Next Article in Journal
Agronomic and Economic Evaluation of Autumn Planted Sugarcane under Different Planting Patterns with Lentil Intercropping
Next Article in Special Issue
Metabolomics: A Tool for Cultivar Phenotyping and Investigation of Grain Crops
Previous Article in Journal
Remote Sensing for Precision Agriculture: Sentinel-2 Improved Features and Applications
Previous Article in Special Issue
Adaptive Grain Yield Patterns of Triticale (×Triticosecale Wittmack) Cultivars in Six Regions of Poland
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Assessing Yield and Yield Stability of Hevea Clones in the Southern and Central Regions of Malaysia

by
Muhammad Fadzli Ali
1,2,*,
Ammar Abdul Aziz
1 and
Alwyn Williams
1
1
School of Agriculture and Food Sciences, The University of Queensland, Gatton 4343, Australia
2
Department of Production Advancement, The Malaysian Rubber Board, Sungai Buloh 47000, Malaysia
*
Author to whom correspondence should be addressed.
Agronomy 2020, 10(5), 643; https://doi.org/10.3390/agronomy10050643
Submission received: 1 April 2020 / Revised: 25 April 2020 / Accepted: 27 April 2020 / Published: 1 May 2020

Abstract

:
Increased volatility in global rubber prices has led to declining Malaysian rubber production and smallholder income. Identifying rubber clones that can produce a consistently high yield in various environments is one of the potential measures to alleviate the impact of price fluctuations and improve smallholder livelihoods. In this study, we assessed rubber yields and yield stability of 37 rubber tree clones at two major production regions in Malaysia: Kota Tinggi (Southern region) and Sungai Buloh (Central region). In addition, we assessed relationships between climate data with rubber yields. Rubber yield and stability differed widely by clone, but showed relatively consistent trends across regions. Clones RRIM 2007, PB 260, and RRIM 2012 were high yielding in both regions and had high stability. Conversely, clone RRII 308 had the lowest mean yield across both regions and low stability. Mean annual yields showed a negative relationship with rising minimum temperatures, declining by ~3 g per tapping per tree (g t−1 t−1) per 1 °C rise in minimum temperature. Our findings highlight clones capable of achieving stable high yields. This information may be useful for breeders and agronomists in identifying germplasm and traits for further development. Further, this information can be used to assist clone recommendations to smallholders in these regions to mitigate the dual impacts of climate change and market volatility.

1. Introduction

Malaysia is the world’s fifth-largest rubber producer, and together with Thailand, Indonesia, Vietnam, China, and India, it contributes more than 90% of global rubber production [1,2]. Rubber (Hevea brasiliensis) is the second largest commodity produced in Malaysia after oil palm and contributes 4.7% to the national gross domestic product [3]. In addition to supporting the national income, rubber plantations also play a substantial role in providing income for smallholders. This is because smallholders dominate more than 90% of Malaysia’s rubber production [2]. The primary concern of smallholders is global rubber price fluctuations, which have trended downward in recent years [2,4]. Declining revenue drives smallholders to abandon farm management, resulting in a decline in national production [5,6]. One approach to address this issue is to ensure smallholder rubber producers are farming high yielding rubber clones with concomitant high yield stability. This would increase the consistency and productivity of rubber plantations and help secure smallholder income.
The average rubber yield produced by Malaysian smallholders is ~1400 kg ha−1 yr−1 [2], which is far below the theoretically attainable yield of 7000–12,000 kg ha−1 yr−1 [7]. This yield gap can be driven by several factors, including crop genetics [8,9], environmental conditions [10,11], and agronomic practices [12,13]. One approach to improve smallholder productivity is to develop new varieties that are well-adapted to their environment and can produce stable and high yields. Rubber research institutions commonly conduct breeding programs to identify superior clones with vigorous growth that maintain high yields during the harvesting phase, as well as explore opportunities to shorten the breeding cycle [8,14,15,16,17].
The identification of superior rubber clones is facilitated by conducting yield and stability analyses. Stability analyses have been widely applied to determine genotypic yield variability across environments [18,19,20], to identify agronomic practices that can reduce crop yield variability [21,22], to reveal patterns of crop nutrient uptake [23], to optimise the selection and shortening of rubber tree breeding cycle [24], and to determine environmental drivers of yield variability [25]. In rubber breeding programs, stability analyses have been used to identify superior clones by comparing the performance of individual clones to the average performance of a group of clones, across the harvesting period [17]. A rubber clone is considered stable if its performance across environments does not deviate significantly from the average performance of a group of standard clones [26]. The advantage of identifying superior clones through stability analysis is the reliability of those clones across environments, as they are less affected by environmental variation [27]. Several studies have utilised regression slopes to assess yield stability of Hevea clones [8,17,28,29,30,31,32]. These studies highlighted that yield variation was highly correlated with clonal genetics, girth, and environment.
Weather variability between seasons can impact rubber yields [11,33,34,35,36]. Moreover, climate change models predict increasing instability in global agricultural production [37,38,39]. In Malaysia, several studies have highlighted trends of increasing surface temperatures, sea level and extreme weather events [40,41,42]. Such changes are likely to have ongoing negative impact on Malaysian rubber production. Hence, identifying stable high-yielding rubber clones is of critical importance, both for the stability of global rubber production, and to ensure the economic viability of rubber production by smallholders. Furthermore, it is important to identify the environmental drivers of rubber yields to identify locally adapted rubber clones, as well as to understand how rubber production in different regions responds to climate change, to inform rubber breeding and selection programs, and to improve yield models. Our study builds on previous work [34], which investigated the relationship between climatic variables and a single clone (RRII 105) at a single site (Kottayam, India), and expands our understanding by investigating 37 clones across two sites.
In Malaysia, there is yet to be an evaluation of yield performance and yield stability of the newly recommended clones (2000 series) under different environmental conditions. Rubber clones have been found to respond differently to environmental variation, including climate [10,43] and soil [44,45] conditions. In this paper, we assess the yield and yield stability of 37 rubber clones at two major production regions of Peninsular Malaysia: Kota Tinggi and Sungai Buloh. Our objectives for each region were to: (1) identify high yielding clones with high stability; and (2) identify climatic factors that drive yield performance.

