1. Introduction
Forage planting has expanded in recent years worldwide to ensure meat and milk production. Tropical pastures consisting of grasses and legumes represent the most economical source of nutrients for livestock [
1]. Ryegrass (
Lolium perenne L.) is a plant species widely used in intensively managed pasture-based ruminant husbandry systems due to its ease of establishment, high digestibility, and balanced seasonal dry matter production [
2]. Lolium perenne is a caespitose plant up to 80 cm in height, which produces a variable amount of tillers throughout its life. Its leaves are glabrous and have lamellae that are between 20 to 30 cm long and up to 6 mm wide. The prefoliation is conduplicate or folded. Ryegrass is a hardy and very tough species; it resprouts quickly and has a good robust rooting system, which makes it less susceptible to trampling and useful for early establishment of short- and long-term pastures. However, ryegrass crop establishment is severely affected by low water availability as well as soil nutrient deficiency [
3,
4].
Cattle production in Colombia in the high tropics (>2000 m.a.s.l) is characterized by the use of fodder such as ryegrass (
Lolium perenne L.) as the basis of their diet; these areas contribute 32% of the national production of milk and meat. In Colombia, milk production accounts for 12% of agricultural GDP and generates 20% of agricultural employment; 17% of agricultural units produce milk [
5]. Nevertheless, productivity is low and not comparable to that of the main milk and meat producing countries in the world; water availability and soil conservation are essential elements to take advantage of the forage potential of Colombia’s high tropics and improve productivity.
There is increasing uncertainty regarding water availability for agriculture. Agriculture uses up to 70% of global freshwater withdrawals, making it the largest consumer of water. The response of grasslands to drought depends on the duration, intensity, and timing of the drought, as well as the frequency of rainfall [
6]. It also depends on the interactions between different factors, including diversity of the plant community, soil properties, climatic conditions, and land management [
7]. Grassland productivity is expected to be affected by climate change [
8,
9]; however, there is great uncertainty regarding the biomass productivity of grasslands in tropical regions under changing climatic conditions. The Institute of Hydrology, Meteorology and Environmental Studies of Colombia predicted increases in the country’s average temperature of 0.9 °C, 1.6 °C, and 2.14 °C for 2040, 2070, and 2100, respectively, and a decrease in rainfall of between 10% and 40% in a third of the country (mainly in the Andean zone and the high tropics of Colombia) [
10]. Farmers can adapt to climate variability by choosing different grass species or cultivars and adjusting management practices, such as irrigation application strategies and selection of planting and harvest dates.
Most of the models adapted for the cultivation of perennial ryegrass have been developed for cold temperate climatic conditions in Nordic countries. In addition, the simulations of biomass accumulation are a function of temperature and light availability, and this limits their accuracy in predicting pasture productivity in tropical and subtropical regions. The models that have so far been used to model the biomass of perennial ryegrass are BASGRA [
11], LINGRA [
12], and PaSIM [
13]; these models were designed to simulate the dynamics of grass monocultures in Norway and Finland during successive years and under repeated defoliation. In these three models, biomass accumulation is based on the concept of radiation use efficiency, where inter-accepted solar radiation is converted to biomass. These are typically complex models and require numerous input parameters.
Some well-known models have already been adapted with satisfactory results for tropical pastures and forage: the AgPasture model [
14,
15], integrated in the APSIM package (‘The Agricultural Production Systems sIMulator’) simulates mixed C3 and C4 grass and legume pastures; APSIM-Growth [
16] simulates the growth of tropical pastures as a function of radiation use efficiency; APSIM-Tropical Pasture [
17] was used to simulate Brachiaria brizantha growth; CROPGRO-PFM [
18,
19,
20] is a mechanistic model of the Decision Support System for Agrotechnology Transfer (DSSAT) platform, to simulate forage production and has been widely explored in Brazil.
In this context, the Food and Agriculture Organization of the United Nations (FAO) developed the AquaCrop simulation model to assist consultants, irrigation engineers, agronomists, (non-)governmental organizations, and even farm managers with the formulation and evaluation of guidelines for increasing crop water productivity with improved agronomic practices [
21].
