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Assessment of the Potential Impacts of Wheat Plant Traits across Environments by Combining Crop Modeling and Global Sensitivity Analysis

Assessment of the Potential Impacts of Wheat Plant Traits across Environments by Combining Crop Modeling and Global Sensitivity Analysis

  • Pierre Casadebaig, 
  • Bangyou Zheng, 
  • Scott Chapman, 
  • Neil Huth, 
  • Robert Faivre, 
  • Karine Chenu
PLOS
x

Abstract

A crop can be viewed as a complex system with outputs (e.g. yield) that are affected by inputs of genetic, physiology, pedo-climatic and management information. Application of numerical methods for model exploration assist in evaluating the major most influential inputs, providing the simulation model is a credible description of the biological system. A sensitivity analysis was used to assess the simulated impact on yield of a suite of traits involved in major processes of crop growth and development, and to evaluate how the simulated value of such traits varies across environments and in relation to other traits (which can be interpreted as a virtual change in genetic background). The study focused on wheat in Australia, with an emphasis on adaptation to low rainfall conditions. A large set of traits (90) was evaluated in a wide target population of environments (4 sites × 125 years), management practices (3 sowing dates × 3 nitrogen fertilization levels) and CO2 (2 levels). The Morris sensitivity analysis method was used to sample the parameter space and reduce computational requirements, while maintaining a realistic representation of the targeted trait × environment × management landscape (∼ 82 million individual simulations in total). The patterns of parameter × environment × management interactions were investigated for the most influential parameters, considering a potential genetic range of +/- 20% compared to a reference cultivar. Main (i.e. linear) and interaction (i.e. non-linear and interaction) sensitivity indices calculated for most of APSIM-Wheat parameters allowed the identification of 42 parameters substantially impacting yield in most target environments. Among these, a subset of parameters related to phenology, resource acquisition, resource use efficiency and biomass allocation were identified as potential candidates for crop (and model) improvement.

Introduction

Progress in plant breeding is limited by the ability to predict plant phenotype based on its genotype, especially for complex traits such as yield. Suitably constructed process-based models provide a mean to reduce this gap in particular by dissecting the complexity of the genotype-environment interactions and by simulating expected impacts in various environmental conditions [13], including consideration of future climates [4, 5].

From a modeling point of view, crops are complex systems arising from interactions among genetic determinants, physiological processes, pedo-climatic factors and management practices. The combination of these elements, which are either chosen (cultivar and management) or given (soil and climate) in any sown crop, generates greatly variable stress patterns [6, 7] and results in high genotype (G) × environment (E) × management (M) interactions. A number of such interactions has been reported in the literature [8, 9], and sources of yield variation, especially in rainfed systems, commonly arise primarily from the genotype × environment (G×E) interactions, rather than the genotype (G), i.e. G×E > G as observed for field pea in Canada [10], sunflower in Argentina [11], sorghum in Australia [12], wheat in north-east Australia [13] and globally [14] and maize in Midwestern US states [15, 16] Modeling approaches have been developed to better understand G×E×M interactions and attempt to take advantage of genetic and environmental resources more efficiently. For example, Hammer et al. [17] show that the multi-year risk of crop failure for farms within a given sorghum region can be reduced by the adoption of better combinations of GxM (“local G” and “local M”) compared to use of the combination of “global G” and “global M” that would be adopted if using the entire sorghum production area.

Process-based crop models are useful tools to integrate scientific knowledge and simulate varietal or management impacts on productivity in the target population of environments (TPE), i.e. the set of environments to which newly bred varieties need to be adapted [18, 19]. Hence, the predictive capability of crop models is used to explore the complex G×E×M landscape and assists breeding programs to take advantage of genetic and environmental resources more efficiently [2, 20, 21]. While such models are based on mathematical equations translating biological processes in relation to crop growth and development, their parameters can be controlled to mimic effects of genotypic variability and explore the G×E×M landscape using virtual genotypes [22, 23]. Numerical exploration of crop models for the target population of environments thus allows exploration of the entire G×E×M landscape, assuming that the crop simulation model gives a credible description of the biological system.

To be relevant, exploration of the G×E×M landscape has to be applied to environments and management practices related to targeted production systems. A recent study characterized the drought environment of rainfed wheat for the Australian target population of environments [7], an interesting target given that Australia is the fourth wheat exporter worldwide and that Australian wheat crops have to adapt to a high variability (spatial and inter-annual) in drought patterns, which strongly impedes crop breeding [9, 13, 24] The Australian wheatbelt extends ca. 13 million ha (Australian Bureau of Statistics, 2013) and has soils ranging from shallow sandy to deep clay soils and include temperate, Mediterranean and subtropical climates [25, 26]. Chenu et al. [7] undertook a simulation-based study (60 sites × 5 initial soil moisture × 5 sowing dates) to capture the variability in environmental and management conditions of this TPE. To study genotypic variation in such a TPE raises computational challenges if variations in multiple plant traits with high granularity (resolution) are desired, i.e. requiring the simulation of many levels of small increment for each of the factors explored.

The APSIM (www.apsim.info) Wheat model [2729] is used to simulate crop performance as a function of plant traits, pedo-climatic variability and management practices. This model has been extensively used and tested across Australia [6, 27, 28, 30]. Numerical experiments with crop models allow exploration of large G×E×M landscape. However, sampling the G×E×M landscape using a factorial design with as few as six levels for each parameter of the APSIM-Wheat model in the Australian TPE considered in this study would require to perform 9.72 × 1073 simulations. Such an approach would require absurdly high computing resource and could be considered as partly wasteful given that it considers all parameters including those of minimal importance. An alternative is to apply a numerical method designed to more efficiently explore complex landscapes. For instance, global sensitivity analysis allows investigation of how the uncertainty in the output of a model can be apportioned to different sources of uncertainty in the model input [31, 32].

Few computational studies have used sensitivity analysis to address cropping problems, e.g assessing the impact of phenology and management on sugarcane yield in various environments [33], the influence of geometrical and topological traits on light interception efficiency of apple trees [34] and the impact of physiological traits on wheat grain yield and protein concentration in Europe [35]. Recently, Zhao at al. [36] performed a sensitivity analysis on the APSIM-Wheat model with a focus on a narrow set of cultivar-specific traits (10 parameters) with the aim to improve an incoming calibration step.

The aims of this paper were (i) to assess the impact of a suite of physiological traits on yield for Australian rain-fed wheat crops and (ii) to evaluate how the value of such traits varies across environments and in relation to other traits. A large set of traits (103) were evaluated in APSIM-Wheat for a wide population of environments related to four representative locations [7, 24] and 125 years of historical records of weather data (Fig 1). In addition to this representative set of 500 environment conditions, simulations were performed for three sowing dates, three levels of nitrogen fertilization and two levels of CO2 (i.e. 9000 conditions in total) to assess the effects of management and CO2 factors. We used a global sensitivity analysis to determine the effects of all traits on yield for all the conditions studied (i.e. each site × year × management combination). Traits found to have substantial and frequent impacts on yield were further studied through variance analysis to investigate the influence of environmental-factors and their impact on integrated traits such as plant leaf area, biomass production, and grain size and number.

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Fig 1. Framework of crop model simulation and the sensitivity approach used to assess the potential impact of plant traits.

A global sensitivity analysis was applied on the APSIM-Wheat crop model to identify potential candidate traits for yield improvement in a large population of environments. This workflow presents how the “genetic diversity” was considered, sampled and screened in silico. In summary, 90 independent APSIM-Wheat parameters considered as “component traits”, associated with the main physiological processes that are modeled, were selected to reflect a potential genetic variability. Each of the 90 component traits was assumed to vary in a ± 20% range around the value for the reference cultivar Hartog and the Morris method [37, 38] was used to sample the total parameter space (90 traits, 6 levels, 100 reps; i.e. 9100 “genotypes”). Simulations for those genotypes were performed with APSIM-Wheat (Version 7.5). The impact of the 90 component traits were considered for 8 output variables (“integrated traits”, which result from the complexity of the dynamic modeling of development and growth). The impact on crop yield allowed to screen component traits for influential traits (n = 42) in the target population of environments while a study on trait × environment interactions was used to explore their variability across environments.

