a means of screening vegetative plants for heat tolerance in chili pepper. This is in conformity with the works of [19] that measured CMT in 12 ornamental pepper genotypes and found most of the genotypes to be thermotolerant with a mean of 59.50%. Membrane thermostability was also measured by [4] in diverse groundnut genotypes and observed heat tolerant genotypes has low percentage of membrane leakage, with high CMT. He further reported that genotypes of diverse origin indicate different sources of tolerance to heat.

4.2. Morphophysiological Characters

The investigation revealed considerable amount of variation for the characters studied. Such wide variation indicated the scope for improving the genotypes studied for these characters with respect to heat tolerance and morphophysiological characters. High performance chili pepper genotypes, namely, AVPP9905, AVPP0105, and Kulai, in terms of growth and yield were observed in this investigation. Photosynthesis rate is the rate at which the plant can photosynthesize its own food. It measures how efficient the plant is in carbon assimilation. The variation observed in this investigation among the 36 genotypes gave room for possible selection and improvement. Similar results were observed by [32, 33] who reported significant variation in growth and yield characters of pepper genotypes. On the contrary, [34] reported significant variation among the genotypes studied for days to 50% flowering. This might be attributed to the differences in the genetic sources of the genotypes studied. In the case of degree of pungency, genotype AVPP0705 was found to record the highest capsaicin content and was the highest in pungency which was significantly (P < 0.05) higher than all the genotypes tested. Genotypes AVPP9703, AVPP0512, AVPP0307, AVPP0803, and AVPP0102 were found to record no capsaicin and therefore be non-pungent. Similar variation in capsaicin content of different peppers has been previously reported [3537]. In addition, capsaicin and dihydrocapsaicin have the same trend in contents of the capsaicinoids, and in particular capsaicin was found in higher contents than dihydrocapsaicin in all genotypes studied except C05573, AVPP9905, and AVPP9805.

4.3. Genetic Variation for Heat Tolerance and Yield Traits in Chili Pepper

The most tolerant genotypes seem to have high membrane stability (CMT > 60%) at high temperature of 50°C. Cell membrane thermostability therefore showed some potential for screening for heat tolerance in chili pepper. This is in line with the works of [38] who found large plant-to-plant variation in cell membrane thermostability measurements in Chrysanthemum cultivars. Most of the genotypes studied by [4] showed that membrane integrity was damaged by the high temperature treatment of 54°C for 15 min. On the contrary, [39] found no significant variation of CMT for ten lines of cabbage (Brassica oleracea L.). Heat tolerant genotypes having greater CMT at high temperature are said to have higher optimum and maximum temperatures for growth and development processes. This also indicates the effectiveness of cell membrane thermostability parameter as rapid and sensitive in determining heat tolerance among chili pepper genotypes. Similarly, variations were observed among the genotypes for yield indicating differences in their yield performance under the same condition. This might be due to the differences in their genetic make-up. This investigation is in harmony with the work of [32].

4.4. Heritability and Genetic Advance as Indices for Heat Tolerance and Morphophysiological Characters Selection in Chili Pepper

4.4.1. Coefficient of Variation

The extent of genetic variation in heat tolerance as well as other morphophysiological characters is better judged by the estimation of the genotypic coefficient of variation (GCV) in relation to its phenotypic coefficient of variation (PCV). A small difference between GCV and PCV was observed in plant height at harvest, fruit length, fruit weight, number of fruits, and heat tolerance characters indicating that variations among the genotypes were mostly due to genetic factors. This indicates a high significant effect of genotype on phenotypic expression with very little effect of environment. On the other hand, large differences between GCV and PCV were observed for the characters days to flowering, disease incidence, chlorophyll content, and yield per plant. This indicates the influence of the environment over these characters. High GCV observed for some traits such as CMT and yield per plant in this investigation indicates their high variability and that further selection could be used to improve the genotypes for the traits, while low GCV indicates limited improvement for the traits through selection. This is similar to the works of [40].