In the AquaCrop model, the biophysical processes are simplified so that the amount of data required for input and calibration remains limited, while robustness and accuracy are protected [
22]. The AquaCrop model was initially developed for herbaceous food crops, although forage crops are now being considered [
23,
24,
25]. A growing community of AquaCrop users is continuously adding new crops. Simulation models for tropical grasses can benefit forage researchers and farm managers by improving forage production systems in tropical regions as well as providing information in climate variability scenarios on yield gaps and production risk analysis.
This study aims to calibrate and validate the AquaCrop model for Perennial ryegrass (Lolium perenne L.) in the Colombian high tropics. Therefore, we use experimental field data collected in two cropping seasons to generate the parameter crop file required to run a simulation with the AquaCrop model.
2. Materials and Methods
2.1. AquaCrop Model Description
The Food and Agriculture Organization of the United Nations—FAO—developed the AquaCrop model [
26]. AquaCrop uses the water productivity as a growth driver. The model requires field-level observations and provides a reasonable compromise between detailed, targeted crop yield simulation models and simplistic experimental models with considerable accuracy, robustness, and user-friendliness [
23]. Model inputs include climate observations, different field data including soil profile, irrigation and farm management practices, and crop phenological growth stages in terms of their thermal time or calendar day requirements.
The AquaCrop model calculates the daily water balance by separating transpiration and evaporation. Transpiration and evaporation are correlated with the area of vegetated and unvegetated ground cover, respectively. Plant response to water stress is modelled as a function of leaf expansion, stomatal conductance, early canopy senescence, and change in harvest index. Subsequently, the model simulates the yield and biomass from daily transpiration values (Equations (1) and (2)).
where
B = above ground biomass (t ha
−1),
WP = water productivity (kg m
−3),
Tr = crop transpiration (m
3 ha
−1),
HI = harvest index, and
Y = yield (t ha
−1).
FAO recently published the new version of AquaCrop (V. 7.0), in which new advances were introduced; the most important is the module to simulate the growth and production of perennial herbaceous forage crops, as tested with alfalfa. In addition, its procedures include describing reduction of plant population over time, the translocation of nutrients from the canopy to the root system from season to season, the growth of the canopy and forage crop management between cutting events, the programming of the cuts and the number of them within the growth cycle in the medium and long term, and the calculation of the ET
0 based on the climate information introduced in the model [
27]. The new version of AquaCrop 7.0 considers the transfer of nutrients from the canopy to the root system of the crop, which usually occurs after the middle of the annual season in perennial herbaceous forage crops; this fraction can be considerable. When the following season begins, the fraction of the nutrients stored in the roots is mobilized towards the crop canopy. The model assumes that part of the nutrients is lost during the low respiration season and due to the natural reduction of the canopy or remains stored in the roots. The new module for perennial herbaceous forage crops considers several cuts during their growth and development. The users can program or generate the harvests according to their cuts within some criteria [
28].
2.2. Study Site
Two field experiments were conducted in the growing seasons of 2008 to 2010 in equatorial highland zones of Colombia at the Colombian Corporation of Agricultural Research (AGROSAVIA), Tibaitatá Research Center, Colombia (4°42′ N; 74°12′ W; 2543 m a.s.l.). Long-term climate data from the Tibaitata Research Center (1954–2020) shows rainfall of approximately 657 mm per year on average, concentrated in the winter (March–July and October–November). Moreover, the average maximum temperature in January is 16.4 °C, and the minimum temperature is about 9.7 °C. The mean relative humidity is 77.9–83.8%, and the average daily reference evapotranspiration is 2.83 mm day−1.
2.3. Experimental Setup and Irrigation Water Management
The fields trials were conducted during two successive growing seasons: the first (used for calibration of the AquaCrop model) spanned from 19 December 2008 until 2 February 2010. The second growing season (used for AquaCrop model validation) spanned from 10 February 2010 until 7 October 2010. The field experiments were conducted on a 36 m by 40 m plot, and the soil of the experimental site is an Andisol with a silty loam texture.