2. Materials and Methods

2.1. Planting Materials and Locations

Thirty-seven rubber clones from the Malaysian Rubber Board (MRB) breeding program were assessed in this study (Table S1; Supplementary material). The yield performance of these clones is currently under observation by the MRB. However, based on the preliminary results (first three years), some of the well-performing clones have already been recommended for planting in rubber farms. However, due to the limited information on the yield performance of these clones, they are recommended to only comprise between 20% and 50% of a rubber plantation, with the remainder planted with older, more well-studied clones [46]. Trees were transplanted from the nursery to the field once they developed three-whorls of leaves (approximately three to six months old), which was in June 1999. Tapping (the activity of extracting latex out of the rubber tree) began in July 2003, in line with MRB recommendations to initiate tapping upon the fifth year of planting, once the girth of the trees reaches ~45 cm at the height of 150 cm above ground-level [46].
The breeding program for the rubber clones was conducted at two MRB research stations, located at Kota Tinggi (herein referred to as the Southern region) and Sungai Buloh (herein referred to as the Central region) of Peninsular Malaysia (Figure 1). These research stations allocated clonal trial fields for MRB researchers to compare annual clonal growth and yield performance. In each region, a randomised complete block design (RCBD) was applied, which has three replicates of 30 trees per plot with 5 × 4 m spacing between rows and trees. Trees were tapped using the S/2 D/3 tapping system, which means tapping at a half spiral diameter of the trunk at three-day intervals, resulting in ~120 tapping days/year.
The yield, in the form of latex, was collected in a plastic cup attached to each tree. Yield was expressed as grams of dry rubber per tapping per tree (g t−1 t−1). This is commonly used to assess clonal yield and yield stability performance, which is the focus of this study. However, g t−1 t−1 can also be used to indicate farm performance by converting to kg ha−1 yr−1 using Equation (1):
kg · h a 1 · yea r 1   =   g · t 1 · t 1 × planting   density × tapping   days 1000
where planting density is the number of trees per hectare and tapping days is the number of tappings per year. Throughout this paper, we use g t−1 t−1 because the planting density and tapping days in MRB research trials are constant across plots. Additionally, g t−1 t−1 is not affected by tapping days, which can be influenced by rainfall intensity, price fluctuations, and labour availability. We provide the equation in case readers wish to convert our data to kg ha−1 yr−1 values. Both Southern and Central regions have similar annual temperatures, while the Southern region is marked by greater mean annual rainfall (Table 1). The Southern region has soil class III, while the Central region has soil class IV. Within Malaysia, soils have been split into five classes based on their suitability for growing rubber [47]; this is based on seven soil parameters including depth, slope, texture, rock percentage, drainage, pH, and nutrient level. Soil class I is considered most suitable for growing rubber, while class V is the least suitable.

2.2. Data Collection

Data for rubber yield and weather were compiled from July 2003 to June 2010 (Southern region; seven years) and July 2003 to June 2007 (Central region; four years). The MRB recorded yield on a monthly basis as an average of the 30 trees per clone per plot (Department of Crop Protection and Improvement). Daily climate data for the periods mentioned were obtained from the NASA Langley Research Center (LaRC) POWER Project (funded through the NASA Earth Science/Applied Science Program). The NASA POWER Project data is designed to provide agroclimatological data for input into crop models. NASA POWER Project climate data has been found to compare favourably with local weather station data [48,49] and several studies have reported close agreement between crop yields estimated from NASA POWER climate data and observed yields in the field [49,50]. Climate data for the relevant time periods was collected for both locations and consisted of minimum, maximum and mean temperatures, and rainfall and relative humidity (RH). Vapour pressure deficit (VPD) was subsequently calculated using Equation (2) [51]:
VPD = V P sat × ( 1 RH 100 )
where VPsat is the saturated vapour pressure deficit. Daily VPsat values were calculated based on daily air temperature values using Equation (3) [51], where T is the daily air temperature:
V P sat = 610.78 × 10 ( 7.5 T T + 237.3 )
Annual climate data were calculated as within-year averages (July to June) based on daily data. While local weather station data would be preferable to the NASA POWER data, the nearest weather stations were determined to be not representative of the study sites as they are located >80 km from the site and have different altitudes and annual rainfall.