4.4.2. Heritability and Genetic Advance

Effective selection can be achieved only when additive effects are sufficiently higher than the environmental effect. Report from [29] showed that effectiveness of selection depends not only on heritability but also on genetic advance. High GCV together with high heritability and genetic advance provide more information than other parameters alone [41]. High heritability together with high genetic advance observed in this investigation indicates that these traits such as CMT are mainly controlled by additive type of genes. Therefore, selection may be effective for improving these traits in chili pepper. Works of [42] observed high heritability with genetic advance in several characters in chili. This investigation is in agreement with the work of [6] who observed high genetic advance accompanied with high heritability in drought tolerance in sorghum. In this study, cell membrane thermostability, fruit length, and fruit weight are found to be important characters to be taken into consideration for effective selection in pepper. Thus, selection in this population of chili pepper would prove successful once the fixed genetic component is freed from environmental influence.

4.4.3. Correlation between Traits

Relationship existing between cell membrane thermostability and disease incidence indicating the tendency of heat tolerant genotypes possesses disease resistant traits as compared to heat sensitive genotypes. As revealed from this investigation heat tolerant genotypes may be disease resistant genotypes. The likeliness of negative correlation between cell membrane thermostability and disease score as found in this study has also been reported by [43]. On the other hand, no significant association between cell membrane thermostability (heat tolerant trait) and yield per plant was observed.

4.5. Genetic Distance-Based Analysis for Cell Membrane Thermostability and Yield

Genetic divergence is one of the criteria of parent selection. Knowledge of genetic diversity among plant populations and its quantitative assessment usually helps a breeder in choosing desirable parents for breeding program as selection of parents on the basis of divergence analysis would be more effective [44].

4.5.1. Clustering Analysis

The 36 genotypes of Capsicum spp grouped into 8 clusters based on cell membrane thermostability and yield traits at distant coefficient of 1.26 indicates a level of diversity among the genotypes. Group VIII, which has only one genotype (AVPP9905), recorded the highest yield and CMT values and this proved that this genotype might have dissimilar genes as compared to the other genotypes for controlling these traits. To improve the heat tolerance of Kulai (an adaptable and susceptible genotype) that recorded the second highest yield it needs to be crossed with AVPP9905. Similarly, AVPP9905 can be crossed with AVPP0012 for high yield and heat tolerance. Similar results were obtained by [45] who studied significant variation in terms of morphological traits in distribution of chili pepper. Genetic diversity among 45 chili pepper genotypes studied by [46] observed six clusters and [16] reported eight distinct grouped in 50 accessions of chili.

4.5.2. Principal Component Analysis

The principal component analysis (PCA) yielded eigenvalues of each principal component axis of ordination of genotypes with the first axis totally accounting for the variation among the genotypes. The result of the PCA further justifies the clustering analysis. Genetically similar genotypes were grouped together. According to [7], genetically distant parents are able to exert high heterosis. Considering the variation and diversity analysis of the genotypes genotype AVPP9905 having high yield and more tolerant to heat (high CMT) from group VIII, 13 genotypes from group IV with high CMT but low yield and 7 genotypes from group VI with high CMT and Kulai with high yield and low CMT from cluster VII were found promising. Therefore, for hybridization program crosses among these genotypes for heat tolerance and yield could be effective. Similar results were observed by [46, 47].

5. Conclusion

Cell membrane thermostability is a useful parameter for thermotolerance in chili pepper. The present data indicated that most of the genotypes studied are consistently tolerant to high temperature measured based on membrane thermostability phenotyping parameter. Furthermore, these genotypes are from diverse origin indicating different sources of heat tolerance. However, the genetic parameters discussed above are function of environmental variability, so estimates may differ in other environments. High and moderate heritability and high genetic advance shown by the different characters, namely, plant height at harvest, fruit length, fruit weight and number of fruits, yield, and cell membrane thermostability determine the genetic effects of the phenotypic expression of these characters that they are fundamentally from the additive type. The prevalence of genetic variance for heat tolerance and morphophysiological traits studied can be exploited through selection as the estimate of high broad sense heritability and genetic advance allows doing so.

Considering the group distance, agronomic performance, and variability the crosses between AVPP9905 and Kulai; Kulai and AVPP0105, AVPP0014, AVPP0305, AVPP0904, AVPP9812, AVPP0307, AVPP0514; Kulai and AVPP0201, AVPP0805, AVPP0803, C05573, AVPP0116, AVPP0702, AVPP0506, AVPP0513, AVPP0512, AVPP0103, AVPP9805, AVPP0907, and AVPP0705 could be suggested for future hybridization program for heat tolerance and high yield.