The perennial ryegrass cultivar used for the calibration and validation experiments of the AquaCrop model was Bestfor Plus, the most widely grown variety in the high tropics of Colombia. A seeding rate of 50 kg ha−1 was used. A total of 6.6 kg of seeds were distributed uniformly by hand over 1440 m2. After sowing, irrigation was carried out in order to ensure uniform soil moisture throughout the experimental area and to facilitate seed germination. A compound fertilizer, such as NPK (15-15-15) and magnesium sulphate, was used.
In both growing seasons, the experiment was laid out in randomized complete blocks with six irrigation regimes and eight replications. The irrigation regimes included full-irrigation (irrigation based on 100% field capacity (FC)), mild water stress (60% FC), moderate water stress (50% FC), severe water stress (40% FC), most severe water stress (20% FC) and non-irrigated (<20% FC). The irrigation regimes were applied using a linear source sprinkler irrigation system that allowed long-term evaluation of crop yield under continuous irrigation gradients, from over-irrigation to no irrigation [
29,
30]. The irrigation depth rate was 13.49 mm h
−1 lower than the basic infiltration rate of 21.6 mm h
−1, to avoid surface water ponding and runoff; thus, the irrigation system design was suitable for the soil type. The distribution uniformity was 86%, while the distribution uniformity of the lateral whole was 83.52%. The Christiansen uniformity coefficient was 89.59%, and the irrigation efficiency was 68.6%. The sprinklers used were the Toro Irrigation brand, model S-II, with an operating pressure of 249.76 kPa (36.25 psi). However, according to the guidelines specified by Hsiao et al. [
31] for the calibration, the “full irrigation” level was used for guaranteeing that the crop was evaluated at the maximum levels of performance and was validated with the “non-irrigated” level, which presents the most adverse conditions for the development of the crop.
The irrigation treatments used for calibration and validation of the AquaCrop model were identified as follows: C1-Irrigation: full irrigation treatment in the first cropping season of ryegrass (December 2008 to February 2010); C1-Non-Irrigated: non-irrigated treatment in the first cropping season of ryegrass (December 2008 to February 2010); C2-Irrigation: full irrigation treatment in the second cropping season of ryegrass (February 2010 to October 2010); C2-Non-Irrigated: non-irrigated treatment in the second cropping season of ryegrass (February 2010 to October 2010).
Soil moisture was measured every two days at a depth ranging from 0 to 30 cm, using the thermogravimetric method and TDR equipment. The water balance was obtained to determine evapotranspiration, assuming negligible surface runoff and evaluating deep percolation, defined as the water above the FC point under the roots. Actual evapotranspiration per experimental unit was determined by obtaining K
T, Ke, and Kc using the Penman-Monteith method [
32].
2.4. Phenological Data of the Ryegrass Crop (Lolium perenne L.)
Phenological data in calendar days and thermal time—growing degree days (GDD)—were obtained after field monitoring of the ryegrass crop; the main growth stages were defined, and early canopy senescence was not considered because Lolium perenne does not reach that stage. Degree days were calculated following the methodology described in the AquaCrop reference manual [
21]. The AquaCrop model uses thermal time to determine green canopy cover and is crucial for crop development. Crop phenology data are shown in
Table 1, divided into calendar days and degree days (thermal time) required to reach maximum canopy cover, flowering, and harvest index of accumulated length. The average time to emergence was 9 days with 83.6 °C day on average and a variation from 83 to 91 °C per day, considering the two crops grown.
2.5. Data Collection for the AquaCrop Model
2.5.1. Climate Data
During the two growing seasons (2008–2010 and 2010) the climate data required as inputs in the AquaCrop model were collected. The minimum climate variables required for AquaCrop include daily, decadal, or monthly minimum and maximum air temperature, solar radiation, relative humidity, wind velocity, reference evapotranspiration (ET
0), and precipitation. Daily meteorological data were obtained from a meteorological station, located at the experimental site, which is part of the network of meteorological stations of the Institute of Hydrology, Meteorology, and Environmental Studies (IDEAM) of Colombia. Reference evapotranspiration was calculated following the modified Penman-Monteith equation [
32] using ET
0 Calculator FAO version 3.2 [
33]. A default file of the annual mean CO
2 concentration measured at the Mauna Loa Observatory in Hawaii provided by AquaCrop was used.