https://doi.org/10.1371/journal.pone.0146385.g001

Material and methods

Overview

A global sensitivity analysis was applied on the APSIM-Wheat crop model to identify potential candidate traits for yield improvement in a large population of environments. Fig 1 describes this workflow, showing how the “genetic diversity” was considered, sampled and screened in silico. In summary, from 516 parameters of the APSIM-Wheat model (with a broad-sense definition of parameter which included e.g. physical constants, optional parameters used for other crops and parameters repeated for different stages), 90 independent parameters that could be considered as “component traits” were selected to reflect a potential genetic variability. Each of the 90 component traits was assumed to vary in a ± 20% range around the value for the reference cultivar Hartog. The number of considered traits prevented the use of a factorial design, and so the Morris method [37, 38] was used to sample the total parameter space (90 traits, 6 levels, 100 reps; i.e. 9100 “genotypes”). Simulations for those genotypes were performed with APSIM-Wheat (Version 7.5) for (1) 4 locations and 125 years (from 1889 to 2013) to test the impact of component traits in the TPE (Table 1) and (2) for 3 sowing dates (i.e. early, TPE-level and late), 3 levels of nitrogen (i.e. low, TPE-level and high fertilization) and 2 levels of CO2 (380 and 555 ppm to represent CO2 level in 2010 and 2050) to test trait impact in other environmental conditions related to farmer management practices and future climates. The impact of the 90 component traits were considered for 8 output variables (“integrated traits”, Table 2) related to phenology (flowering and maturity dates), leaf development (Leaf Area Index at flowering), biomass production (at maturity), and grains (grain number, size, protein and yield). Overall 42 component traits were identified as “influential” (i.e. main average impact on yield greater than 20 kg ha-1) and considered as potential candidates to improve yield in the TPE. They were analyzed in more detail with a variance analysis. Several interesting traits related to phenology, resource acquisition, resource use efficiency and biomass allocation were studied in more detail as their impact could be related to specific environmental factors. A more complete description of the workflow and analysis is given below.

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Table 1. Characteristics of the locations, soils and management representing the target population of environments.

Plant available water capacity (PAWC) is indicated for each soil, as well at the level of initial soil water used in the simulations (median of plant available water at sowing which was estimated from [7]). Applied nitrogen dose are indicated by “a/b/c”: respectively, the fertilization applied at sowing (a), at the stage “end of tillering” (b) and at the stage “mid-stem elongation” (c). Annual and seasonal (1-May to 1-Nov) climatic data were considered for 1889-2013.

https://doi.org/10.1371/journal.pone.0146385.t001

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Table 2. Description of integrated traits (APSIM-Wheat output variables) and environmental indices included in the analysis.

Environment indices were computed for the sowing-harvest period, for all considered environments. Water-deficit index correspond to the simulated water supply-demand ratio and relates to the degree to which the water available to the roots matches the plant water demand [7]. Nitrogen stress index relates to the level of nitrogen stress on photosynthesis. Stress indices are expressed as scalars so that values range from 0 (low stress) to 1 (high stress).

https://doi.org/10.1371/journal.pone.0146385.t002

Simulations and sensitivity analysis

A global sensitivity analysis was performed on parameters of the crop model APSIM-Wheat version 7.5 [28, 29] to assess their impact on yield in the Australian wheatbelt (Figs 12). Five main steps were followed: (1) listing the input APSIM-Wheat parameters (input factors) to be included in the analysis, (2) setting the variation range for each factor, (3) sampling the parameter space with the Morris method, (4) simulating the virtual experiment with APSIM-Wheat and (5) computing the sensitivity indices to assess the impact of each factor singly (main effect) or in combination (interaction).

1. Defining input factors.

As for most crop models, APSIM-Wheat has parameters (S1 Table) that specify quantitative effect of processes related directly or indirectly to crop growth and development [2729, 39]. Those parameters are typically either single values or arrays of paired vectors (S1 Table and S1 Fig), in which case one vector relates to the piloting a state variable (x; e.g. stage values) and the second one corresponds to the considered trait (y; e.g. values of root biomass partitioning for the different key stages considered). Each defined value, whether it is a single-value parameter or a point in an array can be considered as a parameter; in which case, APSIM-Wheat has 516 parameters (v. 7.5, as documented in Zheng et al. [29]). As all numerical coefficients in APSIM are completely external to the code, these “parameters” actually included a lot of constants and coefficients that would never be changed. Not all parameters were considered when assessing the impact of plant traits on crop performance as (1) four parameters representing soil physics and general physical constants (e.g. ammonium diffusion rate) were not considered, (2) 22 parameters deliberately set to have no impact on wheat crops (e.g. multiplicative scalars which are set to 1.0 by default in the released version of APSIM-Wheat) were not considered and (3) values in vectors (parameter arrays) were considered as dependent parameters, counting one parameter for the whole “function”.

This process greatly reduced the number of parameters to 103 (62 single values and 41 functions), yet there was no information loss on the system description. In addition, some parameters were grouped [38] to avoid aberrant situations and computational errors (e.g new min thresholds being greater than new max thresholds). In total, 20 parameters (annotated with * in S1 Table) were grouped into 7 “meta-parameters” that govern their variation (e.g. nitrogen demand, leaf expansion processes). Overall, 90 parameters (p = 103 − 20 + 7 = 90) were considered in the sensitivity analysis, with all the crop processes from APSIM-Wheat being tested (i.e. no process was removed from the analysis).

2. Setting the variation range.

The range of parameter values is biologically constrained by the genetic diversity existing in wheat. However, most crop models have typically been designed to only simulate major differences among cultivars (e.g. phenology), as their primary aim has been to address crop management problems. As a result, crop models such as APSIM-Wheat only have a few parameters that are by default considered as cultivar-dependent, while all the other parameters are assumed to be constant for the species. Given the lack of knowledge related to the range of the genetic variability existing for most of the model parameters, a fixed range of 40% variation for all parameters was tested in the sensibility analysis. Where possible, equal variation around the nominal value (± 20%) was considered, but for hard-bounded parameters (e.g scalars comprised between 0 and 1) the 40% variation was considered below (or above) the nominal value. Nominal values were considered for the reference cultivar Hartog and scaled using two consecutive rules: (1) direct scaling of the single value, or of all the y vector for function parameters (e.g. proportion of biomass partitioned to the roots at different stages) and (2) scaling only one single point in the x or y vector when this improved the biological meaning (e.g. threshold of leaf-expansion sensitivity to water deficit). S1 Fig illustrates the shape and variation range for function parameters studied in this sensitivity analysis.

3. Sampling the parameter space.

We used the Morris method [37] as implemented by Campagnolo et al. [38] to sample the parameter space and compute sensitivity indices. The method consists in a discretization of the input space for each factor (n = 6 levels), then performing a given number of one-at-a-time (OAT) design (r = 100) on the 90 parameters. The OAT designs were randomly chosen in the input space, and the variation direction was also random but their dispersion in the input space was maximized [38]. The repetition 100 times of these steps allowed the estimation of elementary effects for each input factor [37]. The implementation in the sensitivity R package used the space-filling optimization of the design [38]. Parameter design was normalized to account for the different magnitudes in input factors (parameters expressed in different units).

Considering the total number of input factors and the sampling conditions, the total size of parameter design was 90 + 1 × 100 = 9100, where each sample (i.e. set of parameter values) can be interpreted as a virtual genotype (i.e. 9100 in total). The numerical sampling of the parameter space can be viewed as an exploration of virtual genotype materials where there is no restriction in the combination of traits considered (i.e. no genetic linkage or epistasis).

4. Design of experiments for crop simulations.

The previous parameter design (i.e. the 9100 parameter combinations) was used with the APSIM-Wheat crop model to simulate 9100 virtual genotypes. APSIM-Wheat simulations were first done for the target population of environments (TPE, i.e. control conditions, Table 1) defined by 4 sites (Emerald, Narrabri, Yanco and Merredin; Fig 2, Table 1) and 125 years (1889-2013) of climatic data (4 × 125 = 500 environments). Crop management in these simulations (Table 1) was chosen to mimic local farming practices [7]. Additional simulations were performed for 3 sowing dates 21/04; 15/05; 07/06), 3 nitrogen fertilization levels (low: 50% of TPE-level, TPE-level and high fertilization: TPE-level plus 50 kg.ha-1) and 2 CO2 levels (TPE-level of 380 ppm and 555 ppm to represent CO2 level in 2010 and 2050) to explore the impact of parameters in contrasting N and CO2 conditions.

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Fig 2. Map of the studied sites and climatic variability in aridity index.

The map shows potential evapotranspiration over precipitation ratio (1 / aridity index, data from Zomer et al. [41]), points correspond to locations sampled in the target population of environments.

https://doi.org/10.1371/journal.pone.0146385.g002

Nitrogen fertilization rules followed an APSIM decision model: at sowing, nitrogen was applied as nitrate in Merredin and as urea in the rest of the wheatbelt. In Yanco, fertilisation at “end of tillering” stage only occurred if cumulative rainfall since sowing was greater than 100 mm, and fertilisation at “mid-stem elongation” stage only occurred if plant available water was greater than 60% of the PAWC. At Merredin, fertilisation at “mid-stem elongation” only occurred if plant available water was greater than 60 mm.