Acknowledgments

The authors are grateful to Ministry of Education, Malaysia, for adequate funding of the research through the Fundamental Research Grant Scheme (FRGS/1/2012/STWN03/UPM/02/2:07-01-13-1240FR). The authors are grateful to Asian Vegetable Research and Development Centre, Taiwan, for the supply of seeds. Gratitude also goes to Yussuf Oladosu Adeniyi for his constructive criticism.

Conflict of Interests

The authors declare no conflict of interests.

Authors’ Contribution

All authors contributed equally to this work.

References

  • 1.Dahal K., Sharma M., Dhakal D., Shakya S. Evaluation of heat tolerant chilli (Capsicum annuum L.) genotypes in western terai of nepal. Journal of the Institute of Agriculture and Animal Science. 2006;27:59–64. [Google Scholar]
  • 2.Berke T., Black L. L., Talekar N. S., Wang J. F., Gniffke P., Green S. K., Wang T. C., Morris R. International Co-Operator's Guide. 2005. Suggested cultural practices for chilli pepper. [Google Scholar]
  • 3. Anim Agriculture Technology, 2013, http://animagro.blogspot.com/2011/10/chilliinMalaysia.html.
  • 4.Craufurd P. Q., Prasad P. V. V., Kakani V. G., Wheeler T. R., Nigam S. N. Heat tolerance in groundnut. Field Crops Research. 2003;80(1):63–77. doi: 10.1016/S0378-4290(02)00155-7. [DOI] [Google Scholar]
  • 5.Nechif O., Filimon R., Szilagyi L. Genetic variability, heritability and expected genetic advance as indices for yield and yield components selection in common bean (Phaseolus vulgaris L.) Scientific Papers, UASVM Bucharest, Series A. 2011;(1222-5339)
  • 6.Addissu A. G. Heritability and genetic advance in recombinant inbred lines for drought tolerance and other related traits in sorghum (sorghum bicolor) Continental Journal Agricultural Science. 2012;5:1–9. [Google Scholar]
  • 7.Falconer D. S. Introduction to Quantitative Genetics. Longman; 1981. [Google Scholar]
  • 8.Susan S. Climate Change 2007-the Physical Science Basis: Working Group I Contribution to the Fourth Assessment Report of the IPCC. Cambridge, UK: Cambridge University Press; 2007. [Google Scholar]
  • 9.Jones P. D., New M., Parker D. E., Martin S., Rigor I. G. Surface air temperature and its changes over the past 150 years. Reviews of Geophysics. 1999;37(2):173–199. doi: 10.1029/1999RG900002. [DOI] [Google Scholar]
  • 10.Suzuki N., Mittler R. Reactive oxygen species and temperature stresses: a delicate balance between signaling and destruction. Physiologia Plantarum. 2006;126(1):45–51. doi: 10.1111/j.0031-9317.2005.00582.x. [DOI] [Google Scholar]
  • 11.Wu M., Wallner S. J. Heat stress responses in cultured plant cells development and comparison of viability tests. Plant Physiology. 1983;72(3):817–820. doi: 10.1104/pp.72.3.817. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Saadalla M., Quick J., Shanahan J. Heat tolerance in winter wheat—II. membrane thermostability and field performance. Crop Science. 1990;30(6):1248–1251. [Google Scholar]
  • 13.Yeh D. M., Hsu P. Y. Heat tolerance in English ivy as measured by an electrolyte leakage technique. The Journal of Horticultural Science and Biotechnology. 2004;79(2):298–302. [Google Scholar]
  • 14.Hall A. E. Breeding for heat tolerance. Plant Breeding Reviews. 1992;10(2):129–168. [Google Scholar]
  • 15.Mahan J., McMichael B., Wanjura D. Methods for reducing the adverse effects of temperature stress on plants: a review. Environmental and Experimental Botany. 1995;35(3):251–258. doi: 10.1016/0098-8472(95)00011-6. [DOI] [Google Scholar]
