Next Article in Journal
Identification and Differentiation of the Hierarchical Structure of the Caribbean Cruise Shipping Network Based on Route Organization
Next Article in Special Issue
Agroforestry for Sustainable Food Production
Previous Article in Journal
Forest Fire Susceptibility Assessment and Mapping Using Support Vector Regression and Adaptive Neuro-Fuzzy Inference System-Based Evolutionary Algorithms
Previous Article in Special Issue
Mainstreaming Smart Agroforestry for Social Forestry Implementation to Support Sustainable Development Goals in Indonesia: A Review
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Assessment of a Cocoa-Based Agroforestry System in the Southwest of Colombia

by
William Ballesteros-Possú
1,*,
Juan Carlos Valencia
2 and
Jorge Fernando Navia-Estrada
1
1
Department of Natural Resources and Agroforestry Systems, Universidad de Nariño, Ciudadela Universitaria Torobajo, San Juan de Pasto 52001, Colombia
2
Agricultural Sciences School, Universidad Abierta y a Distancia—UNAD, Tumaco 528509, Colombia
*
Author to whom correspondence should be addressed.
Sustainability 2022, 14(15), 9447; https://doi.org/10.3390/su14159447
Submission received: 8 June 2022 / Revised: 22 July 2022 / Accepted: 25 July 2022 / Published: 2 August 2022
(This article belongs to the Special Issue Agroforestry and Sustainable Agricultural Production)

Abstract

:
Cocoa-based agroforests play an important role in farmer livelihood and the global environment; however, despite these facts, their low yields and tree aging put at risk their fate. This project investigated the carbon storage potential, productivity, and economics of different agroforestry arrangements of cocoa (Theobroma cacao) with Melina (Gmelina arborea) trees, in the southwest of Colombia. We established the experiment under a Randomized Complete Blocks design with seven treatments and three repetitions. Different allometric models were tested. Allometric models were made for G. arborea trees with dbh, ranging between 30.24 and 50.11 cm. The total carbon accumulation fluctuated between 49.2 (Treatment 4) and 88.5 t ha−1 (Treatment 2), soil organic matter (SOM) ranged between 9 and 17%, bulk density decreased from 0.83 to 0.77 g cm−3. Cocoa yield ranged between 311 kg ha−1 year−1 (Treatment 7, traditional farm) and 922 kg ha−1 year−1 (Treatment 6). Treatment 6 showed the best performance with a net present value (NPV) of COP 1,446,467 (US $337.6), an internal rate of return (IRR) of 42%, and a cost-benefit ratio (B/C) of 1.67%. The benefits of AFS were also evidenced in some of the physical and chemical soil properties. Despite local marginality, these cocoa agroforest arrangements are a viable alternative to improve the traditional (local) cocoa systems because cacao agroforest arrangements increased cacao yield and carbon storage becoming a suitable alternative to improve traditional systems.

1. Introduction

Food security and climate change represent one of the most worrisome threats to the global environment and humanity due to the impacts caused on human health, biodiversity, food security, economy, natural resources, and infrastructure [1]. These troubles will significantly threaten human fate because of their social, environmental, and economic impacts and the high cost of implementing adaptation and mitigation measures [2]. Therefore, the 2030 agenda for ‘Sustainable Development members’ calls attention to protecting the planet from degradation and taking urgent action to tackle climate change concerns [3].
Fortunately, many of these hazards can be reduced by increasing resilience and resource-efficient use in agricultural production systems [4], which will improve the local farmers’ adaptive capacity. Similarly, the FAO proposed a ‘climate-smart agriculture’ (CSA) approach, a tool to improve agricultural productivity and reduce yield variability over time under adverse climatic scenarios [4,5].
GHGs could be mitigated in two ways: by reducing anthropogenic CO2 emissions or by creating and improving carbon sequestration sinks [6]. Agroforestry systems (AFS) and the mixture of crops and trees are a C sink and an alternative to mitigate the effect of the agricultural production systems [7] because they integrate agricultural landscapes with rural communities [8]. AFS, the art and science of farming with trees [9,10], is a multifunctional land-use system that offers environmental services in agricultural landscapes [9,11]. For instance, cacao agroforests preserve the natural soil biota, control soil erosion, and provide sustained land use land while maintaining suitable yields [12,13,14].
These systems can sequester and store atmospheric carbon, in agricultural lands at a low cost [7,8]. Growing windbreaks, shelterbelts, silvopastoral systems, forest farms, riparian buffers, woodlots, promoting natural regeneration of vegetation, and the conservation of forests make an enormous contribution to the local carbon budgets [11,12,13,14,15,16,17,18].
Trees in the AFS also provide numerous goods and environmental services that benefit farmers, landscapes, and infrastructure and reduce the susceptibility to extreme climatic events, making it a tool for Smart agriculture approaches [18,19,20,21,22,23]. Likewise, Agroforestry is considered a sustainable and efficient land management system, the AFS can contribute to the implementation of 9 out of the 17 SDGs, and special attention is paid to food security, climate change adaptation and mitigation, and biodiversity [24].
Environmentally sustainable practices are one of the highest priorities for agricultural systems in the tropics [25,26]. An overview of the main technologies currently used by cocoa growers, in Colombia, shows that cocoa growth under traditional production systems [27,28], with low technology, old cacao trees, and high shading. These conditions trigger fungal diseases such as frosty pod rot (Moniliophthora roreri) and Witch’s broom (Moniliophthora perniciosa) [29], which reduce substantially cocoa yields. In this scenario, traditional farms average a yield of 300 kg ha/year [27,30]. The outcome of various researchers conclude that these systems are not viable for cocoa farmers [16]; however, other researchers identify important social and economic co-benefits of environmentally-friendly cocoa production regarding reduced pesticide use, resource conservation, long-term productivity, soil health, and human welfare [31].
On the other hand, cocoa farming, however, is associated with numerous environmental, social, and economic concerns, such as deforestation, child labor, and farmers’ poverty [31], that lead to public and consumer pressure [32] and a growing claim for sustainably-produced cocoa [33]. Thus, cocoa traders and chocolate companies have started addressing farm-level sustainability through supply chain mechanisms [34].
Past research on cocoa sustainability has mostly focused only on child labor in the value cocoa chain [35], environmental impacts, and the relationship between environmentally-friendly farming practices and profitability [36].
Full-sun cocoa farming is currently the most widespread cocoa cultivation system in the world [37]; however, its negative effects including biodiversity loss, soil fertility depletion, and soil quality degradation, have incredibly received low attention. Some ecofriendly purposes must be studied to revert the ecological effects of full-sun cocoa systems.
T. cacao-G. arborea association has been little studied on the pacific coast of Colombia despite its good performance; thus, a better understanding of its economic and environmental effects is required [30], to offer different strategies to cocoa farmers’ decision makers about the new cocoa production systems in the country.
The potential of AFS to store aboveground carbon is estimated to be 1.9 × 109 Mg C year−1 intemperate, and 2.1 × 109 Mg C year−1 in tropical biomes [38]. Carbon accumulation in monoculture of trees and crops shows 40% and 84% less than AFS, demonstrating that AFS is an important carbon sink in agricultural lands [39,40,41].
This research is focused on answering what are the carbon storage potential and profitability of different cocoa-based agroforestry arrangements compared to traditional cocoa systems? Therefore, the purpose of this research is to assess cocoa-agroforestry arrangements’ potential to increase the yield and storage in atmospheric carbon compared to traditional cocoa systems. For that, understanding the agroforestry arrangements’ performance was important for adoption purposes taking into account the ‘view of the farmer’ which facilitates the implementation of improved agroforest arrangements [42].