Overall, 9000 (3 × 3 × 2 × 500 = 9000) environmental conditions were tested, and 81.9 million of crops (9100 × 9000) were simulated on the CSIRO distributed computing cluster which can sustain a peak throughput of approximately 8000 simultaneous processes [40]. Parameter impacts were tested on eight output variables from APSIM (Table 2): number of days from sowing to flowering and from sowing to maturity, leaf area index (LAI), biomass production, the number, size and protein content of grains and yield.

The baseline simulations were performed with the reference cultivar Hartog to estimate environmental indices (Table 2) and crop performance in each environment. In addition, the growing environments were characterized in terms of drought environment types, as described in Chenu et al. [7].

5. Computation of sensitivity indices.

Sensitivity indices were computed as statistics of elementary effect, i.e effect of the factor for each repetition [37, 38]. In this approach, the main effect (noted in Iooss et al. [42]) is a measure of the influence of the i-th input on the output, and is calculated as the mean of the absolute value of the elementary effects. The larger is, the more the input contributes to the dispersion of the output. The interaction effect (σi in Iooss et al. [42]), is a measure of non-linear and/or interaction effects of the i-th input. σi is computed as the standard deviation of the elementary effects. An input with a large σi can be considered as having non-linear effects or being involved in an interaction with at least another input. We also computed a standardized sensitivity index to be able to compare indices across different output variables and growing conditions. In this case, for each growing environment, the model output variables were standardized () before computing elementary effects and sensitivity indices.

Clustering parameters according to their impact

All of the considered parameters were subdivided into three groups according to the mean value of their main effect in the target population of environments (i.e. mean of across environments): (1) null impact group, in which parameters had no impact on crop yield in any environments (2) low impact group, in which the parameters had an average lower or equal to 0.02 t ha-1 and (3) impactful group, in which parameters had an average main effect on yield that was greater than 0.02 t ha-1. A hierarchical clustering based on Ward distance was applied to the matrix of impactful parameters and the eight output variables (averaged across environments) to group these parameters and identify those with similar patterns of effect on output variables.

Analysis of trait × environment interactions and computation of environment indices

For plant traits corresponding to influential parameters, we conducted a variance analysis to assess the effects of environmental factors on the variability of impact. Hence, for each trait, a linear model (Eq 1.) was fitted with environment-related factors considered as categorical fixed effects and with no interaction as Y = αsite + βsowing + γCO2 + δnitrogen + ϵ with Y, vector of main effects for one trait in the 9000 environments; α, β, γ, δ are the additive main effects of the levels in factor CO2, site, sowing and nitrogen, respectively (Eq 1.). The effect of each environmental factor (e) on trait impact was estimated by the proportion of total sum of square (η2) as SSe/(TSS). Note that both the effect of “uncontrollable” environmental factors (i.e. climate) and the interactions among factors were pooled in the residuals.

Finally, we considered the response to the environment of a small subset of candidate traits and defined several environmental stress indices (Table 2) to further illustrate the ecophysiological basis of trait × environment interactions. Using the ASPIM Wheat model, daily computed indices related to water and nitrogen stresses were averaged for the duration of the crop cycle. In the model, water-stress is computed as a function of the soil water extractable by roots (water supply) and potential crop transpiration (water demand) [7]. The nitrogen-stress determined the limiting nitrogen level affecting leaf photosynthesis [29]. In this study, both indices were set to range from 0 (no-stress) to 1 (extreme stress) to allow comparison between stress indices.

Software

All data processing, statistical analysis and graphics were performed with R 3.1.0 [43] with additional R packages dplyr (data processing [44]), sensitivity (sensitivity analysis, version 1.10.1 [45]) and ggplot2 (visualization [46]).

Results

A target population of environments with contrasting environmental conditions

Four sites were chosen to capture part of the variability in soil types and rainfall patterns that are experienced across the dryland wheatbelt (Table 1; Fig 1). Simulated yield for 1889-2013 reflected these differences in environments, with median yield ranging from 1.72 t ha-1 in Emerald to 4.10 t ha-1 at Narrabri (Fig 3). High inter-annual variability was also simulated and reflected the broad range of water deficits and temperature events that Australian wheat experience across seasons [5, 7].

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Fig 3. Heatmap of yield response to climate and management practices in all growing environments studied.

Simulated yield for cv. Hartog is presented for each sites (Emerald, Merredin, Narrabri, Yanco), CO2 levels (380 and 555 ppm), sowing dates (21 April, 15 May, 7 June), fertilization (x-axis, potential mineral nitrogen applied before decision model, in kg ha-1) and climatic years (y-axis) i.e 9000 growing environments in total.

https://doi.org/10.1371/journal.pone.0146385.g003

About a half of the studied traits had little or no impact on yield in the target population of environments (TPE)

A global sensitivity analysis was performed to get a general picture of the effect of APSIM-Wheat parameters on yield response in the TPE. While the results from the sensitivity analysis strongly depend on the ranges of variation for the input traits, such ranges are scarcely available for all the considered traits despite numerous studies and reviews giving informative indications of partial genetic ranges for some traits [4750]. To perform a broad screen of parameters, the sensitivity analysis was done with variations of ± 20% from the reference value (Hartog cultivar) of each parameter (S1 Table), except for some function parameters for which variations were adapted to increase the biological likelihood of the results (see S1 Fig). Another analysis was conducted with variation of ± 50% to test a broader range of variation, but this led to a high proportion of crop failure, due in particular to excessive senescence (data not shown).

About half of the studied traits (48/90) were not or only weakly impacting yield (average effect of less than 20 kg ha-1) in the TPE (Fig 4). Among those traits, 21 had no impact on yield or any other of the studied output variables (i.e. flowering, maturity, LAI, biomass, grain number, size and protein) in any environments. Two options could explain such null impacts: (1) the parameter corresponding to the trait simply did not have any role in the model algorithm for wheat (some parameters are only used for other crops in the APSIM framework) or (2) the traits were influential only in agricultural conditions other than tested here (e.g the sum of temperature until emergence failure, tt_emerg_limit).

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Fig 4. Screening for influential traits in the TPE (control conditions).

Traits were ranked by increasing mean main sensitivity index and were grouped into three groups (panels): null impact, low impact and impactful group. Note that all impacts are positive, as given by the sensitivity analysis method. A description of traits is presented in S1 Table. Concerning sensitivity indexes, the main effect (circle) is an estimation of the linear influence of the considered trait on grain yield, while the interaction effect (cross) is an estimation of non-linear and/or interaction effect(s) of the trait. The horizontal dashed line corresponds to the 20 kg ha-1 threshold above which traits are considered as impactful.

https://doi.org/10.1371/journal.pone.0146385.g004

The other 27 traits showed a weak mean impact on yield (< = 20 kg ha-1) in the TPE, often because the conditions required to induce a substantial impact are rarely encountered. This group included traits that may have been considered as important a priori, such as potential leaf area (y_leaf_size) or maximum temperature for thermal-time accumulation (x_temp).

Traits with a mean impact on yield of > 20 kg ha-1 were considered in more detail (42 traits; Fig 4). Overall, 29 traits had a mean impact between 20 and 25 kg ha-1, eight traits had an impact between 25 and 50 kg ha-1, and only five traits had a mean impact greater than 50 kg ha-1. The five most influential traits in terms of both mean and interaction effects ( and σi) in the tested conditions were: the water extractability by roots (ll_modifier), the thermal time required to reach floral initiation (tt_end_of_juvenile), the photoperiod sensitivity (photop_sens), the radiation use efficiency (y_rue), and the radiation extinction coefficient (y_extinct_coef).

Among the 42 influential traits, only a few showed a linear impact on yield, i.e. their main effect was greater than their interaction effect, e.g. the fraction of biomass partitioned to the spike rachis (y_frac_pod), the water extractability by roots (ll_modifier), the wheat coefficient for transpiration efficiency (transp_eff_cf) and the temperature effect on grain demand (x_temp_grain_fill). Most of the influential traits had a ratio of interaction:main effect between 1 and 1.8, denoting either a large non-linear effect or an effect largely influenced by other traits. Traits such as senescence-related traits and grain potential biomass (max_grain_size) had higher ratio (> 1.8).