2.3. Yield Stability Analysis

Several metrics have been developed to assess crop yield stability, including regression coefficients [52], coefficient of variation (CV) [53], and Taylor’s Power Law Residuals (POLAR) [54]. The appropriate metric to use has been shown to be dependent on the structure of the data [54]. For this reason, we calculated all three metrics to determine the most appropriate one for our dataset.
The regression slope approach was conducted through the development of linear mixed effects models (LMEs) using the ‘nlme’ package of R software [55]. LME are an extension of simple linear models that allow both fixed and random effects and are particularly useful when there is nonindependence in the data, such as arises from a hierarchical structure [56]. For example, when there are multiple levels in a structure, such as yield performance of multiple clones in the same region, the variability in the outcome can be interpreted as being either within-clones or between-clones. We compared annual population rubber yields (defined as Environmental Index, EI) for each of the two locations over 2003–2010 (Southern region) and 2003–2007 (Central region) in relation to variation in individual clonal annual yields over the same period. Throughout our LME analyses, the most parsimonious model was selected based on the Akaike Information Criteron (AIC) and validated by plotting model residuals.
Each model contained a clone-level random intercept and slope structure, and the EI was fitted as the fixed effect. The equation was represented by the following model structure in R: clonal mean rubber yield ~ EI, random = ~ EI | clone. Individual clonal minimum yield potential (MYP) values were calculated from LME predictions of rubber yield at the minimum EI for each location. MYP is the minimum yield a clone produced under the observed worst environmental conditions (for each site this was determined to be the year with the lowest yield). High MYP is important because it indicates clones that provide the greatest relative yields and therefore income under poor environmental conditions. The regression slope for each clone was obtained as the best linear unbiased predictors (BLUPs) from the LME. The value of the coefficient defines yield stability, where <1 is stable, 1 is the average population stability (i.e., matches 1:1 with the EI), and >1 is less stable and thus more sensitive to environmental fluctuations [57]. The CV for each clone within a location was calculated as the quotient of rubber yield standard deviation over mean rubber yield.
POLAR was calculated as the residuals of a linear relationship of log variance and log yield. POLAR is a recently developed yield stability metric based on Taylor’s Power Law and has been presented as an alternative to the regression slope and CV approaches, which are considered to have several drawbacks [54]. For the regression slope approach, if variances scale with environmental means, the confidence interval for yields of individual varieties becomes broader, and the regression slope of residuals from the environmental slope increases as the environmental mean increases. On the other hand, the CV can either increase or decrease with an increasing yield based on the slope values (b > 2 for the former, and b < 2 for the latter), or constant if b = 2. These arguments impose that slope and CV may be strongly correlated with yield, and therefore may not be reliable and independent yield stability metrics. However, the drawbacks of POLAR include lower visibility of relationships to yield when comparing treatments or genotypes with similar means and requires many measurements of yield to observe the relationships [54].
We compared the suitability of these three stability metrics for assessing rubber clone yield stability by conducting a Pearson correlation analysis of each metric with yield. The stability metric with the lowest correlation with yield was chosen as the most suitable one. We then plotted our chosen yield stability metric against clonal mean yield and superimposed a quadrant centered on the median values of clonal mean yield and our yield stability metric (Figure 2). Clones that are high yielding with high yield stability are located in the bottom right quadrant (Figure 2). Hence, use of these clones would help ensure smallholder productivity is both greater and more stable.

2.4. Rubber Yields and Climatic Data

In this analysis, we excluded yield data from the first year of harvesting as it is typically associated with lower yields [46] that can confound interpretation of the impact of climate on yields. This process reduced our data sets to six years (Southern region) and three years (Central region); because of the limited data set for the Central region, only data from the Southern region was analysed. The relationship between rubber yields and climate variables was analysed using LME. The average annual value for each weather variable, covering maximum and minimum temperatures, precipitation, humidity and VPD, was used in relation to yield.

3. Results and Discussion

3.1. Mean Yields and Yield Stability

Clonal annual yield averages (EI and individual clones) were ranked from the ‘worst’ to ‘best’ performing years to quantify clonal yield stability [52] (Figure 3). Figure 3A (Southern region) and Figure 3B (Central region) show the performance of each clone against the EI compared to the population mean. The overall average yields were 51 g t−1 t−1 and 54 g t−1 t−1 for the Southern and Central regions, respectively. The results show that mean yields at both locations were similar, but that rubber clones varied widely in terms of productivity and stability. Interestingly, the top three clones in the Central region outperformed all clones in the Southern region, despite the Central region having a lower soil quality rating.
MYP and mean yields were positively correlated (Southern region: r = 0.99, p < 0.001; Central region: r = 0.99, p < 0.001; Figure S1A,B; Supplementary material), demonstrating that clones that performed better on average were also able to maintain higher yields under the worst environmental conditions observed during the study. Consequently, it may be preferable to plant clones with high MYP to secure a minimum level of productivity under suboptimal growing conditions. In both regions, LME regression slopes showed a strong positive relationship with mean yield (Figure 4A–C (Southern region), Figure 4D–F (Central region)), demonstrating that LME regression slopes are not independent of mean yield. This violates the compatibility of this metric to measure yield stability for our dataset [54].
In contrast, CV and POLAR showed no correlation with mean yields (for CV, Southern region: r = −0.22, p = 0.19; Central region: r = −0.09, p = 0.6; and for POLAR, Southern region: r = 0.14, p = 0.4; Central region: r = 0.14, p = 0.4; Figure 4). This demonstrates that CV and POLAR are independent of mean yield, indicating they are robust yield stability metrics for our data [54]. The more stable clones have both a lower CV and POLAR, which means there is less variation of yield across the harvesting period of that clone. In our subsequent analyses to identify stable and high yielding clones, we have chosen to present our results using POLAR due to its better presentation of independence from mean yield compared with CV and LME slopes (Figure 4).
The categorisation of each clone into yield stability quadrants is shown in Figure 5A (Southern region) and Figure 5B (Central region). In this paper, we only present the results of the quadrants for mean yields due to the high correlation identified between the mean yield and MYP. The clonal mean yield and stability ranking (derived from the bottom-right quadrants) for the Southern and Central region is presented in Table S2; Supplementary material.
Clones that have higher yields (>50 g t−1 t−1) and stability than the population median in both the Southern and Central regions include RRIM 2007 and PB 260 (Figure 5). This finding is comparable with earlier research, which investigated yield performance based on three harvesting years in a large-scale clone trial [46]; however, the research did not consider the impact of different regions on the clonal yield performance. For RRIM 2007, our findings are consistent with the [46] trial, where it produced the highest yield (an average of 74 g t−1 t−1) compared to other clones. RRIM 2007 was reported to possess excellent secondary traits, including vigour at opening tapping panel, disease resistance, and yield potential [46]. In contrast, PB 260 was low yielding (27 g t−1 t−1) in the [46] trial. PB 260 was found to have poor resistance toward tapping panel dryness and virgin bark at opening tapping panel, and moderate resistance toward disease and wind damage, which may have contributed to the low yield [46]. Our results indicate that not only do both these clones produce high yields in the Central and Southern regions, their yields were also stable across the harvesting period. Additional high performing clones (stable and high yielding) in the Southern region were RRIM 928, RRIM 2001 and RRIM 2009, which yielded higher than the population median yields (>50 g t−1 t−1). These results are similar to what was reported from the large-scale clone trial [46]. These clones were reported to have excellent vigour and virgin bark at opening tapping panel, and resistance toward tapping panel dryness and wind damage [46]. Additional high performing clones identified in this study in the Central region were PB 372 and PB 374 (mean yields for both are ~73 g t−1 t−1 and ~81 g t−1 t−1, respectively); the yield performance of these two clones has not been evaluated in previous studies.
In both regions, clones RRII 308, RRII 109, and RRIM 2014 showed low mean yields (17 g t−1 t−1, 22 g t−1 t−1, and 40 g t−1 t−1 at Southern; and 22 g t−1 t−1, 24 g t−1 t−1, and 39 g t−1 t−1 at Central) and low stability, and hence are not recommended for smallholders in these regions. This result is consistent with the findings presented by [58], where significantly higher CV (lower stability) and lower mean yields were observed in clone RRII 308 compared to clone RRIM 600 (Malaysian clone). However, [58] also revealed that despite RRII 308 having low mean yields, it produced competitive yields during winter months, indicating the importance of accounting for seasonal variation in clone yield performance. In the large-scale clone trial conducted by [46], RRIM 2014 had low mean yield (39 g t−1 t−1) [46], which is consistent with our finding. RRII 109, on the other hand, has not been studied previously in these regions, but based on this study appears unsuitable for planting. These findings highlight the role of cultivar origin in impacting clonal yield performance (e.g., clones from India generally performed poorly in the two regions in Malaysia in this study) and thus the importance of local clone breeding to ensure good yield performance.