Figure 1 shows the meteorological air temperature, reference evapotranspiration (ET
0), precipitation, and relative humidity on a daily basis during the two seasons or experimental cycles. The first season (2008–2010) consisted of a normal year, with 624 mm (5% below the historical average); in contrast, precipitation during the 2010 season was 1054 mm (61% above the historical annual average). During this period, Colombia experienced a strong cold phase of El Niño Southern Oscillation (ENSO) known as “La Niña”. This event was one of the most intense on record, both in duration and magnitude. From July 2010, positive anomalies were consolidated, which initiated the cold event and lasted 18 months, until December 2011 [
34].
Regarding reference evapotranspiration, which is the main input climate component in the AquaCrop model, the temporal pattern of ET0 is representative of the Colombian high tropics, with an average annual accumulated ET0 of 890 mm. The lowest ET0 values occurred during November and December (2.7 mm day −1) and the highest values occurred during September and October (5.2 mm day −1).
2.5.2. Soil Data
Unaltered soil samples were taken to determine the moisture retention curves. Based on these results, the usable water table and hydrodynamic soil levels such as Permanent Wilt Point (PWP) and Field Capacity (FC), Saturation Point (Sat) and Hydraulic Conductivity, as well as bulk density (Da) were calculated. FC and PWP were determined via the thermo-gravimetric method; we verified using the indicator plant method for sunflower (
Helianthus annuus) [
35]. The creation of the soil file in AquaCrop (SOL) required soil hydraulic parameters (
Table 2). The soil was classified as silty loam, with 31.2% sand, 50.0% silt, and 18.8% clay. The effective depth of the root zone was 0.3 m, the field capacity (FC) was 138.48 mm, the PWP was 90.02 mm, saturation (Sat) was 180.03 mm, the saturated hydraulic conductivity (Ks) was 226.45 mm day
−1, and the average soil bulk density was 0.85 g cm
−3. The soil of the sites is classified as Pachic Haplusstands–Humic Haplusstands–Fluventic Dystrustepts with symbols RMQa and RMQb [
36]. Soil chemical properties at the experimental site were evaluated at 0.00–0.20 m depths; the chemical properties are shown in
Table 3.
2.5.3. Crop Data
Growth was monitored daily from emergence to the end of each growing season;
Lolium perenne grassland was subjected to zero grazing throughout the experiment. During the productive phase, seven cuts were made in the first growing season and four cuts in the second evaluated growing season. To determine the constant dry weight and total dry matter (t ha
−1), in each season, harvests were made by cutting the forage present within an area of 0.5 m × 0.5 m (0.25 m
2) with three replicates at 7 cm of height above the ground. Cutting height is a major determinant of quantity and quality of stubble from which the sward will regrow in perennial glasses [
37]. From each green forage sample, a subsample of 500 g was taken and placed in paper bags in a drying oven at a temperature of 60 °C for 72 h. All samples were weighed with a precision scale (0.001 g) to determine the fresh and dry weight.
Table 4 shows an overview of the mean dry matter biomass weights observed for each cutting, plant height, and water supply condition.
Canopy cover was obtained from photographs taken at 1.4 m from the ground with a digital camera. The image was processed in CobCal v2.1 software [
38], where the user marks the colors of the pixels corresponding to the vegetation cover as positive pixels and the colors corresponding to the ground as negative pixels. Subsequently, the pixels are sorted by Euclidean distance, and the percentage of cover is calculated by counting the number of pixels corresponding to each group.
The AquaCrop crop files were created based on field observations of crop development and phenology. The AquaCrop model uses conservative and non-conservative parameters for the simulation. Conservative parameters do not change with location, management, cultivars, and time [
39]. Conservative parameters must be adjusted to improve the simulations in the model [
40]. They include canopy cover (CC), canopy growth coefficient (CGC), canopy decline coefficient (CDC), crop coefficient for transpiration at full CC, and normalized water productivity (WP*) for biomass formation. Crop water stress parameters (soil water depletion thresholds for leaf growth inhibition and stomatal conductance and for acceleration of canopy senescence) were taken from Terán-Chaves et al. [
41]. The crop parameters were iteratively adjusted with the help of the Independent Parameter Estimation Model (PEST) Ver. 5. [
42] (PEST is an acronym for ESTimation of Parameter) until a close match between measured and simulated parameters was achieved.