2. Materials and Methods

2.1. Study Area

The research was carried out in Tumaco, Nariño, southwest of Colombia, located at 01°39′12′′ north latitude and 78°41′49′′ west longitude (Figure 1). The experimental zone, located in a Tropical Rain Forest (bh-T) [43] had an average temperature of 27 °C, relative humidity of 80%, precipitation of 2800 mm/year, and a solar brightness of 1008 h/year [44].
The agroforestry system was 10 years old, established under an experimental plot of four ha, with a Complete Randomized Blocks Design (CRBD), and encompassing three blocks and seven treatments. Each trial unit had 1600 m2. Table 1 gives more details about treatments. The G. arborea trees have a dbh range between 30.24 and 54.11 cm, and a height range between 57.03 cm and 27.61 m, respectively.

2.2. Tree Sampling

The tree sample size was 70 trees (35 of G. Melina and 35 of T. cocoa), five for treatment chosen randomly to replicate the whole range of diameters and height in the treatments. Tree biomass was attained according to McDicken, and Picard et al. approach [45,46].
We cut Melina trees (five for treatment) at ground level and immediately: (i) separated four fractions of aboveground biomass (i.e., stem, branches, twigs, and leaves); (ii) weighted each fraction (total fresh weight) using a hanging field-scale (Golden Lark model, precision 200 g), and (iii) collected a sample of 500 g from each fraction of aboveground biomass and stored each sample in a paper bag, which was subsequently weighed on a precision balance (Kern 440-55N, precision 0.2 g, Ebingen, Germany).
In the lab, the samples were dried at a temperature of 64 °C until they reached a constant weight. the moisture content of the sample was determined with Formula (1). These values were extrapolated to the biomass of different components of the cut trees; then, using the 0.47 conversion factor [47] biomass-carbon carbon stock was attained.
B i o m a s s = T o t a l   f r e s h   w e i g h t × D r y   w e i g h t   F r e s h   w e i g h t × 100

2.3. Data Processing

A total of 17 models were evaluated; eight equations were proposed by different authors (Table 2) and nine by the study authors. Some of these regression models included transformed data to estimate biomass based on trunk dbh and height. Although dbh is currently used for most local or regional biomass estimations, some researchers have suggested that both dbh and height should be included for larger-scale applications [48,49]. As such, we included height in some models for estimating biomass in these open-grown trees.
Before and after evaluating the best-fit model to the G. arborea biomass data, the homoscedasticity (constant variability of errors), normality errors, linear independence, and linearity of the residuals were tested. Homoscedasticity was accomplished by eliminating three observations (outliers) and applying the Breusch–Pagan test for constant variance. Normality was attained by using the QQ-plots and the normal curve, in this, some deviated points were observed in the tails, but they did not affect normality. Linear independence was found with Pearson’s correlation coefficient, which was not significant between explanatory variables. Finally, linearity was in some cases met using the exact valor of lambda [51] or log transforming response variables. A correction factor prevented us from bias in biomass prediction when log-transformed variables are used [52,53] (Equation (2)).
C F = exp ( S E E 2 2 )         o r         exp ( v a r i a n c e 2 )
where CF is the correction factor, SEE the standard error of regression estimate, and variance is the square of the root-mean-square error (RMSE2) in logarithmic form. Finally, the validation process consisted of two steps. First, the database was split into two parts, one for training, which corresponded to 80% of the data, and the other for testing, which retained the remaining 20%. Second, the final competing models were evaluated with the variance inflation factor (VIF), the R2, and the mean squared prediction error (MSPE) [54,55,56]. After selecting the best-fit equation, graphic analysis of the student residuals was performed to test for normality and heteroscedasticity in the errors.
On the other hand, cocoa aboveground biomass was calculated by using a regression equation [57] which is based on the tree collar diameter at 30 cm as given in Equation (3).
L o g A G B = 1.625 + 2.626 l o g   ( D 30 )
where AGB = Aboveground biomass; D30 = tree diameter at 30 cm aboveground.
Cocoa belowground biomass was attained with Equation (4) [58].
B G B = exp [ 1.0587 + 0.8836 L n ( A B )
where BGB = root biomass (t ha−1); Ln = natural logarithm; exp: power base e.
AB = Total aboveground biomass (t ha−1) of cocoa
Concerning cocoa yield, in all treatments, it was measured monthly.

2.4. Data Analysis

Tree carbon storage and cocoa yield were compared with the One-way ANOVA procedure and the adjusted Tukey test to detect differences among treatments. Data processing was carried out with SAS 9.3 and R 3.5.3. (R Core Team, Vienna, Austria) software [59].

2.5. Economic Analysis

Production cost and cocoa yield from each treatment was monthly registered, while G. arborea trees were valued in situ at USD 15.79. The economic analysis was performed on a hectare basis over the 10-year period using the Net Present Value (NPV) (5), the Internal Rate of Return (IRR) (6), and the Benefit-Cost Ratio (BCR) (7) indexes.
N P V = t = 1 n C F t ( 1 + r ) t C o
IRR   =   0   =   N P V = t = 1 n C F t ( 1 + r ) t C o
B C R =   P V   b e n e f i t s   P V   c o s t s  
where:
CFt = net cash inflow-outflows during period t
r = internal rate of return that could be earned in alternative investments
t = time period cash flow is received
n = number of individual cash flows
Co = Total initial investment cost
PV = Present value

3. Results

3.1. Carbon Storage Potential of Agroforestry Arrangements

The agroforestry system with cocoa showed statistical differences (Pr < 0.0001) for aboveground C stored by the agroforestry system (T. cocoa and G. arborea). The highest C for the stock arrangements was treatment 7 (14.02 t Cha−1 year−1), while for the improved arrangements, it was treatment 2 (11.32 t Cha−1 year−1) (Figure 2C). The outcomes of the other treatments ranged between 8.73 and 6.29 tCha−1 year−1; accordingly, the total carbon accounted (below- and aboveground) by the agroforestry systems in 10 years was between 140.226 and 62.85 tCha−1 (Figure 2D), which is equivalent to a 14.02 to 6.29 tCha−1 year−1.
G. arborea aboveground carbon had statistical differences (p < 0.0001) among treatments, treatment 2 displayed the highest amount of biomass stored with 5 t Cha−1 (Figure 2A). T. cacao aboveground biomass had statistical differences (p < 0.0001) among treatments too. Treatment 7 showed the highest potential (6.7 t Cha−1) (Figure 2B). The difference in carbon stored by traditional cocoa agroforest compared to improved arrangements was around 20%.

3.2. Biomass Allometric Equations

Comparing different allometric models using data from destructively sampled G. arborea trees, 15 models fitted the data rationally well, fulfilling almost all information criteria (Table 3).
According to the results in Table 3, models 1, 2, 4, 10, 13, 14, and 15 were selected. These had the highest determination coefficient, VIF less than 10, lowest Akaike information criteria (AIC); Bayesian information criteria (BIC); predicted residual sum of squares (PRESS); Mallows’ Cp (Cp); Variance inflation factor (VIF) and Furnival index (FI). These competing models were tested to determine their accuracy using mean square prediction error (MSPE) (Table 4). The best predictor model was Berkouth with MSPE = 5.74 which was very close to the ‘This study 3’ model.

3.3. Cocoa Yield

The variance analysis showed significant statistical differences (p > 0.0001) in cocoa yield by the treatments. Treatments 2, 3, 4, 5, 6 and 1 showed the highest yields (922, 845, 838, 837, 831, 710 kg ha−1) (Figure 3A); treatment 1 presented the lowest. When the improved cocoa arrangements were compared to traditional cocoa farms (treatment 7), the improved arrangements showed significant differences. The traditional cocoa farm had the lowest yield, with an average of 310.67 kg ha−1 year−1.
There was also a positive effect of all AFS in reducing soil bulk density (Figure 3B) where there were no significant differences in the treatments within the blocks, but between the three blocks studied, there was a reduction. This reduction was equivalent to an average of 23%. These results show that the AFS is an alternative for improving soil health.
In the soil organic matter (SOM), there were no significant differences in the treatments within the blocks but between the three blocks studied there was an increase (approx. 17%) in the amount of organic matter transferred by the AFS to the soil (Figure 3C).