3.2. Rubber Yields and Climate

Climatic factors have significant impact on rubber yield. For example, temperature and relative humidity influence tree stomata regulation, which affects latex flow [34,59,60], and rainfall intensity affects smallholders tapping activity [61]. In our study, the fixed effects are represented by the weather variables of minimum, maximum and mean temperatures, rainfall, relative humidity and VPD, while the fitted random effect was clone. The best-supported model indicates minimum temperature as the only significant variable and is negatively related to clonal mean yield (Figure 6).
Although three of the 37 clones showed increases in yields as minimum annual temperatures increased, the other 34 clones showed a negative relationship (r = −0.97, p < 0.001). Across all clones, an increase of 1 °C minimum temperature reduced yield by ~3 g t−1 t−1 (Figure 6). We found that the highest yield occurred at 23 °C and decreased as the minimum temperature increased, with the lowest yield at 26 °C. This finding is consistent with the literature, where rising minimum temperatures have been found to have a negative relationship with rubber yield [11,33]. While daytime temperatures of 27–33 °C are optimal for photosynthesis [62], temperatures above 22 °C are unfavourable for latex flow due to the increased evapotranspiration rates [63]. Further, decreased yield with higher minimum temperature suggests that higher night-time respiration reduces moisture availability within the tree, resulting in lower yield [34,64]. This finding highlights the potential impact of climate change on rubber yield. Current climate models indicate a continuous increase in minimum temperatures [65,66,67], which can lead to greater declines in latex yields due to an increase in tree respiration [68]. In addition to moisture loss, increasing respiration causes reductions in tree carbon-use efficiency, i.e., it increases losses of photosynthetically fixed carbon as CO2 at the expense of conversion to proteins, carbohydrates and other compounds that comprise latex [61]. However, our analysis is based on NASA POWER data, which has a 0.5° latitude, longitude grid cell spatial resolution. Consequently, while our analysis points to a significant negative influence of rising minimum temperatures on rubber tree productivity, local long-term climate data is needed to confirm this trend.
Previous studies have found an inverse relationship between latex yields and VPD through changes to turgor pressure in tree laticifers [7,69,70]. High VPD also causes tree trunk shrinkage [71]. Thus, the absence of a relationship between yield and VPD in our study (r = −0.002, p = 0.7) was surprising. A previous study [71] reported that tree trunk shrinkage was only affected when VPD is >1 kPa. In our dataset, the average VPD value was 0.25 kPa, which may explain why no relationship was observed.

4. Conclusions

In this study, yield stability analysis of 37 Hevea clones in two different environmental conditions represented by the Southern and Central regions in Malaysia was conducted. We used three yield stability metrics to assess the clonal yield stability; we found that POLAR was the most suitable metric due to its lower correlation with mean yield and better presentation of independence from mean yield compared with CV and LME slopes. Clone RRIM 2007 was identified as the most stable and highest yielding with the greatest MYP in both the Southern and Central regions. The mean yields of this clone at the Southern and Central regions were 78 g t−1 t−1 and 75 g t−1 t−1, respectively. These yields are substantially higher than the current mean yields of each region (27 g t−1 t−1 at Southern and 28 g t−1 t−1 at Central [2]). Thus, greater planting of RRIM 2007 in these regions may help improve smallholder productivity and income. The importance of this is underscored by the increased volatility in global rubber prices, which increases risk for smallholders. By planting the recommended clones, smallholders are more likely to ensure high yield during poor environmental conditions and maintain higher yield across the harvesting period, thereby minimising the impact of price fluctuations on their revenues. This quadrant-based analysis can also be used in other regions to identify high yielding and stable clones.
We also found that an increase of 1 °C minimum temperature was associated with a reduction in latex yields of ~3 g t−1 t−1. Globally, minimum temperatures are projected to continue to increase, based on general circulation models. This further highlights the importance of identifying clones that can perform well under poor environmental conditions and facilitating policy on planting those identified clones to minimise the impact of climate change on rubber production.

Supplementary Materials

The following are available online at https://www.mdpi.com/2073-4395/10/5/643/s1, Figure S1: Relationship between minimum yield potential (g t−1 t−1) and mean yields (g t−1 t−1), Table S1: Rubber tree clones examined in this study, Table S2: Clonal mean yield and stability ranking derived from the optimal quadrant for the Southern and Central region.