Several traits had a strong impact on physiological processes related to phenology, biomass and grain production

To better understand the effects of plant traits in the TPE, the 42 influential component traits were clustered based on their main effect on eight integrated traits related to phenology, leaf area, and nitrogen and carbon accumulation and partitioning (Fig 5). Component traits were mainly clustered in three groups (dashed line in Fig 5): lesser influential traits, traits that strongly impacted all outputs, and traits that strongly impacted a subset of integrated traits.

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Fig 5. Overview of APSIM-Wheat sensitivity to trait modification.

The heatmap shows the impact (positive in the Morris method) of selected component traits (model inputs, x-axis) modification on integrated traits (model outputs, y-axis). Component traits (top dendrogram) and integrated traits (right dendrogram) were ordered with hierarchical clustering based on the similarities among impacts. Trait impact was standardized to be comparable across integrated traits (model output variables).

https://doi.org/10.1371/journal.pone.0146385.g005

Overall, crop phenology (flowering and maturity time) was mostly affected by six component traits (thermal time from emergence to floral initiation, from floral initiation to flowering and to a lesser extent from flowering to the beginning of grain filling; photoperiod sensitivity and two leaf senescence traits), while the remaining traits had little to no impact. Traits affecting grain-filling (x_temp_grain_n_filling, x_temp_grainfill, potential_grain_filling_rate) were clustered together, and had a high impact on grain size, grain protein and yield. On the other hand, about another 10 traits were found to substantially impact leaf area, biomass and grain production. As may be expected, the water extractability (ll_modifier), which affects the maximum amount of soil water that can be extracted, impacted traits such as LAI at flowering, biomass at maturity, grain number and yield. The trait grains_per_gram_stem which relates to the potential of the crop to set grains based on its carbon status (proportional to stem weight at flowering), affected grain number but had a relatively little impact on yield given trade-offs on grain size in these largely water-limited environments.

Globally, the impact pathway of traits on physiological processes reflected the sub-component of the crop model where parameters were involved.

Impacts of influential traits were strongly dependent on environmental and management conditions

The variability of trait impacts arose from high trait × environment interactions (Fig 6), i.e. the modification of a trait did not result in the same change in output trait depending on the growing conditions. Main yield impacts of individual component traits ranged from 0.02 t ha-1 (screening threshold) to 2.87 t ha-1 (potential radiation use efficiency, y_rue, under high nitrogen conditions).

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Fig 6. Yield sensitivity to a variation of selected influential trait.

Trait main impacts were calculated from a sensitivity analysis and are presented for different nitrogen treatments (A), sowing dates (B) and sites (C) and in the TPE (control conditions) unless mentioned (i.e. high/low nitrogen, early/late sowing).

https://doi.org/10.1371/journal.pone.0146385.g006

Most traits had a larger yield impact when management practices and climatic conditions were “non-limiting”, e.g. high fertilization, high soil water holding capacity (Yanco, Narrabri) and early sowing (i.e. long cropping season). By contrast, response traits (e.g. x_temp_grain_fill, transp_eff_cf) impacted yield in more extensive conditions (e.g. low nitrogen). For instance, water extractability by roots (ll_modifier) had more impact for late-sown than for early-sown crops, as such crops are more prone to drought.

Identification of influential traits with low dependence to climate uncertainty

The variance of trait impacts on yield across the 9000 studied environments was partitioned for each studied traits into four controllable environmental factors (site, sowing date, nitrogen fertilization and CO2 level) and one uncertainty-related factor (residuals) that aggregated the factor year, the interaction among “controllable” factors and the residuals (Fig 7). Despite the coarseness of the approach and the fact that trait main impacts were only considered as absolute value (no distinction between negative and positive impact on yield), traits with both a strong mean impact and an impact variability that mainly depends on “controllable” factors would potentially be easier for consideration for breeding.

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Fig 7. Variance components of trait main impact for major environmental factors.

For each influential trait, the proportion of variance explained by environmental factors (site, nitrogen fertilization, sowing date and CO2 level) was calculated in an ANOVA on simulated yield for crops in the 9000 studied growing conditions. Traits were clustered in groups based on the proportion of explained variance by environmental factors (horizontal panels). Cluster identified corresponded to traits mainly impacted by site and sowing date (first panel), nitrogen fertilization (second panel), CO2 (third panel) and traits having a high residual component (fourth panel).

https://doi.org/10.1371/journal.pone.0146385.g007

Traits were a posteriori clustered in four groups (horizontal panels in Fig 7), which can be described as: (1) site/sowing impact, which may be related to water or temperature driven processes, (2) nitrogen impact, (3) CO2 impact and (4) high residuals (uncertainty). Traits in the site/sowing, nitrogen and CO2 groups displayed both high and relatively stable main impact on yield. The nitrogen-impact group included all studied traits related to grain filling, indicating that modifications of such traits could reliably impact yield providing adequate nitrogen fertilization. On the other hand, the site/sowing-driven group included traits such as the potential radiation use efficiency (y_rue), the light extinction coefficient (y_extinct_coef) and the potential leaf surface area (y_sla), which may be linked to the available water resources or thermal regime (e.g. short/long crop cycle). Traits in the high residuals group were influential but not stable, meaning that a modification of such traits did not yield the same return depending on years and/or due to interaction with other traits. Phenology-related traits (tt_end_of_juvenile, tt_floral_initiation) and water extractability by roots (ll_modifier) displayed such behavior, indicating that impact was likely linked to the level of environmental resources available (water or temperature, in this case), which is expected in these types of environments.

This variance analysis also highlighted expected trait × environment interactions. For instance, a high CO2 concentration triggered the impact of the CO2 response on transpiration efficiency (y_co2_te_modifier). Note that the effect on radiation use efficiency (co2_rue_modifier) was not identified as influential in the TPE (i.e. when no change in CO2; Fig 4) and was thus not included in the further analysis. Also, photoperiodic and vernalization sensitivities (photop_sens, vern_sens) had contrasting effect across sites and sowing dates. These results are consistent with field observations [21].

Trait impacts were related to the availability of environmental resources

Strong interactions were identified between environmental factors and trait impact on yield (Fig 8) for several traits involved in plant development (tt_end_of_juvenile), resource acquisition (ll_modifier), biomass production (y_rue) and biomass allocation (potential_grain_filling_rate) processes. Computed seasonal stress indices for water and nitrogen (see caption of Fig 8) were used to highlight these dependencies between environmental stress and the impact resulting from a trait modification. Modifications in phenology (tt_end_of_juvenile) impacted yield the most in wet environments (stress index near zero), when yield potentials were the greatest (Fig 8A). Nevertheless, this trait had substantial impacts in all environments, including the most severely water limited. Change in water extractability by roots (ll_modifier) also responded to water deficit (Fig 8B) with maximum impacts in severe water deficits. Impacts were slightly less important in mid-early water deficits. They rapidly decreased in less stressed conditions, but remained substantial. Modifications in potential photosynthesis (y_rue) had impacts related to both water and nitrogen availability (Fig 8C). The relation between impact and nitrogen availability was linear within each drought environment type, and the slope of the relation decreased with the severity of the water deficit (i.e. the impact response to N was greater in non-limiting water conditions). Modifications in biomass allocation to grains (potential_grain_filling_rate) led to maximum yield impact in low water deficit (Fig 8D) and in severe nitrogen deficits. Yield impact was increasing with nitrogen deficit but showed a weaker linear correlation in conditions with severe nitrogen stress (r = 0.47).

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Fig 8. Sensitivity index of standardized yield for selected component traits involved in crop development (A), resource acquisition (B), biomass production (C) and biomass allocation (D) relative to seasonal water- or nitrogen-stress indices.

Yield impact was assessed for the thermal time required to reach floral initiation (tt_end_of_juvenile), the water extractability by roots (ll_modifier), the radiation use efficiency (y_rue), and biomass allocation to grains (potential_grain_filling_rate). As sensitivity indices are computed independently for each condition (combinations of sites × year × management), a standardized sensitivity index was used to allow comparison of indices across environments. In this case, simulated yield was standardized () within each of the 9000 environment conditions before computing elementary effects and sensitivity indices (which are always positive in Morris method). The water-stress index [7] indicates the degree to which the soil water extractable by roots (water supply) is able to match the potential crop transpiration (water demand). The nitrogen-stress index is a factor computed by APSIM that determines limiting N level affecting leaf photosynthesis [29]. Both indexes ranged from 0 (no-stress) to 1 (extreme stress). Data are presented for representative drought-pattern environment types (colors), namely “low” (ET1) with stress-free or short-term water-deficits; “mild-late” (ET2) with mild water shortage mainly occurring during grain filling; “mild-early” (ET3) with severe water stress starting during the vegetative stage and relieved during mid-grain filling; and “severe” (ET4) with water deficit from early stages throughout the grain-filling periods [7]. Lines represent linear regressions fitted by environment types.

https://doi.org/10.1371/journal.pone.0146385.g008

Discussion

An in silico method to search for potential candidate traits for breeding

Environmentally-adaptive traits do not scale well from molecular-, organ- or plant-level to the crop level, particularly when targeting yield under stressful conditions [2, 5153]. This difficulty in demonstrating and estimating the impacts of traits across scales potentially limits inference of trait value, and is partly responsible for the non-integration of physiological progress in breeding programs.