  • 16.do Amarul Júnior A. T., Rodrigues R., Sudré C. P., Riva E. M., Karasawa M. Genetic divergence between “chilli” and sweet pepper accessions using multivariate techniques. Horticultura Brasileira. 2005;23(1):22–27. [Google Scholar]
  • 17.Singh R. P., Prasad P. V. V., Sunita K., Giri S. N., Reddy K. R. Influence of high temperature and breeding for heat tolerance in cotton: a review. Advances in Agronomy. 2007;93:313–385. doi: 10.1016/S0065-2113(06)93006-5. [DOI] [Google Scholar]
  • 18.Reddy K. R., Kakani V. G. Screening Capsicum species of different origins for high temperature tolerance by in vitro pollen germination and pollen tube length. Scientia Horticulturae. 2007;112(2):130–135. doi: 10.1016/j.scienta.2006.12.014. [DOI] [Google Scholar]
  • 19.Gajanayake B., Trader B. W., Reddy K. R., Harkess R. L. Screening ornamental pepper cultivars for temperature tolerance using pollen and physiological parameters. HortScience. 2011;46(6):878–884. [Google Scholar]
  • 20.Martineau J., Williams J., Specht J. Temperature tolerance in soybeans—II. Evaluation of segregating populations for membrane thermostability. Crop Science. 1979;19(1):79–81. [Google Scholar]
  • 21.Coombs J., Hind G., Leegood R., Tieszen L., Vonshak A. Analytical techniques. Techniques in Bioproductivity and Photosynthesis. 1985;2:219–228. [Google Scholar]
  • 22.Collins M. D., Wasmund L. M., Bosland P. W. Improved method for quantifying capsaicinoids in Capsicum using high-performance liquid chromatography. HortScience. 1995;30(1):137–139. [Google Scholar]
  • 23.Usman M. G., Rafii M. Y., Ismail M. R., Malek M. A., Latif M. A. Capsaicin and dihydrocapsaicin determination in chili pepper genotypes using ultra-fast liquid chromatography. Molecules. 2014;19(5):6474–6488. doi: 10.3390/molecules19056474. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.American Spice Trade Association ASTA 1985 Official Analytical Methods of the American Spice Trade Association. 3rd. Englewood Cliffs, NJ, USA: American Spice Trade Association; 1985. [Google Scholar]
  • 25.Weiss E. A. Spice Crops. New York, NY, USA: CABI Publishing International; 2002. [Google Scholar]
  • 26.Singh R. K., Chaudhary B. D. Biometrical Methods in Quantitative Genetic Analysis. Kalyani Publishers; 1979. [Google Scholar]
  • 27.Subramanian S. S., Menon M. Heterosis and inbreeding depression in rice. Madras Agricultural Journal. 1973;60:1139. [Google Scholar]
  • 28.Cherian E. Genetic variability in Capsicum chinense jacq [M.S. thesis] Kerala Agricultural University; 2000. [Google Scholar]
  • 29.Johnson H. W., Robinson H., Comstock R. Estimates of genetic and environmental variability in soybeans. Agronomy Journal. 1955;47(7):314–318. doi: 10.2134/agronj1955.00021962004700070009x. [DOI] [Google Scholar]
  • 30.Kuo C., Chen H., Sun H. Membrane thermostability and heat tolerance of vegetable leaves. Adaptation of Food Crops to Temperature and Water Stress. 1992:160–168. [Google Scholar]
  • 31.Kumar R. R., Goswami S., Sharma S. K., Gadpayle K., Kumar N., Rai G., Rai R. Protection against heat stress in wheat involves change in cell membrane stability , antioxidant enzymes, osmolyte, H2O2 and transcript of heat shock protein. International Journal of Plant Physiology and Biochemistry. 4:83–91. [Google Scholar]
  • 32.Saha S., Hossain M., Rahman M., Kuo C., Abdullah S. Effect of high temperature stress on the performance of twelve sweet pepper genotypes. Bangladesh Journal of Agricultural Research. 2010;35(3):525–534. [Google Scholar]
  • 33.Sood S., Sood R., Sagar V., Sharma K. C. Genetic variation and association analysis for fruit yield, agronomic and quality characters in bell pepper. International Journal of Vegetable Science. 2009;15(3):272–284. doi: 10.1080/19315260902875822. [DOI] [Google Scholar]