Author Contributions

Conceptualization, M.F.A., A.A.A. and A.W.; methodology, A.W.; software, A.W.; validation, M.F.A., A.A.A. and A.W.; formal analysis, M.F.A. and A.W.; investigation, M.F.A.; resources, M.F.A.; data curation, M.F.A. and A.W.; writing—original draft preparation, M.F.A.; writing—review and editing, M.F.A., A.A.A. and A.W.; visualization, M.F.A., A.A.A. and A.W.; supervision, A.A.A. and A.W.; project administration, A.A.A. and A.W. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Acknowledgments

The authors wish to thank the Malaysian Rubber Board for providing the yield data, and to Puan Siti Hawa Sulong, Fauzi Mohd Som, and Encik Zarawi Ab Ghani for supporting this research.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Fox, J.; Castella, J.C. Expansion of rubber (Hevea brasiliensis) in Mainland Southeast Asia: What are the prospects for smallholders? J. Peasant Stud. 2013, 40, 155–170. [Google Scholar] [CrossRef]
  2. MRB. Pocket Book 2020; Malaysian Rubber Board: Kuala Lumpur, Malaysia, 2020. [Google Scholar]
  3. Sharib, S.; Halog, A. Enhancing value chains by applying industrial symbiosis concept to the Rubber City in Kedah, Malaysia. J. Clean. Prod. 2017, 141, 1095–1108. [Google Scholar] [CrossRef]
  4. Goh, H.H.; Tan, K.L.; Khor, C.Y.; Ng, S.L. Volatility and market risk of rubber price in Malaysia: Pre- and Post-global financial crisis. J. Quant. Econ. 2016, 14, 323–344. [Google Scholar] [CrossRef]
  5. Wee, S.M.W.J.; Singaravelloo, K. Income Targets and Poverty of Rubber Smallholders. J. Malays. Inst. Plan. 2018, 16, 381–396. [Google Scholar]
  6. Purcell, T.D. The Factors Affecting the Long Run Supply of Rubber from Sarawak, East Malaysia, 1900–1990—An Historical and Econometric Analyis. Master’s Thesis, The University of Queensland, Brisbane, Australia, 8 November 1993. [Google Scholar]
  7. Paardekooper, E.C. Exploitation of the Rubber Tree. Rubber 1989, 5, 349–414. [Google Scholar]
  8. Gonçalves, P.D.S.; Silva, M.D.A.; Gouvêa, L.R.L.; Scaloppi Junior, E.J. Genetic variability for girth growth and rubber yield in Hevea brasiliensis. Sci. Agric. 2006, 63, 246–254. [Google Scholar] [CrossRef] [Green Version]
  9. Vinod, K.K.; Suryakumar, M.; Chandrasekhar, T.R.; Nazeer, M.A. Temporal stability of growth and yield among Hevea genotypes introduced to a non-traditional rubber growing region of peninsular India. Ann. For. Res. 2010, 53, 107–115. [Google Scholar]
  10. Das, G.; Reju, M.J.; Mondal, G.C.; Singh, R.P.; Thapliyal, A.P.; Chaudhuri, D. Adaptation of Hevea brasiliensis clones in three widely different cold prone areas of northeastern India. Indian J. Plant Physiol. 2013, 18, 231–239. [Google Scholar] [CrossRef]
  11. Priyadarshan, P.M. Contributions of weather variables for specific adaptation of rubber tree (Hevea brasiliensis Muell.-Arg) clones. Genet. Mol. Biol. 2003, 26, 435–440. [Google Scholar] [CrossRef]
  12. Njukeng, J.N.; Muenyi, P.M.; Ngane, B.K.; Ehabe, E.E. Ethephon stimulation and yield response of some Hevea clones in the humid forests of South West Cameroon. Int. J. Agron. 2011, 2011, 1–5. [Google Scholar] [CrossRef] [Green Version]
  13. Soumahin, E.F.; Obouayeba, S.; Anno, P.A. Low tapping frequency with hormonal stimulation on Hevea brasiliensis clone PB 217 reduces tapping manpower requirement. J. Anim. Plant Sci. 2009, 2, 109–117. [Google Scholar]
  14. Gonçalves, P.D.S.; Luiz Teixeira de Moraes, M.; de Almeida Silva, M.; Regina Lima Gouvêa, L.; Tosoni da Eira Aguiar, A.; Brito da Costa, R. Prediction of Hevea progeny performance in the presence of genotype-environment interaction. Braz. Arch. Biol. Technol. 2009, 52, 25–33. [Google Scholar] [CrossRef]
  15. Priyadarshan, P.M.; Dey, S.K.; Nazeer, M.A.; Varghese, Y.A.; Kang, M.S. Adaptability analysis of rubber (Hevea Brasiliensis Muell.-Arg.) clones via GGE biplot. J. Rubber Res. 2008, 11, 237–244. [Google Scholar]
  16. Silva, G.A.P.; Gouvêa, L.R.L.; Verardi, C.K.; Oliveira, A.L.B.; de Gonçalves, P.D.S. Annual growth increment and stability of rubber yield in the tapping phase in rubber tree clones: Implications for early selection. Ind. Crop. Prod. 2014, 52, 801–808. [Google Scholar] [CrossRef]
  17. Thanh, T.; Tuy, L.M.; Lam, L. Van. Genotype × environment interaction of Hevea clones in traditional and non-traditional rubber growing regions of Vietnam. J. Plant Interact. 2016, 11, 20–29. [Google Scholar] [CrossRef] [Green Version]
  18. De Vita, P.; Mastrangelo, A.M.; Matteu, L.; Mazzucotelli, E.; Virzì, N.; Palumbo, M.; Storto, M.; Lo Rizza, F.; Cattivelli, L. Genetic improvement effects on yield stability in durum wheat genotypes grown in Italy. Field Crop. Res. 2010, 119, 68–77. [Google Scholar] [CrossRef]
  19. Piepho, H.P. Methods for comparing the yield stability of cropping systems—A review. J. Agron. Crop Sci. 1998, 180, 193–213. [Google Scholar] [CrossRef]
  20. Zhe, Y.; Lauer, J.G.; Borges, R.; de Leon, N. Effects of genotype × environment interaction on agronomic traits in soybean. Crop Sci. 2010, 50, 696–702. [Google Scholar]