Here, the problem was approached in the opposite direction (top-down), to unravel the phenotypic plasticity observed in complex traits into individual trait contribution at the crop level. Process-based crop models are designed to integrate physiological processes and their impact on the local environment (e.g. soil water uptake) based on parameters reflecting plant traits (parameterization), environmental factors and management inputs. As a result, such models simulate genotype × environment interactions and estimate integrated traits (e.g. yield) as emergent properties [1, 2, 22, 54, 55]. Here, the APSIM-Wheat model, which has been widely tested for Australian conditions was used to weigh the impact of numerous plant traits across the Australian wheatbelt, taking into account climatic variability, trait × trait interactions and trait × environment interactions.

While APSIM-Wheat has over 500 parameters with 103 identified as potentially varying with genotype, the approach proposed in this paper allowed the identification of 42 influential traits in the target population of environments (TPE; Fig 4). Of these 42 traits, 23 had an impact that was relatively stable, meaning that the variance of their impact was explained by “controllable” factors (i.e. site, sowing date, nitrogen fertilization and CO2 level) more than those dependent on climate uncertainty.

Overall, the screening phase (sensitivity analysis) allowed the identification of the most influential traits for yield (Figs 46); and the searching phase (variance analysis, relation with specific environmental factors) gave indications as to which traits to target when considering different types of environments within this sample of Australian environments, e.g. high vs low N conditions; Figs 7 and 8. Such an approach could thus help in estimating trait scalability, and give a form of return on investment with an estimation of expected gains from trait modifications. However, additional knowledge is required when considering the potential value for crop breeding (e.g. degree of genotypic variability that may exist for these traits, trait heritability).

Potential candidate traits for improving yield in the Australian wheatbelt

Based on the APSIM-Wheat simulations and a global sensitivity analysis, traits relative to phenology (tt_end_of_juvenile, photop_sens, tt_floral_initiation), resource acquisition (water extraction, ll_modifier and light interception, y_extinct_coef), resource use efficiency (y_rue, transp_efficiency_coef) and biomass allocation to the grain (potential_grain_filling_rate, grains_per_gram_stem) were among the most important traits in the TPE, assuming a “genetic” variation of ± 20% around trait value of the reference cultivar Hartog (Fig 4). It is important to keep in mind that the results of a sensitivity analysis strongly depend on the chosen range of trait variation, and that the ± 20% trait variation used in this study under-estimated existing variations for some traits (e.g. vern_sens) while it may have over-estimated unknown variations in others. However, assuming that (1) the APSIM model behaves relatively linearly (interaction:main effect ratio of 1-1.5 for most parameters, Fig 4) and (2) new interactions do not arise from this extension in the parameter ranges, a moderate change of this range would not have strongly affected the estimated impacts (main effect), i.e. the most influent traits have correctly been identified in this study. Overall, the approach allowed a first screening of a wide range of traits for which the range of genetic variability is unknown. This work could be improved in the future through the incorporation of knowledge on genetic variability of selected traits. Adjustments on the TPE could also be investigated, for instance, TPE for future climate scenarios could be explored to identify potential traits of future importance, providing crop models can properly deal with these future conditions.

The most important trait in terms of impact on yield was the water extractability by roots (ll_modifier; Figs 4 and 5), especially in Narrabri and Yanco, which had heavy deep soils and thus a high water-holding capacity (Fig 6). Genotypic variation in water extractability at depth was observed in root chambers by Manschadi et al. [50], who assessed that this trait could bring about an extra 50 kg ha-1 for every mm of water extracted during the grain filling period, for crops grown in the north-eastern part of the wheatbelt (i.e. ability to extract more water late in the season has a high marginal value in terminal stress environments). Compared to other root-related traits, Veyradier et al. [56] found that this trait was a strong candidate for breeding purpose in terms of potential impact. Field experiments for two cultivars with contrasting water extractability at depth also highlighted the potential of this trait to improve yield in drought-prone conditions [50, 57], which agrees with the increasing yield impact simulated for increasing drought severity (Fig 8B).

Several traits involved in wheat development were identified as playing a major role in crop performance in the TPE (Figs 46). Traits related to phenology are usually considered as the primary means to adapt crops to their growing environments [58, 59]. Recently, an association mapping study [60] focused on three traits (earliness per se, photoperiod sensitivity and vernalization requirement), whose corresponding parameters in APSIM-Wheat model (tt_end_of_juvenile, photop_sens and vern_sens, respectively) were ranked among the most influential ones in this study (i.e. average main impacts on yield respectively of 0.72, 0.62 and 0.04 t ha-1), despite the fact that our reference cultivar (Hartog) has a low vernalization requirement (vern_sens of 1.5). These three traits were found to vary in the ranges of 515-980°Cd, 0-4.1 and 0-2.9 respectively for a broad range of Australian cultivars [21], which is substantially greater than the range tested here (444-666°Cd, 2.4-3.6 and 1.2-1.8), especially for the vernalization requirement. The relative importance of those traits on yield is expected to change when changing their range of variation. In particular, vern_sens is expected to have a greater impact in the TPE, as found by Zhao et al. [36] who tested a range of 0-5 for this trait in a similar analysis. Also, unsurprisingly, these three traits were found to be strongly dependent on the site and sowing date (Fig 7) but had a high level of variations (high residuals in Fig 7), which is likely related to interactions with stresses.

Other traits had a strong impact on yield. The most important of these include: (1) the potential RUE (y_rue) which is a major target for current research projects aiming to improve photosynthesis efficiency [6164], (2) plant architecture (y_extinct_coef) which has been of interest to some breeders (e.g. durum-wheat CIMMYT) who have selected for erect wheat genotypes [65], and (3) the potential grain filling rate (potential_grain_filling_rate), which may be improved by the current efforts of breeders and pre-breeders selecting for stay-green phenotype [6668], cooler canopy temperature [59, 69, 70], greater reserve remobilisation [71, 72] and/or greater spike photosynthesis [73, 74].

The importance of properly considering the target population of environments

Depending on the environment/management conditions considered, the ranking of trait main impacts varied across traits (Fig 6), thus highlighting the need to appropriately consider trait effects across the target populations of environments [75]. For instance, the sensitivity to photoperiod (photop_sens) had a small impact in Emerald but an important impact in Narrabri and Yanco (Fig 6C). Hence, while most influential parameters by Zhao et al. [36] were also identified as the most influential subset in our study, the discrepancies in trait impact between these two studies partly rose from differences in conditions considered (e.g. sowing dates, fertilization, plant density). Our study also explored climate change impacts on the 42 influential traits and indicated that traits of most value may change in the future, as illustrated for the impact of transpiration-efficiency response to CO2 (y_co2_te_modifier) under different levels of CO2 (Fig 7). Note that other traits such as radiation-use-efficiency response to CO2 (co2_rue_modifier), which had only minor impact in current climates (Fig 4) and were thus not studied in detail, are likely to have a substantial impact in the future.

The importance of considering trait combinations rather than single traits

Sadras and Richards [52] argued and illustrated how indirect breeding methods often fail to improve yield not because yield is complex, but rather because those methods do not account for the proper levels of organization, time scales and interactions among traits and with the environment. Similarly, trait impacts in crops subjected to multiple stresses (e.g. nitrogen and water limitation) are rarely considered in traditional physiological approaches [52]. Working with an integrative crop model, we illustrated in this paper how the potential value of traits, in combination with others and for a specific TPE, can be assessed in silico by testing (1) whether the trait is likely to impact crop performance (e.g. estimation of main sensitivity index), (2) if this impact is modified by controllable (management) or uncontrollable (climate, genotype × environment interactions) factors, and (3) how the trait impact is distributed among environment-type of importance for the TPE [7].

The systematic presence of interaction effects found with the sensitivity analysis (Fig 4) illustrated that trait interactions are common. Such results highlight the importance of focusing on collections of traits rather on individual traits [76].