Water productivity (WP) for biomass production was determined as the ratio of biomass to actual accumulate transpiration [
43]. The initial value of WP* was obtained as the slope of the linear regression of a plot of biomass accumulation versus accumulated transpiration values normalized to ET
0, i.e., ∑Tr/ET
0.
2.6. Model Calibration and Validation
AquaCrop version 7.0 (2022) [
44] was used; the model was run in calendar days, and the perennial herbaceous forage crop file of alfalfa was taken as a reference. The standard window version 7.0 user interface included a database of perennial herbaceous forage crops, with multiple harvests, the amount of biomass, and crop yield harvested at each cut during the growing cycle in case of multiple cuttings; these data were stored in a ‘harvests’ output file. In this study, the calibration and validation guidelines described by Hsiao et al. were followed [
31]; data from the non-limiting soil water regime treatment (C1-Irrigation: full irrigation treatment in the first cropping season of ryegrass) were used to calibrate AquaCrop. The calibration process was performed by running the model with the specific input information of weather conditions, soil characteristics, field managements practice, and crop parameters. The calibration also involved adjusting the non-conservative parameters, including initial canopy cover CCo (%), maximum canopy cover (CCx), time from sowing to start of senescence (day), and maximum effective rooting depth (m), until a close match between observed and simulated biomass was obtained.
For the first stage, from sowing to first cutting, the soil surface cover of an individual seed at 90% emergence observed in the field and the final yield at the time of cutting were taken into account. For cuts after the first cut, the canopy cover after cutting (CCini) was specified at a value of 40% according to field measurements.
Once the model was successfully calibrated, it was validated using three independent datasets obtained from the experiment, namely C1-Non-Irrigated: non-irrigated treatment in the first cropping season of ryegrass (December 2008 to January 2010), C2-Irrigation: full irrigation treatment in the second cropping season of ryegrass (February 2010 to October 2010), and C2-Non-Irrigated: non-irrigated treatment in the second cropping season of ryegrass (February 2010 to October 2010).
2.7. Model Evaluation Statistics
The goodness-of-fit of the AquaCrop model for ryegrass was evaluated using the following five statistics: the coefficient of determination (R2), the Willmott index of agreement (d-index), the root mean square error (RMSE), the normalized root mean square error (NRMSE), and the Nash-Sutcliffe model efficiency coefficient (EF). The evaluations of simulation results were recorded in statistics output files. The output files contain the statistics of the evaluation of the simulation results for canopy cover, biomass, and soil water content.
According to FAO [
45] for R
2, (Equation (3)) values > 0.90 were considered to be very good, while values between 0.70 and 0.90 were considered to be good. Values between 0.50 and 0.70 were considered to be moderately good, while values below 0.50 were considered to be poor. The d-index (Equation (4)) ranges from 0 to 1, where 0 indicates no agreement and 1 indicates perfect agreement between simulated and observed data; the d-index was acceptable when it was above 0.64. RMSE (Equation (5)) varies from 0 to positive infinity and is expressed in units of the studied variable. An RMSE close to 0 indicates good model performance. The NRMSE (Equation (6)), on the other hand, gives an indication of the relative difference between the simulated and observed values. NRMSE < 5% is considered very good; 6~15% is good; 16~25% is moderately good, 16~25% is moderately poor, and NRMSE > 26% is poor [
46]. The efficiency coefficient of the Nash–Sutcliffe (EF) model (Equation (7)) determines the relative magnitude of the residual variance, compared to the variance of the observations. An EF indicates how good the fit of the plot of observed vs. simulated data is on the 1:1 line; it ranges from minus infinity to one. One means a perfect fit, and zero indicates that the model predictions are as accurate as the average of the observed data and negative when the mean of the observations is less than the model predictions. An EF less than 0.4 is considered deficient. The simulation results were considered good when at least three of the five statistical fit indicators of the model evaluation were classified as good to very good.
where
= is the observed data;
is the average of observed data;
is the simulated data;
is the average of simulated data; and
n is the observation number.