3.4. Economic Analysis

The economic analysis shows that all treatments had positive values in the indicators analyzed (Table 5). Compared to all improved cocoa arrangements, treatment 6 offers the best profitability with an NPV of 1446.45 (Colombian pesos—$ COP), an IRR of 42%, and a BCR of 1.67. The lowest performance treatment was treatment 2 with an NPV of 1262, an IRR of 25%, and a BCR of 1.16. Relating these values with those obtained by the cocoa traditional farm (treatment 7), the traditional farm displayed even lower values in these indices (NPV 651.65, IRR 13%, and a BCR of 1.02).

4. Discussions

4.1. Carbon Stored by the AFS

The carbon capture and storage potential depend on the agroforestry framework’s structure and functions dictated by various socio-economic and environmental factors [60]. In this study, total biomass (aboveground and belowground) in all treatments was lower than the control (traditional coca farm). The conceivable explanation behind this could be the effect of microclimatic interactions in cocoa-based agroforestry systems, the spacing [61], the age/diameter, and the miscellaneous structure of traditional farms. It is reported that radiant energy and rainfall interception by foliage and the temperature and humidity of the air surrounding the foliage [62] impact plant growth. This study detected that treatments with fewer woody trees and cocoa (traditional farm) but with multiple understory species growing with them stored more biomass. In the same way, the traditional cocoa agroforest was older than all modern cocoa arrangements, which affected the carbon storage budget. Despite cocoa’s high-density planting (HDP) being reported to reach higher cocoa yield than traditional ones (less than 700 trees/ha) [63], its effects on carbon storage are limited [64].
Many authors report the potential of C storage by G. arborea. For example, total biomass C stocks (above- and belowground) increased five-fold from the monoculture to the multi-shade tree system (from 11 to 57 Mg ha−1), this increase was associated with a six-fold increase in aboveground biomass, but only a 3.5-fold increase in root biomass, indicating a clear shift in C allocation to aboveground tree organs with increasing shade for both cacao and shade trees [65].
G arborea plantation stored 41.6 t C ha−1 at one year and three months old, in Costa Rica [66]; 22.9 t C ha−1 at six years, 145.4 t C ha−1 at nine years old in Madhya Pradesh, India [67], 8.31 t ha−1 at 3 years old in Mexico [61], 15.54 t ha−1 at four-year-old, in Mexico [68], 24.39 t ha−1 at six years old in Colombia and [69], 41.6 t ha−1 all five years old [70]. The C storage potential from these outcomes ranges from 2.77 to 40 t C ha−1, reflecting the effect of environment, site index, and spacing on the C stored by G. arborea. Therefore, the range from 16.2 to 20.9 t ha−1 yr−1 [71] does not encompass the total variability of the G. melina in different scenarios.
T. cacao carbon storage potential in AFS seems to be in the range of agroforestry systems. For instance, a 13-year-old gmelina-cacao agroforestry system stored 185 Mg C/ha in the Philippines [72], which is lower than a pure gmelina plantation (294 Mg/ha). This could be due to the spacing because it favored the development of cacao trees. However, we found that in the opposite case, the trees of treatment 1, despite having the highest planting density (1111 trees ha−1), reported the lowest C storage with a potential of 2.36 t tCha−1 year−1. One reason is that possibly the high humidity and the low luminosity in the tropical forest increased by the planting density caused more longitudinal growth than that in diameter, generating more foliage than wood. The average C storage potential ranging from 1.7 to 3.3 t tCha−1 year−1 [73,74] is lower than in this study.
Cocoa planted in very shady environments leads to lower rates of CO2 assimilation and lower production of fruits and biomass. Regarding water availability, there are already reports that cocoa plants adjust their physiology [74]. Therefore, light and water are one of the factors that can favor or stress cocoa plants, becoming an important factor in plant growth and photosynthetic rate [75].
The high carbon stored in this study could partly be explained by the fast-growth tree rate and the high stand density in some of the AFS. Furthermore, site conditions in the study area support optimum growth for G. arborea and T. cacao. Therefore, it appears that the high nutrient requirement of G. arborea [76] is adequately met by the soils of the study area. This is to be expected since they were planted on humid tropical rainforest soils where biomass production is higher, and it is associated with soils with pH > 6 and C:N ratio > 20 [71]. Thus, soil organic matter is an important indicator of agricultural productivity and environmental resilience and is vital for soil structure stabilization, improvement of water-holding capacity, and retention of crucial plant nutrients [1].
The introduction of trees improves the potential of agricultural lands to store soil organic carbon [9,77,78,79,80]. Numerous authors report greater stocks of carbon in agroforestry than in field crops [9,81].
The values for bulk density found in this study corroborate the positive effects of AFS on soils. These values represent an improvement in the soil quality over the first 20 cm, which is very important to understory plants [22].

4.2. Allometric Models

We tested and proposed linear regression models of the square root, logarithm, and power of the biomass using coefficients extracted from tropical AFS biomass data. Our optimal models have only dbh as the independent variable, which met all statistical parameters [54]. Tree height was left out because of its effect on multicollinearity [54]. The models explain more than 90% of the sample’s variance with MSPE lower than 7%. These results are within the range of those reported by similar studies in AFS [11,81]. The response variable without transformation got the best accuracy in biomass prediction. However, the power regression function (formula as: y = a × exp(b × dbh)) had a prediction accuracy very close to untransformed data.
Logarithmic allometric models are used in tree biomass studies [79]; in this research, log-transformed model fitted the data well but with lower R2. The advantage of these models is that they can be derived by linear regression and be generalized more easily than linear or weighted regression models [79]. Their disadvantage is that the sum of component estimation usually does not equal estimates from real data and has to be adjusted when the response variable is log-transformed. In this case, the correction factor was 1.032. In some cases, logarithmic transformation of the dependent variables stabilizes the variance and fits well with the model meeting the information indexes’ requirements [80,81].
The initial observation was that all the models generated in this study met accuracy criteria, having low AIC, BIC, PRESS, IF, IV, and very high R2 (Table 3). It indicates the independent variable (dbh or dbh-height) explained a very well high proportion of the variation in C.
Generic models met most of the information criteria. Unfortunately, when they were tested for variance inflation (VIF) and R2 indexes, some failed. High VIF values greater than 10 suggest that the predictor variables considered in a regression model are highly correlated with themselves and are synonymous with multicollinearity [80].
The allometric models showed a similar prediction of the total aboveground biomass with some models [81] but disagreed with others [41,82], which over- or underestimated the total aboveground biomass for trees with higher dbh. These outcomes call attention to reviewing the background of each model before using it. The two winner models performed the best in the validation process (Table 4), but some warning must be taken when using them. In this regard, before using any allometric model, it must be ensured that the data are within the validity range of the selected models [41].
From this call, it can be inferred that the derived allometric models can be correctly and efficiently used to estimate the aboveground biomass and carbon stocks in AFS. To sum up, there is an attractive opportunity for farmers to benefit financially from traditional and AFS with G. arborea if the cocoa growers can access the carbon markets because these arrangements had a high potential to produce environmental services.