Furthermore, although of high importance, links among carbon, water, and nitrogen transfers within crops are experimentally difficult to assess due to their genetic, physiologic, and agronomic complexities. For instance, efficiencies in water- and nitrogen-use can be either unrelated, positively (synergy) or negatively (trade-off) related depending on the environment, the genotype, the level of organization, and the time scale at which such efficiencies are defined [52, 77, 78].

Overall, the complexity of crop systems highlights the potential benefit of using modeling approaches. Together with genetic criteria (e.g. availability of genetic variability, pleiotropy and heritability) and technical criteria (rapid, cost-effective, and reliable phenotyping), model-based approaches (assuming the relevance of the process-based model, of the genetic range tested and of the TPE) could help breeding to improve crop performance under changing environments [2, 52].

A tool to overview and improve crop models

From a modeling point of view, crop models are evolving over time, while physiological knowledge underlying crop functioning gradually improves. Model improvements are thus regularly performed with algorithm modifications being tracked over time. However, the effects of such modifications on the model-prediction capacity are usually not clearly documented nor shared among all model users and developers. Hence, with different developers focusing simultaneously or successively on a model, there is a high risk of developing increasingly complex and harder to understand algorithms. Problems caused by this increased complexity may affect the quality of the model, but may be revealed and addressed by using exploration methods throughout model-development phases to visualize the in-progress modeling state. Systems analyses, as done in this paper can for instance enable developers to quickly assess changes in model response due to variation in specific processes, and notice potential problems.

In this study, we attempted to consider the maximum proportion of traits utilized in APSIM-Wheat. The use of function-table parameters in APSIM complicated the estimation of the total number of values used as parameters and the assessment of individual parameter impact on output variables. Overall, about half of the plant-related parameters of APSIM-Wheat had no impact, keeping in mind that those parameters may be useful for other crops, or other processes (e.g. responses to high-temperature or soil minerals). While using a global sensitivity analysis to identify such parameters may appear as an excessive method, the computational cost to include all parameters (with null, low or high impact) was lower than the time and expertise needed to analyze the source code and manually identify subsets of parameters, in the case of this complicated crop model.

In total, 42 parameters were identified as influential, as they had an average main impact greater than 20 kg ha-1 in the TPE. However, only 5 parameters had a mean impact greater than 50 kg ha-1. Martre et al. [76] proposed physiological reasons to explain such a surprisingly low number of influential parameters in crop models: (1) number of trade-offs occur with traits often having compensating effects when scaling up from plant to crop level (e.g. once canopies are well established, increasing the leaf surface area may not improve light interception and thus photosynthesis) and (2) the fact that complex characters such as grain yield and protein concentration are inherently determined at the population level rather than at the organ or plant level [79]. While model over-parameterization can result from model development as well as model design, indicators can help to track the model complexity and performance. In this context, the use of the exploration methods described here provides an overview of the model global response to perturbation (e.g. Figs 35).

Finally, such sensitivity analysis can help to identify traits most important for parameter calibration for cultivars [36]. Such targeted calibration can later be implemented with either frequentist [80] or Bayesian parameter estimation algorithms [81].

Conclusion

Phenotyping and breeding strategies can be improved by better understanding the yield-trait performance landscapes [82]. We performed a Morris global sensitivity analysis on the APSIM-Wheat model to assess the impact of 90 physiological traits on yield for Australian rain-fed wheat crops. The genotype × environment × management (G×E×M) landscape was explored using 82 million individual simulations for the target population of environments (TPE), combining a factorial design for the environment × management effects and a Morris sampling design for APSIM trait parameters. Our analysis highlights 42 parameters substantially impacting yield in most of the TPE. Among those, a few parameters related to phenology, resource acquisition, resource use efficiency and biomass allocation were identified as potential candidates for crop improvement.

As a final conclusion, the integration of G×E×M interactions through modeling approaches is an increasingly topical consideration to help prioritizing investments of research efforts for the benefit of breeding [17]. However, newly-gained computational knowledge has to be constantly confronted to physiological reality in order to determine the complexity of G×E×M interactions that impede progress in crop productivity.

Supporting Information

S1 Fig. Range of variation used for function parameters.

Each graph represents one function parameter (x and y vectors), except for grouped parameters (i.e. leaf, stem and pod nitrogen demand). The graph titles match the Process column in S1 Table. Nominal values are indicted in green, while minimum and maximum values are displayed blue and red, respectively. As some parameters were grouped to be modified together, different symbols are used for related processes (maximum, critical and minimum nitrogen content) as defined in APSIM-wheat [29].

https://doi.org/10.1371/journal.pone.0146385.s001

(PDF)

S1 Table. Description of the APSIM-wheat parameters included in the sensitivity analysis.

Module refers to the sub-model where the parameter is used in APSIM-wheat, Process refers to the physiological process targeted by the considered parameter and Factor is the parameter name used in the present study and in the APSIM documentation [29], where a complete description of the parameters is given. The Default Value field lists the nominal value of the parameter for cultivar Hartog in APSIM-wheat 7.5 (only first three values were presented when the parameter is defined as a vector). In the Process field, influential parameters in indicated in bold and parameters that were grouped together for physiologic reasons are identified by (*).

https://doi.org/10.1371/journal.pone.0146385.s002

(PDF)

Author Contributions

Conceived and designed the experiments: PC KC SC RF. Performed the experiments: PC BZ SC KC. Analyzed the data: PC KC BZ SC NH. Contributed reagents/materials/analysis tools: BZ RF. Wrote the paper: PC BZ SC NH RF KC.