4. Discussion
To date, forage grass models have been developed to simulate perennial ryegrass growth processes under temperate climates [
49,
50]; hence, they cannot be used for predicting grassland productivity in tropical regions such as Colombia. This study is, to our knowledge, the first to calibrate and validate the AquaCrop model for perennial ryegrass (
Lolium perenne L.) using version 7.0.
The results showed that the AquaCrop (v 7.0) model was able to simulate perennial ryegrass growth under normal and wet seasons in the high tropic of Colombia. This capacity may allow many future applications for tropical pasture species with high importance for livestock or the production of energy from biomass. However, the capacity of the AquaCrop model for simulating the effect of grazing on late regrowth pasture and its effects on canopy cover and biomass must be further studied.
The model simulated canopy cover growth well from first cut to fourth cut; however, after the fifth cut, a rapid decline in canopy cover was generated instead of the gradual decline rate observed in the field, which could be attributed to the indeterminate growth characteristic of perennial ryegrass. Previous studies have identified this limitation of the AquaCrop model in crops exhibiting indeterminate growth characteristics [
51,
52,
53]. AquaCrop does not consider leaf appearance rate or phyllochron; this may explain the underestimation of the simulated values. The potential growth rate of the leaf area is proportional to the product of tiller density, the number of elongated leaves per tiller, a constant leaf width, and a temperature dependent rate of leaf elongation [
11]. Most plant processes are interrupted during days when a cutting takes place; in the AquaCrop model as is in the BASGRA model, all leaf area associated with non-elongating tillers above a threshold is removed by cutting, as is the associated biomass; this also affects the development of the remaining canopy cover after the cuts.
The AquaCrop model was able to simulate biomass with acceptable accuracy under both irrigation practices, but the simulated results were observed to be slightly better suited to full irrigation practices. Full irrigation practices compensate for any lack of water from precipitation, which enables the model to quantify results with reasonable certainty.
Grazing reduces the development and growth of ryegrass reproductive tillers [
54], which complicates the effects of reproductive growth on herbage accumulation, especially for late regrowth, which AquaCrop is possibly trying to simulate. To increase the accuracy of the model, the effect of grazing on the growth and development of reproductive tillers needs to be incorporated, along with a more detailed simulation of plant management and phenology. The variation of pasture growth in response to irrigation was also predicted. This evaluation provided confidence in the model’s ability to simulate pasture herbage accumulation in the annual season and under various management scenarios and a wide range of pasture environments.
The importance of soil moisture deficits for ryegrass persistence was demonstrated in a modeling study by Woodward et al. [
49]; soil water is important for agricultural production and is a key parameter in hydrologic models and weather prediction models. We found that AquaCrop can estimate soil moisture with acceptable precision. Soil water content was reasonably simulated, albeit simulated values had a tendency for greater variability compared with observed values. Perennial ryegrass is moderate to poorly adapted to low soil moisture availability [
50]. Water shortage limits leaf appearance, leaf expansion, and tiller initiation, irrespective of the availability of other resources, and largely explains inter-annual variability in pasture growth rate [
55]. Future studies should explore the sensitivity of our results to a much wider range of soil profile and available water.
5. Conclusions
The results obtained in this study show that AquaCrop is adequate in simulating the responses of perennial herbaceous forage crops to different water regimes; however, the goodness-of-fit evaluation of AquaCrop v 7.0 for crops with multiple harvests during a single season should be generated for each harvest or cutting and not as a cumulative biomass value as is currently presented.
Additional experiments are needed to adjust the parameters developed in this study to account for other environmental conditions and to properly estimate biomass per cutting. In the meantime, this study serves as a baseline for further modeling of perennial herbaceous forage crops with AquaCrop version 7.0 and newer.
Future modeling studies of perennial herbaceous forage crops should delve further into the comparison of soil moisture content simulations under various irrigation practices and climatic conditions. In addition, further experimentation with indeterminate crops such as ryegrass are needed to characterize a possible enveloping senescence curve, crop recovery beyond the permanent wilting point, and early canopy senescence processes due to natural causes.