  21. Berzsenyi, Z.; Gyorffy, B.; Lap, D. Effect of Crop Rotation and Fertilisation on Maize and Wheat Yields and Yield Stability. Eur. J. Agron. 2000, 13, 225–244. [Google Scholar] [CrossRef]
  22. Macholdt, J.; Honermeier, B. Yield stability in winter wheat production: A survey on German farmers’ and advisors’ views. Agronomy 2017, 7, 45. [Google Scholar] [CrossRef] [Green Version]
  23. Basso, B.; Shuai, G.; Zhang, J.; Robertson, G.P. Yield stability analysis reveals sources of large-scale nitrogen loss from the US Midwest. Sci. Rep. 2019, 9, 1–9. [Google Scholar] [CrossRef] [PubMed]
  24. Chandrasekhar, T.R.; Marattukalam, J.G.; Mercykutty, V.C.; Priyadarshan, P.M. Age of yield stabilization and its implications for optimising selection and shortening breeding cycle in rubber (Hevea brasiliensis Muell. Arg.). Euphytica 2007, 156, 67–75. [Google Scholar] [CrossRef]
  25. Williams, A.; Hunter, M.C.; Kammerer, M.; Kane, D.A.; Jordan, R.; Mortensen, D.A.; Smith, R.G.; Snapp, S.; Davis, A.S. Soil Water Holding Capacity Mitigates Downside Risk and Volatility in US Rainfed Maize: Time to Invest in Soil Organic Matter? PLoS ONE 2016, 11, e0160974. [Google Scholar] [CrossRef] [PubMed]
  26. Gonçalves, P.D.S.; Bortoletto, N.; Martins, A.L.M.; Costa, R.B.; da Gallo, P.B. Genotype-environment interaction and phenotypic stability for girth growth and rubber yield of Hevea clones in São Paulo State, Brazil. Genet. Mol. Biol. 2003, 26, 441–448. [Google Scholar] [CrossRef]
  27. Koo, Y.B.; Yeo, J.K.; Woo, K.S.; Kim, T.S. Selection of superior clones by stability analysis of growth performance in Populus davidiana Dode at age 12. Silvae Genet. 2007, 56, 93–101. [Google Scholar] [CrossRef] [Green Version]
  28. Gonçalves, P.D.S.; Martins, A.L.M.; Bortoletto, N.; Saes, L.A. Selection and genetic gains for juvenile traits in progenies of Hevea in São Paulo State, Brazil. Genet. Mol. Biol. 2004, 27, 207–214. [Google Scholar] [CrossRef]
  29. Gonçalves, P.D.S.; Júnior, E.J.S.; Martins, M.A.; Moreno, R.M.B.; Branco, R.B.F.; Gonçalves, E.C.P. Assessment of growth and yield performance of rubber tree clones of the IAC 500 series. Pesqui. Agropecu. Bras. 2011, 46, 1643–1649. [Google Scholar] [CrossRef] [Green Version]
  30. Gouvêa, L.R.L.; Silva, G.A.P.; Verardi, C.K.; de Oliveira, A.L.B.; Gonçalves, E.C.P.; Scaloppi-Junior, E.J.; de Moraes, M.L.T.; Gonçalves, P.D.S. Rubber tree early selection for yield stability in time and among locations. Euphytica 2013, 191, 365–373. [Google Scholar] [CrossRef]
  31. Silva, G.A.P.; Gouvêa, L.R.L.; Verardi, C.K.; Resende, M.D.V.; Scaloppi Junior, E.J.; Gonçalves, P.S. Genetic parameters and correlation in early measurement cycles in rubber trees. Euphytica 2013, 189, 343–350. [Google Scholar] [CrossRef]
  32. Souza, A.M.D.; Gouvêa, L.R.L.; de Oliveira, A.L.B.; Silva, G.A.P.; Gonçalves, P.D.S. Estimates of genetic parameters for the rubber yield and secondary traits in rubber tree. Ind. Crop. Prod. 2017, 98, 19–24. [Google Scholar] [CrossRef]
  33. Golbon, R.; Ogutu, J.O.; Cotter, M.; Sauerborn, J. Rubber yield prediction by meteorological conditions using mixed models and multi-model inference techniques. Int. J. Biometeorol. 2015, 59, 1747–1759. [Google Scholar] [CrossRef] [PubMed]
  34. Rao, P.S.; Saraswathyamma, C.K.; Sethuraj, M.R. Studies on the relationship between yield and meteorological parameters of para rubber tree (Hevea brasiliensis). Agric. For. Meteorol. 1998, 90, 235–245. [Google Scholar] [CrossRef]
  35. Yang, X.; Blagodatsky, S.; Marohn, C.; Liu, H.; Golbon, R.; Xu, J.; Cadisch, G. Climbing the mountain fast but smart: Modelling rubber tree growth and latex yield under climate change. For. Ecol. Manag. 2019, 439, 55–69. [Google Scholar] [CrossRef]
  36. Yu, H.; Hammond, J.; Ling, S.; Zhou, S.; Edward, P.; Xu, J. Greater diurnal temperature difference, an overlooked but important climatic driver of rubber yield. Ind. Crop. Prod. 2014, 62, 14–21. [Google Scholar] [CrossRef]
  37. Isik, M.; Devadoss, S. An analysis of the impact of climate change on crop yields and yield variability. Appl. Econ. 2006, 38, 835–844. [Google Scholar] [CrossRef]
  38. Rosenzweig, C.; Elliott, J.; Deryng, D.; Ruane, A.C.; Müller, C.; Arneth, A.; Boote, K.J.; Folberth, C.; Glotter, M.; Khabarov, N.; et al. Assessing agricultural risks of climate change in the 21st century in a global gridded crop model intercomparison. Proc. Natl. Acad. Sci. USA 2014, 111, 3268–3273. [Google Scholar] [CrossRef] [Green Version]
  39. Webber, H.; Gaiser, T.; Ewert, F. What role can crop models play in supporting climate change adaptation decisions to enhance food security in Sub-Saharan Africa? Agric. Syst. 2014, 127, 161–177. [Google Scholar] [CrossRef]
  40. Suhaila, J. Trend analysis and change point detection of annual and seasonal temperature series in Peninsular Malaysia. Meteorol. Atmos. Phys. 2018, 130, 565–581. [Google Scholar] [CrossRef]
  41. Tang, K.H.D. Science of the total environment climate change in Malaysia: Trends, contributors, impacts, mitigation and adaptations. Sci. Total Environ. 2019, 650, 1858–1871. [Google Scholar] [CrossRef]