References

  1. 1. Chapman S, Cooper M, Hammer G. Using crop simulation to generate genotype by environment interaction effects for sorghum in water-limited environments. Australian Journal of Agricultural Research. 2002;53: 379–389.
  2. 2. Hammer G, Cooper M, Tardieu F, Welch S, Walsh B, Eeuwijk F van, et al. Models for navigating biological complexity in breeding improved crop plants. Trends in Plant Science. 2006;11: 587–593. pmid:17092764
  3. 3. Chapman S. Use of crop models to understand genotype by environment interactions for drought in real-world and simulated plant breeding trials. Euphytica. Springer; 2008;161: 195–208.
  4. 4. Chapman SC, Chakraborty S, Dreccer MF, Howden SM. Plant adaptation to climate change—opportunities and priorities in breeding. Crop and Pasture Science. CSIRO; 2012;63: 251–268.
  5. 5. Zheng B, Chenu K, Fernanda Dreccer M, Chapman SC. Breeding for the future: What are the potential impacts of future frost and heat events on sowing and flowering time requirements for australian bread wheat (Triticum aestivium) varieties? Global Change Biology. Wiley Online Library; 2012;18: 2899–2914. pmid:24501066
  6. 6. Chenu K, Cooper M, Hammer G, Mathews K, Dreccer M, Chapman S. Environment characterization as an aid to wheat improvement: Interpreting genotype–environment interactions by modelling water-deficit patterns in North-Eastern Australia. Journal of Experimental Botany. Soc Experiment Biol; 2011;62: 1743–1755. pmid:21421705
  7. 7. Chenu K, Deihimfard R, Chapman SC. Large-scale characterization of drought pattern: A continent-wide modelling approach applied to the Australian wheatbelt–spatial and temporal trends. New Phytologist. Wiley Online Library; 2013;198: 801–820. pmid:23425331
  8. 8. Ortiz-Monasterio R, Sayre K, Rajaram S, McMahon M, others. Genetic progress in wheat yield and nitrogen use efficiency under four nitrogen rates. Crop Science. Crop Science Society of America; 1997;37: 898–904.
  9. 9. Richards R, Hunt J, Kirkegaard J, Passioura J. Yield improvement and adaptation of wheat to water-limited environments in Australia- a case study. Crop and Pasture Science. CSIRO; 2014;65: 676–689.
  10. 10. Yang R-C, Blade SF, Crossa J, Stanton D, Bandara MS. Identifying isoyield environments for field pea production. Crop Science. Crop Science Society of America; 2005;45: 106–113.
  11. 11. Vega A de la, DeLacy I, Chapman S. Changes in agronomic traits of sunflower hybrids over 20 years of breeding in central Argentina. Field Crops Research. Elsevier Science Bv; 2007;100: 73–81.
  12. 12. Chapman SC, Cooper M, Butler DG, Henzell RG. Genotype by environment interactions affecting grain sorghum. I. Characteristics that confound interpretation of hybrid yield. Aust J Agric Res. 2000;51: 197–208. Available: http://www.publish.csiro.au/paper/AR99020.
  13. 13. Cooper M, Woodruff DR, Eisemann RL, Brennan PS, DeLacy IH. A selection strategy to accommodate genotype-by-environment interaction for grain yield of wheat: Managed-environments for selection among genotypes. TAG Theoretical and Applied Genetics. 1995;90: 492–502. Available: http://dx.doi.org/10.1007/BF00221995. pmid:24173943
  14. 14. Mathews KL, Chapman SC, Trethowan R, Pfeiffer W, Van Ginkel M, Crossa J, et al. Global adaptation patterns of Australian and CIMMYT spring bread wheat. Theoretical and Applied Genetics. Springer; 2007;115: 819–835. pmid:17768603
  15. 15. Chapman SC, Crossa J, Edmeades GO. Genotype by environment effects and selection for drought tolerance in tropical maize. I. Two mode pattern analysis of yield. Euphytica. Springer; 1997;95: 1–9.
  16. 16. Alwala S, Kwolek T, McPherson M, Pellow J, Meyer D. A comprehensive comparison between Eberhart and Russell joint regression and GGE biplot analyses to identify stable and high yielding maize hybrids. Field Crops Research. Elsevier; 2010;119: 225–230.
  17. 17. Hammer GL, McLean G, Chapman S, Zheng B, Doherty A, Harrison MT, et al. Crop design for specific adaptation in variable dryland production environments. Crop and Pasture Science. CSIRO; 2014;65: 614–626.
  18. 18. Nyquist WE, Baker R. Estimation of heritability and prediction of selection response in plant populations. Critical reviews in plant sciences. Taylor & Francis; 1991;10: 235–322.
  19. 19. Cooper M, Stucker R, DeLacy I, Harch B. Wheat breeding nurseries, target environments, and indirect selection for grain yield. Crop Science. Crop Science Society of America; 1997;37: 1168–1176.
  20. 20. Chapman S, Cooper M, Podlich D, Hammer G. Evaluating Plant Breeding Strategies by Simulating Gene Action and Dryland Environment Effects. Agronomy Journal. 2003;95: 99–113. Available: http://agron.scijournals.org/cgi/content/abstract/agrojnl;95/1/99.
  21. 21. Zheng B, Biddulph B, Li D, Kuchel H, Chapman S. Quantification of the effects of VRN1 and Ppd-D1 to predict spring wheat (Triticum aestivum) heading time across diverse environments. Journal of Experimental Botany. Soc Experiment Biol; 2013;64: 3747–3761. pmid:23873997
  22. 22. Chenu K, Chapman S, Tardieu F, McLean G, Welcker C, Hammer G. Simulating the yield impacts of organ-level quantitative trait loci associated with drought response in maize: A“gene-to-phenotype” modeling approach. Genetics. Genetics Soc America; 2009;183: 1507. pmid:19786622
  23. 23. Jeuffroy M-H, Casadebaig P, Debaeke P, Loyce C, Meynard J-M. Agronomic model uses to predict cultivar performance in various environments and cropping systems. a review. Agronomy for Sustainable Development. Springer Paris; 2014;34: 121–137.
  24. 24. Rebetzke GJ, Chenu K, Biddulph B, Moeller C, Deery DM, Rattey AR, et al. A multisite managed environment facility for targeted trait and germplasm phenotyping. Functional Plant Biology. CSIRO; 2013;40: 1–13.
  25. 25. Potgieter A, Hammer G, Butler D. Spatial and temporal patterns in Australian wheat yield and their relationship with ENSO. Crop and Pasture Science. CSIRO; 2002;53: 77–89.
  26. 26. Williams J, Hamblin AP, Hook RA. Agro-ecological regions of Australia. Methodologies for their derivation and key issues in resource management. CSIRO Land; Water; 2002.
  27. 27. Keating BA, Carberry PS, Hammer GL, Probert ME, Robertson MJ, Holzworth D, et al. An overview of APSIM, a model designed for farming systems simulation. European Journal of Agronomy. 2003;18: 267–288.
  28. 28. Holzworth DP, Huth NI, deVoil PG, Zurcher EJ, Herrmann NI, McLean G, et al. APSIM—Evolution towards a new generation of agricultural systems simulation. Environmental Modelling & Software. 2014;62: 327–350.
  29. 29. Zheng B, Chenu K, Doherty A. The APSIM-Wheat Module (7.5 R3008) [Internet]. CSIRO; 2014. Available: www.apsim.info.
  30. 30. Wang J, Wang E, Luo Q, Kirby M. Modelling the sensitivity of wheat growth and water balance to climate change in Southeast Australia. Climatic Change. Springer; 2009;96: 79–96.
  31. 31. Saltelli A, Chan K. Sensitivity Analysis. Scott EM, editor. Wiley; 2000.
  32. 32. Monod H, Naud C, Makowski D. Working with dynamic crop models, evaluation, analysis, parameterization and applications. In: Wallach D, Makowski D, Jones JW, editors. Elsevier; 2006. pp. 55–100.
  33. 33. Valade A, Ciais P, Vuichard N, Viovy N, Caubel A, Huth N, et al. Modeling sugarcane yield with a process-based model from site to continental scale: Uncertainties arising from model structure and parameter values. Geoscientific Model Development. 2014;7: 1225–1245.
  34. 34. Da Silva D, Han L, Faivre R, Costes E. Influence of the variation of geometrical and topological traits on light interception efficiency of apple trees: Sensitivity analysis and metamodelling for ideotype definition. Annals of botany. Annals Botany Co; 2014;114: 739–752. pmid:24723446
  35. 35. Martre P, He J, Le Gouis J, Semenov MA. In silico system analysis of physiological traits determining grain yield and protein concentration for wheat as influenced by climate and crop management. Journal of Experimental Botany. Soc Experiment Biol; 2015; erv049.
  36. 36. Zhao G, Bryan BA, Song X. Sensitivity and uncertainty analysis of the APSIM-wheat model: Interactions between cultivar, environmental, and management parameters. Ecological Modelling. Elsevier; 2014;279: 1–11.
  37. 37. Morris MD. Factorial sampling plans for preliminary computational experiments. Technometrics. Taylor & Francis; 1991;33: 161–174.
  38. 38. Campolongo F, Cariboni J, Saltelli A. An effective screening design for sensitivity analysis of large models. Environmental Modelling & Software. Elsevier; 2007;22: 1509–1518.
  39. 39. Wang E, Robertson M, Hammer G, Carberry P, Holzworth D, Meinke H, et al. Development of a generic crop model template in the cropping system model APSIM. European Journal of Agronomy. Elsevier; 2002;18: 121–140.
  40. 40. Zheng B, Holland E, Chapman S. Wheat modelling: A case study in innovating across CSIRO Grid computing systems. eResearch Australasia Brisbane, Australia. 2013;
  41. 41. Zomer RJ, Trabucco A, Bossio DA, Verchot LV. Climate change mitigation: A spatial analysis of global land suitability for clean development mechanism afforestation and reforestation. Agriculture, Ecosystems & Environment. Elsevier; 2008;126: 67–80.