4.3. Cocoa Yield in the Agroforestry Arrangements

The agroforestry arrangements evaluated showed variability in cocoa yield. The high planting densities (lower spacing) increased humidity triggering cocoa diseases and demanding high labor to control them [23,27]. The low yields of the traditional farm (treatment 7) indicate that traditional cocoa farms are not profitable if their only objective is cocoa yield [23,27]. However, if evaluated as a system, including all good and environmental services such as biodiversity, the results may differ. In this sense, some cacao growers state that the institutional trend to increase cacao planting densities goes against the traditional farmers’ view because the low cocoa trees’ density (400 trees ha−1) allows them growth miscellaneous crops for their livelihood [23]. However, with some new practices, they can increase their yield to 1000 kg ha−1 keeping these traditional cocoa arrangements [83,84].
In the traditional system, the energy investment is less than commercial ones; for every 1 megajoule invested, 23 are produced (1:23 ratio) [27]. Therefore, the energy balance is highly efficient. On average, cacao yields were, 41% higher in monocultures, but the revenues derived from traditional cocoa agroforest economically overcompensated for this difference. Indeed, the return on labor across the years was roughly twice higher in the agroforestry systems than in the monocultures [84].
When analyzing yield in each of the treatments, the same trend can be observed with the traditional farm reporting the lowest values. However, in the dry season, which occurred in the municipality between July to October, there was a slight separation of the treatments, suggesting that the shading produced a differential effect.
For good performance and yield of cocoa-based systems, the companion trees should provide a shade below 50%; the most recommended is 30% [85] because shade greater than 60% causes yield limitations [86,87]. However, cacao has been traditionally grown under shade regardless of yield [86]. In an experiment in Ghana, strong reductions in yield were observed due to shading. Cacao trees growing in full sunlight had a higher yield than the shading ones [87]. Conversely, scientists and environmentalists alike are beginning to realize this switch’s error for the ecology of cocoa plantations [88]. Canopy cover-up to 39% raised yields at the field level compared to cacao grown in full sun, but increasing shade above this level can limit yields [89,90]. Whereas in Cameroon, increasing canopy cover-up to 47% enhanced yield but greater than 60% reduced cocoa yield [91].
Therefore, growing in sunlight will require more intensive management, including increased fertilizer inputs [85]. Shading may not be required in all cacao-farm regions, its applicability is dependent on local climate conditions. That is why the control of both the growth and density of cacao trees, the increases in aeration, light perception, and fertilization [88,92] are necessary to raise the yield.

4.4. Economic Assessment of the Agroforestry Arrangements

The low profitability of the traditional cocoa agroforests agrees with most studies [93]. They indicate that traditional cocoa-based AFS with few forest species, and few investments generate low incomes. However, lower yields, in some cases, can be offset by cacao’s premium prices [94]. This is an important finding because traditional/indigenous production systems make a high contribution to the environment and rural welfare, more economic research is needed. In other scenarios, the revenues derived from agroforestry by-crops, economically overcompensate due to self-consumption of companion crops, such as bananas, fruits, herbs, and peach palm, among others [94,95]. There is a bias, when assessing cacao production systems because most studies focus on cacao yields without quantitatively evaluating the economic returns from companion crops [86]. Other drawbacks of the cacao farms’ competitiveness are a lack of access to the market and low density of trees (400 per ha). Therefore, despite their potential to increase farmers’ revenues, crop products have been mainly used for self-consumption [96].
Results show that cacao yields were, on average, 41% higher in improved cacao agroforestry, but the revenues from agroforestry companion crops have great potential. The explanation about high IRR in treatment 6 could be the result of the optimum performance of G. arborea trees under these spacing and alley arrangements and that G. arborea is a sunlight-demanding, drought-resistant tree, which has fairly good tolerance to moist soils [97]. Under these conditions on the Colombian pacific coast, G. arborea trees reached dbh and heights higher than 50 cm and 11 m, respectively, which were sold at $70.000 COP, (USD 17.5). Indeed, the best economic performance was attained with intermediate diversity (three to seven species) and a density of 100 to 400 companion plants ha−1) [98]. The same trend was reported in another study where G. arborea agroforest was 2–3 times more profitable in terms of net present value compared to sole G. arborea or mango or pigeon pea [99], these tendencies are very close to the results in this study. When comparing the cost of all improved cocoa arrangements they had no significant differences; however, when compared to traditional systems the differences were outstanding. Traditional agroforestry budgets are very low (1 million COP, USD 250, approximately), especially for labor, which allows farmers to develop miscellaneous activities and the use of on-farm inputs. Sustainable production systems such as agroforestry and organically managed systems are expected to yield less cacao but by-crops and premium prices, respectively, might economically compensate for the lower yields [84].
The IRR of 41% was high compared to the banks’ discount rate but there is no information about the IRR for other agricultural systems in the region.
These findings provide a roadmap for optimizing crop diversity and density to adjust the economic balance between sales and self-consumption in cocoa AFS.
Finally, if agroforestry is to be used in carbon capture and storage schemes such as the clean development mechanisms, better information is required to determine above- and belowground carbon stocks and soil carbon in agroforestry systems landscapes [100]. Thus, there is a need for biomass estimation, which is sensitive to a specific arrangement, objectives, spacing, companion plants, and management practices. The AFS assessed in this study could be a good alternative for the Colombian government to full fill its commitments to COP 21 and the Sustainable Development Goals– SDG [100], or the 2030 agenda in SDG 13 (climate action) [101].
Further research is needed to investigate the impact of different ways of integrating miscellaneous trees with cocoa on wider environmental, social and economic sustainability aspects, that are driving increasing interest in the SDGs, climate change, and food security [102,103,104]. Likewise, it is needed to design the strategies for adopting [105] these results in the region.

5. Conclusions

The carbon stock in the different agroforestry arrangements was statistically different. The lowest accumulation happened in treatment 4 and the highest in treatment 2. To estimate the biomass produced in the different agroforestry arrangements, two allometric models were developed for G. arborea based on dbh. Cocoa yield showed significant statistical differences in the different arrangements. The proposed agroforestry arrangements had positive effects on soil bulk density (Da) and organic matter, the first was reduced and the second had a significant increase. All agroforestry arrangements had positive financial benefits. Overall, treatment 6 presented the best performance in all financial indexes.

Author Contributions

Conceptualization, W.B.-P. and J.C.V.; methodology, W.B.-P., J.C.V. and J.F.N.-E.; software, W.B.-P.; validation, W.B.-P., J.C.V. and J.F.N.-E.; formal analysis, W.B.-P.; investigation, W.B.-P., J.C.V. and J.F.N.-E.; resources, J.F.N.-E.; data curation, W.B.-P.; writing—original draft preparation, J.C.V.; writing—review and editing, W.B.-P. and J.F.N.-E.; visualization, J.F.N.-E. and J.C.V.; supervision, J.F.N.-E.; project administration, W.B.-P.; funding acquisition, J.F.N.-E. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Project ‘Fondo Colombiano de Ciencia Tecnología e Innovación-FCTI del Sistema General de Regalías, grant number BEPIN 2015000100001’ and ‘The APC was funded by MDPI discount vouchers’.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Acknowledgments