  42. Wong, C.; Yusop, Z.; Ismail, T. Trend of daily rainfall and temperature in Peninsular Malaysia based on gridded data set. Int. J. 2018, 14, 65–72. [Google Scholar] [CrossRef]
  43. Withanage, S.P.; Attanayake, G.; Karunasekara, K.A. Adaptability of recently recommended rubber clones for agro-climatic variability of Sri Lanka. J. Rubber Res. Inst. Sri Lanka 2005, 87, 1–6. [Google Scholar] [CrossRef] [Green Version]
  44. Daud, W.N. Rubber Plantation: Soil Management & Nutritional Requirement; Universiti Putra Malaysia Press: Serdang, Malaysia, 2013. [Google Scholar]
  45. Mokhatar, S.J.; Daud, N.W.; Ishak, C.F. Response of Hevea Brasiliensis (RRIM 2001) planted on an Oxisol to different rates of fertilizer application. Malays. J. Soil Sci. 2012, 16, 57–69. [Google Scholar]
  46. MRB. Rubber Plantation and Processing Technologies; Malaysian Rubber Board: Kuala Lumpur, Malaysia, 2009. [Google Scholar]
  47. Yew, F.K.; Chan, H.Y. Soil suitability classification systems for Hevea brasiliensis cultivation. J. Nat. Rubber Res. 1992, 7, 290–302. [Google Scholar]
  48. White, J.W.; Hoogenboom, G.; Wilkens, P.W.; Stackhouse, P.W.; Hoel, J.M. Evaluation of satellite-based, modeled-derived daily solar radiation data for the continental United States. Agron. J. 2011, 103, 1242–1251. [Google Scholar] [CrossRef] [Green Version]
  49. Monteiro, L.A.; Sentelhas, P.C.; Pedra, G.U. Assessment of NASA/POWER satellite-based weather system for Brazilian conditions and its impact on sugarcane yield simulation. Int. J. Climatol. 2018, 38, 1560–1570. [Google Scholar] [CrossRef]
  50. Van Wart, J.; Kersebaum, K.C.; Peng, S.; Milner, M.; Cassman, K.G. Estimating crop yield potential at regional to national scales. Field Crop. Res. 2013, 143, 34–43. [Google Scholar] [CrossRef] [Green Version]
  51. Kattel, D.B.; Yao, T.; Yang, W.; Gao, Y.; Tian, L. Comparison of temperature lapse rates from the northern to the southern slopes of the Himalayas. Int. J. Climatol. 2015, 35, 4431–4443. [Google Scholar] [CrossRef]
  52. Hildebrand, P.E.; Russell, J.T. Adaptability Analysis: A Method for the Design, Analysis and Interpretation of On-Farm Research-Extension; Iowa State University Press: Ames, IA, USA, 1996. [Google Scholar]
  53. Smith, R.G.; Menalled, F.D.; Robertson, G.P. Temporal yield variability under conventional and alternative management systems. Agron. J. 2007, 99, 1629–1634. [Google Scholar] [CrossRef] [Green Version]
  54. Döring, T.F.; Knapp, S.; Cohen, J.E. Taylor’s power law and the stability of crop yields. Field Crop. Res. 2015, 183, 294–302. [Google Scholar] [CrossRef]
  55. Team, R.C. A Language and Environment for Statistical Computing 2016; R Foundation for Statistical Computing: Vienna, Austria, 2016. [Google Scholar]
  56. Galecki, A.; Burzykowski, T. Linear Mixed-Effects Models Using R; Springer: Berlin/Heidelberg, Germany, 2013. [Google Scholar]
  57. Finlay, K.W.; Wilkinson, G.N. The analysis of adaptation in a plant breeding. Aust. J. Agric. Resour. 1963, 14, 742–754. [Google Scholar] [CrossRef] [Green Version]
  58. Kumar, S.; Das, G.; Mydin, K.K. Performance of some Hevea clones under the cold prone climate of Sub-Himalayan West Bengal. Rubber Sci. 2015, 28, 37–44. [Google Scholar]
  59. Carr, M.K.V. The water relations of rubber (hevea brasiliensis): A review. Exp. Agric. 2012, 48, 176–193. [Google Scholar] [CrossRef]
  60. Priyadarshan, P.M. Biology of Hevea Rubber; CABI: Preston, UK, 2011. [Google Scholar]
  61. Priyadarshan, P.M. Biology of Hevea Rubber; Springer International Publishing AG: Cham, Switzerland, 2017. [Google Scholar]
  62. Zongdao, H.; Xueqin, Z. Rubber cultivation in China. In Proceedings of the Rubber Research Institute of Malaysia Planters’ Conference, Kuala Lumpur, Malaysia, 17–19 October 1983; pp. 31–43. [Google Scholar]
  63. Shuochang, A.; Yagang, G. Exploration of the high yield physiological regulation of Hevea brasiliensis in Xishuangbanna. In Proceedings of the IRRDB Symposium on Physiology and Exploitation of Hevea Brasiliensis, Kunming, China, 6–7 October 1990; pp. 83–92. [Google Scholar]
  64. Jiang, A. Climate and natural production of rubber (Hevea brasiliensis) in Xishuangbanna, southern part of Yunnan province, China. Int. J. Biometeorol. 1988, 32, 280–282. [Google Scholar] [CrossRef]
  65. Emmanuel, L.A.; Batablinlè, L.; Célestin, M.; Hodabalo, K. Future extremes temperature: Trends and changes assessment over the Mono River Basin, Togo (West Africa). J. Water Resour. Prot. 2019, 11, 82–98. [Google Scholar] [CrossRef] [Green Version]
  66. Fallah-Ghalhari, G.; Shakeri, F.; Dadashi-Roudbari, A. Impacts of climate changes on the maximum and minimum temperature in Iran. Theor. Appl. Climatol. 2019, 138, 1539–1562. [Google Scholar] [CrossRef]
  67. Li, L.; Yao, N.; Li, Y.; Liu, D.L.; Wang, B.; Ayantobo, O.O. Future projections of extreme temperature events in different sub-regions of China. Atmos. Res. 2019, 217, 150–164. [Google Scholar] [CrossRef]