  • 34.Craufurd P. Q., Wheeler T. R. Climate change and the flowering time of annual crops. Journal of Experimental Botany. 2009;60(9):2529–2539. doi: 10.1093/jxb/erp196. [DOI] [PubMed] [Google Scholar]
  • 35.Nwokem C. O., Agbaji E. B., Kagbu J. A., Ekanem E. J. Determination of capsaicin content and pungency level of five different peppers grown in Nigeria. New York Science Journal. 2010;3(9):17–21. [Google Scholar]
  • 36.Al Othman Z. A., Ahmed Y. B. H., Habila M. A., Ghafar A. A. Determination of capsaicin and dihydrocapsaicin in Capsicum fruit samples using high performance liquid chromatography. Molecules. 2011;16(10):8919–8929. doi: 10.3390/molecules16108919. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Sanatombi K., Sharma G. J. Capsaicin content and pungency of different Capsicum spp.cultivars. Notulae Botanicae Horti Agrobotanici Cluj-Napoca. 2008;36:89–90. [Google Scholar]
  • 38.Yeh D. M., Lin H. F. Thermostability of cell membranes as a measure of heat tolerance and relationship to flowering delay in chrysanthemum. Journal of the American Society for Horticultural Science. 2003;128(5):656–660. [Google Scholar]
  • 39.Nyarko G., Alderson P. G., Craigon J., Murchie E., Sparkes D. L. Comparison of cell membrane thermostability and chlorophyll fluorescence parameters for the determination of heat tolerance in ten cabbage lines. Journal of Horticultural Science and Biotechnology. 2008;83(5):678–682. [Google Scholar]
  • 40.Manju P., Sreelathakumary I. Genetic variability, heritability and genetic advance in hot chilli (Capsicum chinense jacq.) Journal of Tropical Agriculture. 2002;40:4–6. [Google Scholar]
  • 41.Shabanimofrad M., Rafii M. Y., Megat Wahab P. E., Biabani A. R., Latif M. A. Phenotypic, genotypic and genetic divergence found in 48 newly collected Malaysian accessions of (Jatropha curcas L.) Industrial Crops and Products. 2013;42(1):543–551. doi: 10.1016/j.indcrop.2012.06.023. [DOI] [Google Scholar]
  • 42.Jabeen N., Ahmed N., Tanki M. Genetic variability in hot pepper (Capsicum annuum L.) Agricultural Science Digest. 1998;18:23–26. [Google Scholar]
  • 43.Chen Z.-Y., Brown R. L., Cleveland T. E. Evidence for an association in corn between stress tolerance and resistance to aspergillus flavus infection and aflatoxin contamination. African Journal of Biotechnology. 2004;3(12):693–699. [Google Scholar]
  • 44.Latif M. A., Yusop M. R., Rahman M. M., Talukdar M. R. B. Microsatellite and minisatellite markers based DNA fingerprinting and genetic diversity of blast and ufra resistant genotypes. Comptes Rendus Biologies. 2011;334(4):282–289. doi: 10.1016/j.crvi.2011.02.003. [DOI] [PubMed] [Google Scholar]
  • 45.Bozokalfa M. K., Eşiyok D., Turhan K. Patterns of phenotypic variation in a germplasm collection of pepper (Capsicum annuum L.) from Turkey. Spanish Journal of Agricultural Research. 2009;7(1):83–95. doi: 10.5424/sjar/2009071-401. [DOI] [Google Scholar]
  • 46.Farhad M., Hasanuzzaman M., Biswas B., Azad A., Arifuzzaman M. Reliability of yield contributing characters for improving yield potential in chilli (Capsicum annuum) International Journal of Sustainable Crop Production. 2008;3(3):30–38. [Google Scholar]
  • 47.Maqbool R., Sajjad M., Khaliq I., Rehman A., Salam K. A., Khan H. S. Morphological diversity and traits association in bread wheat (Triticum aestivum L) American-Eurasian Journal of Agricultural & Environmental Sciences. 2010;8(2):216–224. [Google Scholar]

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