We would like to thank all the people who collaborated in this study: mainly the farmers of the Rescate las Varas Village, and the countless people who cooperated selflessly in the fieldwork, including the Cortepaz cocoa growers’ association.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Wheeler, T.; von Braun, J. Climate change impacts on global food security. Science 2013, 341, 508. [Google Scholar] [CrossRef] [PubMed]
  2. IPCC. Climate Change: Synthesis Report. Contribution of Working Groups I.; II and III to the Fifth Assessment Report of the Intergovernmental Panel on Climate, Change; Core Writing Team, Pachauri, R.K., Meyer, L.A., Eds.; IPCC: Geneva, Switzerland, 2014; 151p. [Google Scholar]
  3. United Nations Organization—UNO. Sustainable Development Goals. Available online: https://www.un.org/sustainabledevelopment/sustainable-development-goals/ (accessed on 23 January 2021).
  4. Lipper, L.; Thornton, P.; Campbell, B.; Baedeker, T.; Braimoh, A.; Bwalya, M.; Caron, P.; Cattaneo, A.; Garrity, D.; Henry, K.; et al. Climate-smart agriculture for food security. Nat. Clim. Chang. 2014, 4, 1068–1072. [Google Scholar] [CrossRef]
  5. FAO. Climate-Smart Agriculture Case Studies. Successful Approaches from Different Regions; FAO: Rome, Italy, 2018; 44p. [Google Scholar]
  6. Anguiano, J.M.; Aguirre, J.; y Palma, J.M. Cunnigham y Pennisetum purpureum. Cuba CT—115. Av. Investig. Agropecu.-Aia 2013, 17, 149–160. [Google Scholar]
  7. Udawatta, R.P.; Jose, S. Carbon sequestration potential of agroforestry practices in temperate North America. In Carbon Sequestration Potential of Agroforestry Systems: Opportunities and Challenges, Advances in Agroforestry, 1st ed.; Kumar, B., Mohan Nair, P.K.R., Eds.; Springer: Dordrecht, The Netherlands, 2011; Volume 17, pp. 17–42. [Google Scholar]
  8. Pardos, J.A. Los Ecosistemas Forestales y el Secuestro de Carbono Ante el Cambio Climático; Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA): Madrid, Spain, 2010; 253p. [Google Scholar]
  9. Van Noordwijk, M.; Coe, R.; Sinclair, F.L. Central Hypotheses for the Third Agroforestry Paradigm within Common Definition; Working Paper, No 233; World Agroforestry Center (ICRAF) Southeast Asia Regional Program: Bogor, Indonesia, 2016; Available online: https://www.cabdirect.org/cabdirect/abstract/20163398164 (accessed on 8 February 2021).
  10. Torquebiau, E. A renewed perspective on agroforestry concepts and classification. Life Sci. 2000, 323, 1009–1017. [Google Scholar] [CrossRef]
  11. Nair, P.K.R. Carbon sequestration studies in agroforestry systems: A reality-check. Agrofor. Syst. 2012, 86, 243–253. [Google Scholar] [CrossRef]
  12. Alvarado, J.; Andrade, H.; Segura, M. Almacenamiento de carbono orgánico en suelos en sistemas de producción de café (Coffea arabica L.) en el municipio del Líbano, Tolima, Colombia. Colomb. For. 2013, 16, 21–31. [Google Scholar]
  13. Nair, P.K.R.; Nair, V.D.; Kumar, B.M.; Showalter, J. Carbon sequestration in agroforestry systems. Adv. Agron. 2010, 108, 237–307. [Google Scholar] [CrossRef]
  14. Brandle, J.R.; Hintz, D.L.; Sturrock, J.W. Windbreak Technology; Elsevier: Amsterdam, The Netherlands, 1988; 598p. [Google Scholar]
  15. Koohafkan, P.; Altieri, M.A. Globally Important Agricultural Heritage Systems: A Legacy for the Future; UN-FAO: Rome, Italy, 2010; 41p. [Google Scholar]
  16. Arévalo-Gardini, E.; Canto, M.; Alegre, J.; Loli, O.; Julca, A.; Baligar, V. Changes in soil physical and chemical properties in long term improved natural and traditional agroforestry management systems of cacao genotypes in Peruvian Amazon. PLoS ONE 2015, 10, e0132147. [Google Scholar] [CrossRef]
  17. Arias, R.M.; Heredia, A.G. Fungal diversity in coffee plantation systems and in a tropical montane cloud forest in Veracruz, Mexico. Agrofor. Syst. 2014, 88, 921–933. [Google Scholar] [CrossRef]
  18. Solis, R.; Vallejos-Torres, G.; Arévalo, L.; Marín-Díaz, J.; Ñique-Alvarez, M.; Engedal, T.; Bruun, T. Carbon stocks and the use of shade trees in different coffee growing systems in the Peruvian Amazon. J. Agric. Sci. 2020, 158, 450–460. [Google Scholar] [CrossRef]
  19. Mortimer, R.; Saj, S.; David, C. Supporting and regulating ecosystem services in cacao agroforestry systems. Agrofor. Syst. 2018, 92, 1639–1657. [Google Scholar] [CrossRef]
  20. Saj, S.; Durot, C.; Mvondo Sajouma, K.; Tayo Gamo, T.; Avana-Tientcheu, M.L. Contribution of associated trees to long-term species conservation, carbon storage and sustainability: A functional analysis of tree communities in cacao plantations of Central Cameroon. Int. J. Agr. Sustain. 2017, 15, 282–302. [Google Scholar] [CrossRef]
  21. Toledo-Hernández, M.; Wanger, T.C.; Tscharntke, T. Neglected pollinators: Can enhanced pollination services improve cocoa yields? A review. Agr. Ecosyst. Environ. 2017, 247, 137–148. [Google Scholar] [CrossRef]
  22. Murray, N.R.M.; Bojórquez, S.J.; Hernández, J.A.; Orozco, M.G.; García., J.D.; Gómez, A.R.; Ontiveros, G.H.; Aguirre, O.J. Efecto de la materia orgánica sobre las propiedades físicas del suelo en un sistema agroforestal de la llanura costera norte de Nayarit, México. Rev. Bio Cienc. 2011, 1, 27–35. [Google Scholar]
  23. Schroth, G.; Jeusset, A.; da Silva Gomez, A.; Florence, C.T.; Pinto Coelho, A.; Faria, D.; Laderach, P. Climate friendliness of cocoa agroforests is compatible with productivity increase. Mitig. Adapt. Glob. Chang. 2016, 21, 67–80. [Google Scholar] [CrossRef]
  24. Andersson, L. Achieving the Global Goals through Agroforestry. Stocolm. Available online: http://agroforestrynetwork.org.hemsida.eu/wp-content/uploads/2018/09/Achieving-the-Global-Goals-through-agroforestry.pdf (accessed on 18 July 2022).
  25. Harvey, C.A.; Komar, O.; Chazdon, R.; Ferguson, B.G.; Finegan, B.; Griffith, D.M.; Martinez-Ramos, M.; Morales, H.; Nigh, R.; Soto-Pinto, L.; et al. Integrating agricultural landscapes with biodiversity conservation in the Mesoamerican hotspot. Conserv. Biol. 2008, 22, 8–15. [Google Scholar] [CrossRef] [Green Version]
  26. Nair, P.K.R. Agroforestry systems and environmental quality: Introduction. J. Environ. Qual. 2011, 40, 784–790. [Google Scholar] [CrossRef] [Green Version]
  27. Preciado, O.; Ocampo, C.; Possú, W.B. Caracterización del sistema de producción tradicional de cacao de cacao (Theobroma cacao L.) en seis núcleos productivos del municipio de Tumaco, Nariño. Rev. Cienc. Agrícolas 2011, 20, 58–69. [Google Scholar]