  68. Zhou, Y.F. Rubber Cultivation in Yunnan; Yunnan University Press: Kunming, China, 2008; p. 176. [Google Scholar]
  69. Devakumar, A.S.; Rao, G.G.; Rajagopal, R.; Rao, P.S.; George, M.J.; Vijayakumar, K.R.; Sethuraj, M.R. Studies on soil-plant-atmosphere system in Hevea. II. Seasonal effects on water relations and yield. Indian J. Nat. Rubber Res. 1988, 1, 45–60. [Google Scholar]
  70. Rao, G.G.; Rao, P.S.; Rajagopal, R.; Devakumar, A.S.; Vijayakumar, K.R.; Sethuraj, M.R. Influence of soil, plant and meteorological factors on water relations and yield in Hevea brasiliensis. Int. J. Biometeorol. 1990, 34, 175–180. [Google Scholar] [CrossRef]
  71. Junjittakarn, J.; Limpinuntana, V.; Do, F.C.; Pannengpetch, K.; Isarangkool Na Ayutthaya, S.; Rocheteau, A.; Cochard, H. Vapour pressure deficit affects diurnal girth fluctuation of rubber trees (Hevea brasiliensis). Aust. J. Crop Sci. 2011, 5, 1622–1630. [Google Scholar]
Figure 1. Location of the breeding programs in Peninsular Malaysia (Kota Tinggi: Southern and Sungai Buloh: Central regions).
Figure 1. Location of the breeding programs in Peninsular Malaysia (Kota Tinggi: Southern and Sungai Buloh: Central regions).
Agronomy 10 00643 g001
Figure 2. An example of a quadrant plot of yield stability metric against mean yield (g t−1 t−1).
Figure 2. An example of a quadrant plot of yield stability metric against mean yield (g t−1 t−1).
Agronomy 10 00643 g002
Figure 3. Linear mixed effects models of clone-level yields across all years against location-specific annual mean yield (environmental index). Thick black lines show location mean fixed effect. Grey lines show individual clone relationships (best linear unbiased predictors (BLUPs)) as estimated from the model random effects structure. (A) Southern (for the fixed effect: y = 0.11x + 4.59, conditional r2 = 0.77); (B) Central (for the fixed effect: y = 0.16x + 7.53, conditional r2 = 0.85).
Figure 3. Linear mixed effects models of clone-level yields across all years against location-specific annual mean yield (environmental index). Thick black lines show location mean fixed effect. Grey lines show individual clone relationships (best linear unbiased predictors (BLUPs)) as estimated from the model random effects structure. (A) Southern (for the fixed effect: y = 0.11x + 4.59, conditional r2 = 0.77); (B) Central (for the fixed effect: y = 0.16x + 7.53, conditional r2 = 0.85).
Agronomy 10 00643 g003
Figure 4. Relationship between stability parameters with mean yield (AC) Southern; (DF) Central.
Figure 4. Relationship between stability parameters with mean yield (AC) Southern; (DF) Central.
Agronomy 10 00643 g004
Figure 5. Clonal position in quadrant stability plot for (A) Southern and (B) Central regions. Dashed lines show the median values of mean yield (x) and POLAR (y).
Figure 5. Clonal position in quadrant stability plot for (A) Southern and (B) Central regions. Dashed lines show the median values of mean yield (x) and POLAR (y).
Agronomy 10 00643 g005
Figure 6. Linear mixed effects models of clone-level yields against annual minimum temperature. The thick black line shows the mean fixed effect. Grey lines show individual clone relationships (best linear unbiased predictors (BLUPs)) as estimated from the model random effects structure. For the fixed effect: y = −3.24x + 130.54, conditional r2 = 0.82.
Figure 6. Linear mixed effects models of clone-level yields against annual minimum temperature. The thick black line shows the mean fixed effect. Grey lines show individual clone relationships (best linear unbiased predictors (BLUPs)) as estimated from the model random effects structure. For the fixed effect: y = −3.24x + 130.54, conditional r2 = 0.82.
Agronomy 10 00643 g006
Table 1. Environmental conditions in the Southern region (2003 to 2010) and the Central region (2003 to 2007).
Table 1. Environmental conditions in the Southern region (2003 to 2010) and the Central region (2003 to 2007).
VariableKota Tinggi Research Station (Southern Region)Sungai Buloh Research Station (Central Region)
Latitude1.7294° N3.2093° N
Longitude103.8992° E101.5613° E
Elevation (m)1431
Annual mean temperature (°C)27.027.5
Annual mean rainfall (mm)27552478
Soil series and classBungor, IIIHolyrood, IV

Share and Cite

MDPI and ACS Style

Ali, M.F.; Abdul Aziz, A.; Williams, A. Assessing Yield and Yield Stability of Hevea Clones in the Southern and Central Regions of Malaysia. Agronomy 2020, 10, 643. https://doi.org/10.3390/agronomy10050643

AMA Style

Ali MF, Abdul Aziz A, Williams A. Assessing Yield and Yield Stability of Hevea Clones in the Southern and Central Regions of Malaysia. Agronomy. 2020; 10(5):643. https://doi.org/10.3390/agronomy10050643

Chicago/Turabian Style

Ali, Muhammad Fadzli, Ammar Abdul Aziz, and Alwyn Williams. 2020. "Assessing Yield and Yield Stability of Hevea Clones in the Southern and Central Regions of Malaysia" Agronomy 10, no. 5: 643. https://doi.org/10.3390/agronomy10050643

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