  42. 42. Iooss B, Lemaître P. A review on global sensitivity analysis methods. arXiv preprint arXiv:14042405. 2014;
  43. 43. R Core Team. R: A language and environment for statistical computing [Internet]. Vienna, Austria: R Foundation for Statistical Computing; 2014. Available: http://www.R-project.org/.
  44. 44. Wickham H, Francois R. dplyr: A grammar of data manipulation [Internet]. 2015. Available: http://CRAN.R-project.org/package = dplyr.
  45. 45. Pujol G, Iooss B, Paul Lemaitre AJ with contributions from, Gilquin L, Gratiet LL, Touati T, et al. Sensitivity: Sensitivity analysis [Internet]. 2014. Available: http://CRAN.R-project.org/package = sensitivity.
  46. 46. Wickham H. ggplot2: Elegant graphics for data analysis [Internet]. Springer New York; 2009. Available: http://had.co.nz/ggplot2/book.
  47. 47. Poorter H, Evans JR. Photosynthetic nitrogen-use efficiency of species that differ inherently in specific leaf area. Oecologia. Springer; 1998;116: 26–37.
  48. 48. Poorter H, Garnier E. Ecological significance of inherent variation in relative growth rate and its components. Handbook of functional plant ecology. Marcel Dekker New York; 1999;20: 81–120.
  49. 49. Poorter H, Niinemets Ü, Poorter L, Wright IJ, Villar R. Causes and consequences of variation in leaf mass per area (LMA): A meta-analysis. New Phytologist. Wiley Online Library; 2009;182: 565–588. pmid:19434804
  50. 50. Manschadi AM, Christopher J, Hammer GL, others. The role of root architectural traits in adaptation of wheat to water-limited environments. Functional Plant Biology. CSIRO; 2006;33: 823–837.
  51. 51. Chapman SC, Hammer GL, Podlich DW, Cooper M. Quantitative genetics, genomics and plant breeding. In: Kang , editor. CAB International, Wallingford UK; 2002. pp. 167–187.
  52. 52. Sadras V, Richards R. Improvement of crop yield in dry environments: Benchmarks, levels of organisation and the role of nitrogen. Journal of Experimental Botany. Soc Experiment Biol; 2014;65: 1981–1995. pmid:24638898
  53. 53. Rebetzke GJ, Fischer RTA, Herwaarden AF van, Bonnett DG, Chenu K, Rattey AR, et al. Plot size matters: Interference from intergenotypic competition in plant phenotyping studies. Functional Plant Biology. CSIRO; 2014;41: 107–118.
  54. 54. Bertin N, Martre P, Genard M, Quilot B, Salon C. Under what circumstances can process-based simulation models link genotype to phenotype for complex traits? Case-study of fruit and grain quality traits. Journal of Experimental Botany. Soc Experiment Biol; 2010;61: 955–967. pmid:20038518
  55. 55. Yin X, Struik PC. Modelling the crop: From system dynamics to systems biology. Journal of Experimental Botany. Soc Experiment Biol; 2010;61: 2171–2183. pmid:20051352
  56. 56. Veyradier M, Christopher J, Chenu K. Quantifying the potential yield benefit of root traits. In: Sievänen R, Nikinmaa E, Godin C, Lintunen A, Nygren P, editors. Proceedings of the 7th international conference on Functional-Structural Plant Models, Saariselkä, Finland, 9-14 June. 2013. pp. 317–319.
  57. 57. Christopher J, Manschadi A, Hammer G, Borrell A. Developmental and physiological traits associated with high yield and stay-green phenotype in wheat. Crop and Pasture Science. CSIRO; 2008;59: 354–364.
  58. 58. Snape J, Butterworth K, Whitechurch E, Worland A. Waiting for fine times: Genetics of flowering time in wheat. Euphytica. Springer; 2001;119: 185–190.
  59. 59. Reynolds M, Foulkes MJ, Slafer GA, Berry P, Parry MA, Snape JW, et al. Raising yield potential in wheat. Journal of Experimental Botany. Soc Experiment Biol; 2009;60: 1899–1918. pmid:19363203
  60. 60. Bogard M, Ravel C, Paux E, Bordes J, Balfourier F, Chapman S, et al. Predictions of heading date in bread wheat (Triticum aestivum L.) using QTL-based parameters of an ecophysiological model. Journal of Experimental Botany. Soc Experiment Biol; 2014;65: 5849–5865. pmid:25148833
  61. 61. Richards RA. Selectable traits to increase crop photosynthesis and yield of grain crops. Journal of Experimental Botany. 2000;51: 447–458. pmid:10938853
  62. 62. Parry MA, Reynolds M, Salvucci ME, Raines C, Andralojc PJ, Zhu X-G, et al. Raising yield potential of wheat. II. Increasing photosynthetic capacity and efficiency. Journal of Experimental Botany. Soc Experiment Biol; 2010; erq304.
  63. 63. Zhu X-G, Long SP, Ort DR. Improving photosynthetic efficiency for greater yield. Annual review of plant biology. Annual Reviews; 2010;61: 235–261. pmid:20192734
  64. 64. Reynolds M, Foulkes J, Furbank R, Griffiths S, King J, Murchie E, et al. Achieving yield gains in wheat. Plant, Cell & Environment. Wiley Online Library; 2012;35: 1799–1823.
  65. 65. Fischer R. Increasing yield potential in wheat: Breaking the barriers. In: Reynolds M, Rajaram S, McNab A, editors. Workshop Proc. Cd. Obregon, Mexico, CIMMYT. 1996. pp. 150–166.
  66. 66. Lopes M, Reynolds M, Manes Y, Singh R, Crossa J, Braun H. Genetic yield gains and changes in associated traits of CIMMYT spring bread wheat in a “historic” set representing 30 years of breeding. Crop Science. The Crop Science Society of America, Inc. 2012;52: 1123–1131.
  67. 67. Yang D, Luo Y, Ni Y, Yin Y, Yang W, Peng D, et al. Effects of exogenous ABA application on post-anthesis dry matter redistribution and grain starch accumulation of winter wheat with different staygreen characteristics. The Crop Journal. Elsevier; 2014;2: 144–153.
  68. 68. Christopher JT, Veyradier M, Borrell AK, Harvey G, Fletcher S, Chenu K. Phenotyping novel stay-green traits to capture genetic variation in senescence dynamics. Functional Plant Biology. CSIRO; 2014;41: 1035–1048.
  69. 69. Babar M, Reynolds M, Van Ginkel M, Klatt A, Raun W, Stone M. Spectral reflectance to estimate genetic variation for in-season biomass, leaf chlorophyll, and canopy temperature in wheat. Crop Science. Crop Science Society of America; 2006;46: 1046–1057.
  70. 70. Pinto RS, Reynolds MP, Mathews KL, McIntyre CL, Olivares-Villegas J-J, Chapman SC. Heat and drought adaptive QTL in a wheat population designed to minimize confounding agronomic effects. Theoretical and Applied Genetics. Springer; 2010;121: 1001–1021. pmid:20523964
  71. 71. Rebetzke G, Condon A, Farquhar G, Appels R, Richards R. Quantitative trait loci for carbon isotope discrimination are repeatable across environments and wheat mapping populations. Theoretical and Applied Genetics. Springer; 2008;118: 123–137. pmid:18818897
  72. 72. Dreccer MF, Herwaarden AF van, Chapman SC. Grain number and grain weight in wheat lines contrasting for stem water soluble carbohydrate concentration. Field Crops Research. Elsevier; 2009;112: 43–54.
  73. 73. Abbad H, El Jaafari S, Bort J, Araus J. Comparative relationship of the flag leaf and the ear photosynthesis with the biomass and grain yield of durum wheat under a range of water conditions and different genotypes. Agronomie. 2004;24.
  74. 74. Tambussi EA, Bort J, Guiamet JJ, Nogués S, Araus JL. The photosynthetic role of ears in C3 cereals: Metabolism, water use efficiency and contribution to grain yield. Critical Reviews in Plant Sciences. Taylor & Francis; 2007;26: 1–16.
  75. 75. Chenu K. Characterising the crop environment–nature, significance and applications. In: Sadras V, Calderini D, editors. Academic Press; 2015. pp. 321–348.
  76. 76. Martre P, Quilot-Turion B, Luquet D, Memmah M-MO-S, Chenu K, Debaeke P. Crop physiology: Applications for genetic improvement and agronomy. In: Sadras VO, Calderini D, editors. Academic Press; 2015.
  77. 77. Cabrera-Bosquet L, Molero G, Bort J, Nogués S, Araus J. The combined effect of constant water deficit and nitrogen supply on WUE, NUE and Δ13C in durum wheat potted plants. Annals of Applied Biology. Wiley Online Library; 2007;151: 277–289.
  78. 78. Sadras V, Rodriguez D. Modelling the nitrogen-driven trade-off between nitrogen utilisation efficiency and water use efficiency of wheat in eastern Australia. Field Crops Research. Elsevier; 2010;118: 297–305.
  79. 79. Sinclair TR, Purcell LC, Sneller CH. Crop transformation and the challenge to increase yield potential. Trends in Plant Science. 2004;9: 70–75. Available: http://www.sciencedirect.com/science/article/B6TD1-4BDY672-1/2/ce7457061a36a8af382e9dbce6764d47. pmid:15102372
  80. 80. Wallach D, Buis S, Lecharpentier P, Bourges J, Clastre P, Launay M, et al. A package of parameter estimation methods and implementation for the STICS crop-soil model. Environmental Modelling & Software. Elsevier; 2011;26: 386–394.
  81. 81. Dumont B, Leemans V, Mansouri M, Bodson B, Destain J-P, Destain M-F. Parameter identification of the STICS crop model, using an accelerated formal MCMC approach. Environmental Modelling & Software. Elsevier; 2014;52: 121–135.
  82. 82. Messina CD, Podlich D, Dong Z, Samples M, Cooper M. Yield–trait performance landscapes: From theory to application in breeding maize for drought tolerance. Journal of Experimental Botany. Soc Experiment Biol; 2011;62: 855–868. pmid:21041371