  28. Espinosa-Alzate, J.A.; Ríos-Osorio, L.A. Caracterización de sistemas agroecológicos para el establecimiento de cacao (Theobroma cacao L.); en comunidades afrodescendientes del Pacífico Colombiano (Tumaco-Nariño, Colombia). Acta Agronómica 2016, 65, 211–217. [Google Scholar] [CrossRef]
  29. Cardenas-Pardo, N.J.; Darghan, A.; Sosa-Rico, M.D.; Rodriguez, A. Spatial analysis of diseases incidence in different cocoa genotypes (Theobroma cacao L.) in Yopal (Casanare).; Colombia. Acta Biol. Colomb. 2017, 22, 209–220. [Google Scholar] [CrossRef]
  30. Agronet. Agricultural Statistics, Cocoa, Production, Yield Share in the Department. Available online: https://www.agronet.gov.co/Documents/6-CACAO_2017.pdf (accessed on 8 February 2021).
  31. Tennhardt, L.; Lazzarini, G.; Weisshaidinger, R.; Schader, C. Do environmentally-friendly cocoa farms yield social and economic co-benefits? Ecol. Econ. 2022, 197, 107428. [Google Scholar] [CrossRef]
  32. Fountain, A.; Huetz-Adams, F. Cocoa Barometer. 2018. Available online: https://voicenetwork.cc/wp-content/uploads/2019/07/2018-Cocoa-Barometer.pdf (accessed on 18 July 2022).
  33. Mithöfer, D.; Roshetko, J.M.; Donovan, J.A.; Nathalie, E.; Robiglio, V.; Wau, D.; Blare, T. Unpacking ‘sustainable’ cocoa: Do sustainability standards, development projects and policies address producer concerns in Indonesia, Cameroon and Peru? Int. J. Biodivers. Sci. Ecosyst. Serv. Manag. 2017, 13, 444–469. [Google Scholar] [CrossRef] [Green Version]
  34. Meier, C.; Sampson, G.; Larrea, C.; Schlatter, B.; Voora, V.; Dang, D.; Bermudez, S.; Wozniak, J.; Willer, H. The State of Sustainable Markets 2020: Statistics and Emerging Trends; ITC: Geneva, Switzerland, 2020. [Google Scholar]
  35. Grabs, J.; Carodenuto, S.L. Traders as sustainability governance actors in global food supply chains: A research agenda. Strateg. Environ. 2021, 30, 1314–1332. [Google Scholar] [CrossRef]
  36. Busquet, M.; Bosma, N.; Hummels, H. A multidimensional perspective on child labor in the value chain: The case of the cocoa value chain in West Africa. World Dev. 2021, 146, 105601. [Google Scholar] [CrossRef]
  37. Ebagnerin Tondoh, J.; N’guessan Kouamé, F.; Martinez Guéi, A.; Sey, B.; Wowo Koné, A.; Gnessougou., N. Ecological changes induced by full-sun cocoa farming in Côte d’Ivoire. Glob. Ecol. Conserv. 2015, 3, 575–595. [Google Scholar] [CrossRef] [Green Version]
  38. Goswami, S.; Verma, K.S.; Kaushal, R. Biomass and carbon sequestration in different agroforestry systems of a Western Himalayan watershed. Biol. Agric. Hortic. 2013, 30, 88–96. [Google Scholar] [CrossRef]
  39. Oelbermann, M.; Voroney, R.P.; Gordon, A.M. Carbon sequestration in tropical and temperate agroforestry systems: A review with examples from Costa Rica and southern Canada Agriculture. Ecosyst. Environ. 2004, 104, 359–377. [Google Scholar] [CrossRef]
  40. Dhyani, S.K.; Ram, A.; Dev, I. Potential of agroforestry systems in carbon sequestration in India. Indian J. Agric. Sci. 2016, 86, 1103–1112. [Google Scholar]
  41. Ballesteros Possu, W.; Brandle, J.R.; Domke, G.M.; Schoeneberger, M.; Blankenship, E. Estimating carbon storage in windbreak trees on U.S. agricultural lands. Agrofor. Syst. 2016, 90, 889–904. [Google Scholar] [CrossRef] [Green Version]
  42. Chirwa, P.W.; Mala, W. Trees in the landscape: Towards the promotion and development of traditional and farm forest management in tropical and subtropical regions. Agrofor. Syst. 2016, 90, 555–561. [Google Scholar] [CrossRef] [Green Version]
  43. Holdridge, L. Ecología Basada en Zonas de Vida; IICA: San José, Costa Rica, 1982; p. 216. [Google Scholar]
  44. Instituto de Hidrología, Meteorología y Estudios Ambientales-IDEAM. Cartas Climatológicas del Aeropuerto la Florida, Tumaco. Nariño. Available online: www.ideam.gov.co (accessed on 10 March 2020).
  45. MacDicken, K.G. A guide to monitoring carbon storage in forestry and agroforestry projects. Report of the forest carbon monitoring program; Winrock Internationl Institute for Agricultural Development: Arlington, VA, USA, 1997; p. 92. [Google Scholar]
  46. Picard, N.; Saint-André, L.; Henry, M. Manual for Building Tree Volumen and Biomass Allometric Equations: From Field Measurement to Prediction; Food and Agricultural Organization of the United Nations: Rome, Italy; Centre de Coopération Internationale en Recherche Agronomique pour le Développement: Montpellier, France, 2012; p. 215. [Google Scholar]
  47. Skog, K.E.; Nicholson, G.A. Carbon cycling through wood products: The role of wood and paper products in carbon sequestration. For. Prod. J. 1998, 48, 75. [Google Scholar]
  48. Jenkins, J.C.; Birdsey, R.A.; Pan, Y. Biomass and NPP estimation for the mid-Atlantic region (USA) using plot-level forest inventory data. Ecol. Appl. 2001, 11, 1174–1193. [Google Scholar] [CrossRef]
  49. Crow, T.R. Biomass and production in three contiguous forests in northern Wisconsin. Ecology 1978, 59, 265–273. [Google Scholar] [CrossRef]
  50. Loetsch, F.; Zohrer, F.; Haller, K.E. Forest Inventory; BLV Verlagsgesellschaft: Munchen, Germany, 1973; p. 469. [Google Scholar]
  51. Box, G.E.P.; Cox, D.R. An Analysis of Transformations. J. R. Stat. Soc. Ser. B 1964, 26, 211–252. [Google Scholar] [CrossRef]
  52. Furnival, G.M. An index for comparing equations used in constructing volume tables. For. Sci. 1961, 7, 337–341. [Google Scholar]
  53. Nakamura, T.; Judd, K.; Mess, M.I.; Small, M. A comparative Study of Information Criteria for Model Selection. Available online: http://staffhome.ecm.uwa.edu.au/~00027830/pdf/IJBC16-2.pdf (accessed on 9 February 2021).
  54. Kutner, M.H.; Nachtsheim, C.J.; Neter, J. Applied Linear Regression Models, 4th ed.; Irwin Inc.: New York, NY, USA, 2004; p. 701. [Google Scholar]
  55. Whitesell, C.D.; Miyasaka, S.C.; Strand, R.F.; Schubert, T.H.; McDuSe, K.E. Equations for Predicting Biomass in 2- to 6-year-old Eucalyptus Saligna in Hawaii; USAD Forest Service Research Notes, PSW-402; Pacific Southwest Forest and Range Experiment Station: Albany, CA, USA, 1988; p. 5. [Google Scholar]
  56. Busing, R.T.; Clebsch, E.E.C.; White, P.S. Biomass production of southern Appalachian cove forests reexamined. Can. J. For. Res. 1993, 23, 60–65. [Google Scholar] [CrossRef]
  57. Andrade, H.; Segura, M.; Somarriba, E.; Villalobos., M. Valoración biofísica y financiera de la fijación de carbono por uso del suelo en fincas cacaoteras indígenas de Talamanca, Costa Rica. Agroforestería En Las Américas 2008, 46, 45–50. [Google Scholar]
  58. Cairns, M.A.; Brown, S.; Helmer, E.H.; Baumgardner, G.A. Root biomass allocation in the world’s upland forests. Oecologia 1997, 111, 1–11. [Google Scholar] [CrossRef]
  59. R Core Team. R: A Language and Environment for Statistical Computing; R Foundation for Statistical Computing: Vienna, Austria, 2013; Available online: https://www.R-project.org/ (accessed on 9 February 2020).
  60. Albrecht, A.; Kandji, S.T. Carbon sequestration in tropical agroforestry systems. Agric. Ecosyst. Environ. 2003, 99, 15–27. [Google Scholar] [CrossRef]
  61. Telles Antonio, R.; Alanís Rodríguez, E.; Jiménez Pérez, J.; Aguirre Calderón, O.A.; Treviño Garza, E.J. Accumulated carbon estimation in Gmelina arborea Roxb. from Tlatlaya.; Estado de México with allometric equations. Rev. Mex. Cienc. For. 2019, 10, 135–153. [Google Scholar] [CrossRef] [Green Version]
  62. Monteith, J.; Chin, L.; Ong, K.; Corlett, J.E. Microclimatic interactions in agroforestry system. For. Ecol. Manag. 1991, 45, 31–44. [Google Scholar] [CrossRef]
  63. Ayegboyin Kayode, O.; Famaye Amos, O.; Adeosun Seun, A.; Idrisu, M.; Ugioro, O.; Asowata, F.E.; Okunade Favour, A. Effect of high density planting on the vigour and yield of Theobroma cacao L. in the Southwest of Nigeria. World J. Adv. Res. Rev. 2020, 8, 217–223. [Google Scholar] [CrossRef]
  64. Spaggiari Souza, C.A.; dos Santos Dias, L.A.; Galeas Aguila, M.A.; Songheti, S.; Oliveira, J.; Andrade Costa, J.L. Cacao yield in different planting densities. Braz. Arch. Biol. Technol. 2009, 52, 1313–1320. [Google Scholar] [CrossRef]
  65. Abou Rajab, Y.; Leuschner, C.; Barus, H.; Tjoa, A.; Hertel, D. Cacao cultivation under diverse shade tree cover allows high carbon storage and sequestration without yield losses. PLoS ONE 2016, 11, e0149949. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  66. Vega, Y. Análisis mensual de acumulación de biomasa y fijación de carbono en una plantación de Gmelina arborea Roxb. Los Chiles, Alajuela, Costa Rica. Ph.D. Thesis, Ingeniero forestal-Instituto tecnológico de Costa Rica, Escuela de Ingeniería Forestal Costa Rica, Alajuela, Costa Rica, 2016; p. 39. [Google Scholar]
  67. Bohre, P.; Chaubey, O.P.; Singhal, P.K. Biomass Accumulation and Carbon Sequestration in Tectona grandis Linn. f. and Gmelina arborea Roxb. Int. J. Bio-Sci. Bio-Technol. 2013, 5, 153–174. [Google Scholar]
  68. Cámara, C.D.C.; Arias, M.; Martínez, S.J.L.; Castillo, A.O. Carbono almacenado en selva mediana de Quercus oleoides y plantaciones de Eucalyptus urophylla y Gmelina arborea en Huamanguillo, Tabasco. In Estado Actual del Conocimiento del Ciclo del Carbono y Sus Interacciones en México: Síntesis a 2013; Pellat, F.P., Julio, W.G., Maira y, B., Saynes, V., Eds.; Universidad Autónoma de Chapingo: Texcoco, Mexico, 2013; p. 702. [Google Scholar]
  69. Melo Cruz, O.A. Modelación del Crecimiento.; Acumulación de Biomasa y Captura de Carbono en Árboles de Gmelina arborea Roxb., Asociados a Sistemas Agroforestales y Plantaciones Homogéneas en Colombia. Ph.D. Thesis, Facultad de Ciencias Agrarias, Universidad Nacional de Colombia, Sede Medellín, Medellín, Colombia, 2015; 166p. [Google Scholar]
  70. Patiño Forero, S.; Suárez Santos, L.N.; Andrade Castañeda, H.J.; Segura Madrigal, M.A. Captura de carbono en biomasa en plantaciones forestales y sistemas agroforestales en Armero-Guayabal, Tolima, Colombia. Rev. De Investig. Agrar. Y Ambient. 2018, 9, 121–134. [Google Scholar] [CrossRef]
  71. Onyekwelu, C.J. Above-ground biomass production and biomass equations for even-aged Gmelina arborea (ROXB) Plantations in South-Western Nigeria. Biomass Bioenergy 2004, 26, 39–46. [Google Scholar] [CrossRef]
  72. Lasco, R.; Come, R.; Estrella, R.; Saplaco, S.R.; Castillo, A.S.A.; Cruz, R.; Pulhin, F. Carbon stock assessment of two agroforestry systems in a tropical forest reserve in the Philippines. Philipp. Agric. Sci. 2001, 84, 401–407. [Google Scholar]
  73. Owusu, S.; Anglaaere, L.C.N.; Abugre, S. Aboveground biomass and carbon content of a cocoa—Gliricida sepium agroforestry system in Ghana. Ghana Jnl Agric. Sci. 2018, 53, 45–60. [Google Scholar] [CrossRef]
  74. Aristizábal, J.; Guerra, A. Estimación de la Tasa de Fijación de Carbono en el Sistema Agroforestal Nogal Cafetero Cordia alliodora, cacao Theobroma cacao y Plátano Musa paradisíaca. Ph.D. Thesis, Ingeniero Forestal, Universidad Distrital, Bogotá, Colombia, 2002; 108p. Available online: http://www.sidalc.net/repdoc/a4836e/a4836e.pdf (accessed on 8 February 2021).
  75. Vespa, A. Relaciones Hídricas e Intercambio de Gases en Theobroma cacao var. Guasare Bajo Períodos de Déficit Hídrico. Rev. Fac. Agron. Univ. Zulia 2008, 2, 112–120. [Google Scholar]
  76. Chijioke, E.O. Impart on Soils of Fast Growing Species in Lowland Humid Tropics; FAO Forestry Paper, No.21; Food and Agricultural Organization: Rome, Italy, 1980; 111p. [Google Scholar]
  77. Schoeneberger, M.M. Agroforestry: Working trees for sequestering carbon on agricultural lands. Agrofor. Syst. 2009, 75, 27–37. [Google Scholar] [CrossRef] [Green Version]
  78. Ruiz-Blandon, B.A.; Hernández-Álvarez, E.; Rodríguez-Macias, R.; Salcedo-Pérez, E. Mensuration assessment and biomass production in Gmelina arborea Roxb. ex Sm. established in pure and mixed stands. Rev. Mex. Cienc. For. 2020, 11, 94–117. [Google Scholar] [CrossRef]
  79. Claesson, S.; SahlTen, K.; Lundmark, T. Functions for biomass estimation of young Pinus sylvestris, Picea abies and Betula spp from stands in Northern Sweden with high sand densities. Scand. J. For. Res. 2001, 16, 138–146. [Google Scholar] [CrossRef]
  80. Nam, V.T.; van Kuijk, M.; Anten, N.P.R. Allometric equations for aboveground and belowground biomass estimations in an evergreen forest in Vietnam. PLoS ONE 2016, 11, e0156827. [Google Scholar] [CrossRef]
  81. Somarriba, E.; Cerda, R.; Orozco, L.; Deheuvels, O.; Cifuentes, M.; Dávila, H.; Espin, T.; Mavisoy, H.; Ávila, G.; Alvarado, E.; et al. Carbon stocks and cocoa yields in agroforestry systems of Central America. Agr. Ecosyst. Environ. 2013, 173, 46–57. [Google Scholar] [CrossRef]
  82. Chave, J.; Andalo, C.; Brown, S.; Cairns, M.A.; Chambers, J.Q.; Eamus, D.; Fölster, H.; Fromard, F.; Higuchi, N.; Kira, T.; et al. Tree allometry and improved estimation of carbon stocks and balance in tropical forests. Oecologia 2005, 145, 87–99. [Google Scholar] [CrossRef]
  83. Montoya-Restrepo, I.A.; Montoya-Restrepo, L.A.; Lowy Cerón, P.D. Oportunidades para la actividad cacaotera en el municipio de Tumaco, Nariño, Colombia. Entramado 2015, 11, 48–59. [Google Scholar] [CrossRef]
  84. Armengot, L.; Barbieri, P.; Andres, C.; Milz, J.; Schneider, M. Cacao agroforestry systems have higher return on labor compared to full-sun monocultures. Agron. Sustain. Dev. 2016, 36, 70. [Google Scholar] [CrossRef] [Green Version]
  85. Beer, J.; Muschler, R.; Somarriba, E.; Kass, D. Shade management in coffee and cocoa plantations. Agrofor. Syst. 1997, 38, 139–164. [Google Scholar] [CrossRef]
  86. Koko, L.K.; Snoeck, D.; Lekadou, T.T.; Assiri, A.A. Cacao-fruit tree intercropping effects on cocoa yield, plant vigour and light interception in Côte d’Ivoire. Agrofor. Syst. 2013, 87, 1043–1052. [Google Scholar] [CrossRef]
  87. Blaser, W.J.; Oppong, J.; Hart, S.P.; Landolt, J.; Yeboah, E.; Six, J. Climate-smart sustainable agriculture in low-to-intermediate shade agroforests. Nat. Sustain. 2018, 1, 234. [Google Scholar] [CrossRef]
  88. Andres, C.; Blaser, W.J.; Dzahini-Obiatey, H.K.; Ameyaw, G.A.; Domfeh, O.K.; Awiagah, M.A.; Gattinger, A.; Schneider, M.; Offei, S.K.; Six, J. Agroforestry systems can mitigate the severity of cocoa swollen shoot virus disease. Agric. Ecosyst. Environ. 2018, 252, 83–92. [Google Scholar] [CrossRef]
  89. Asare, R.; Markussen, B.; Asare, R.A.; Anim-Kwapong, G.; Ræbild, A. On-farm cocoa yields increase with canopy cover of shade trees in two agro-ecological zones in Ghana. Clim. Dev. 2018, 11, 435–445. [Google Scholar] [CrossRef] [Green Version]
  90. Vernon, A.J.; Sundaram, S. Current cocoa research. In Proceedings of the 4th International Cocoa Research Conference, St. Augustine, Trinidad and Tobago, 8–18 January 1972; pp. 689–693. [Google Scholar]
  91. Lahive, F.; Hadley, P.; Daymond, A.J. The physiological responses of cacao to the environment and the implications for climate change resilience. A review. Agron. Sustain. Dev. 2019, 39, 5. [Google Scholar] [CrossRef] [Green Version]
  92. Yalta, H. Identificación y Rentabilidad de Sistemas Agroforestales Asociados al Cultivo de Cacao (Theobroma cacao L.) en Tingo Maria. Ph.D. Thesis, Universidad Nacional Agraria de la Selva, Tingo Maria, Peru, 2003; 101p. [Google Scholar]
  93. Seufert, V.; Ramankutty, N.; Foley, J.A. Comparing the yields of organic and conventional agriculture. Nature 2012, 485, 229–232. [Google Scholar] [CrossRef] [PubMed]
  94. Cerda, R.; Deheuvels, O.; Calvache., D.; Niehaus, L.; Saenz, Y.; Kent, J.; Vilchez, S.; Villota, A.; Martinez, C.; Somarriba, E. Contribution of cocoa agroforestry systems to family income and domestic consumption: Looking toward intensification. Agrofor. Syst. 2014, 88, 957–981. [Google Scholar] [CrossRef]
  95. Notaro, M.; Gary, C.; Deheuvels, O. Plant diversity and density in cocoa-based agroforestry systems: How farmers’ income is affected in the Dominican Republic. Agrofor. Syst. 2020, 94, 1071–1084. [Google Scholar] [CrossRef]
  96. Bisseleua, D.H.B.; Missoup, A.D.; Vidal, S. Biodiversity conservation, ecosystem functioning, and economic incentives under cocoa agroforestry intensification. Conserv. Biol. 2009, 23, 1176–1184. [Google Scholar] [CrossRef]
  97. Egbewole, Z.T.; Falade, L.O.; Rotowa, O.J.; Kuje, E.D.; Mairafi, H.H. Evaluation of the Effect of Agricultural Crop on the Growth Performance of Gmelina arborea under Agroforestry System. Available online: https://www.researchgate.net/publication/343502140_Evaluation_of_the_Effect_of_Agricultural_Crop_on_the_Growth_Performance_of_Gmelina_arborea_under_Agroforestry_System (accessed on 18 July 2022).
  98. Jose, S.; Bardhan, S. Agroforestry for biomass production and carbon sequestration: An overview. Agrofor. Syst. 2012, 86, 105–111. [Google Scholar] [CrossRef]
  99. Biswas, B.; Chakraborty, D.; Timsina, J.; Rudra Bhowmick, U.; Pratap Kumar, D.; Dipak Kumar, G.; Sarkar, A.; Mondal, M.; Adhikary, S.; Kanthal, S.; et al. Agroforestry offers multiple ecosystem services in degraded lateritic soils. J. Clean. Prod. 2022, 365, 132768. [Google Scholar] [CrossRef]
  100. Intergovernmental Panel on Climate Change. Global Warming of 1.5 °C. An IPCC Special Report on the Impacts of Global Warming of 1.5 °C above Pre-Industrial Levels and Related Global Greenhouse Gas Emission Pathways, in the Context of Strengthening the Global Response to the Threat of Climate Change, Sustainable Development, and Efforts to Eradicate Poverty; Masson-Delmotte, V., Zhai, P., Pörtner, H.-O., Roberts, D., Skea, J., Shukla, P.R., Pirani, A., Moufouma-Okia, W., Péan, C., Pidcock, R., et al., Eds.; IPCC: Geneva, Switzerland, 2018; 630p. [Google Scholar]
  101. United Nations Organization. Sustainable Development Goals. Available online: https://www.un.org/sustainabledevelopment/climate-change/ (accessed on 18 July 2022).
  102. Kuyah, S.; Whitney, C.W.; Jonsson, M.; Sileshi, G.W.; Öborn, I.; Muthuri, C.W.; Luedeling, E. Agroforestry delivers a win-win solution for ecosystem services in sub-Saharan Africa. A meta-analysis. Agron. Sustain. Dev. 2019, 39, 47. [Google Scholar] [CrossRef] [Green Version]
  103. Carsan, S.; Stroebel, A.; Dawson, I. Can agroforestry option values improve the functioning of drivers of agricultural intensification in Africa? Curr. Opin. Environ. Sustain. 2014, 6, 35–40. [Google Scholar] [CrossRef] [Green Version]
  104. Syampungani, S.C. The potential of using agroforestry as a win-win solution to climate change mitigation and adaptation and meeting food security challenges in Southern Africa. Agric. J. 2010, 5, 80–88. [Google Scholar] [CrossRef] [Green Version]
  105. Nunoo, I.; Fromm, I.; Frimpong, B.N. Factors Influencing the Adoption of Cocoa Agroforestry Systems in Mitigating Climate Change in Ghana: The Case of Sefwi Wiawso in Western Region. Environ. Sustain. Clim. Chang. 2020, 2, 1–4. Available online: https://researchopenworld.com/wp-content/uploads/2020/07/ESCC-2-1-202.pdf (accessed on 18 July 2022).
Figure 1. Study area: Consejo Comunitario Rescate Las Varas.
Figure 1. Study area: Consejo Comunitario Rescate Las Varas.
Sustainability 14 09447 g001
Figure 2. Aboveground carbon storage potential of G. arborea (A), and T. cacao (B) agroforestry arrangements. Aboveground carbon storage potential of agroforestry arrangements (C), and total above and belowground carbon storage potential of agroforestry system (D), a–d: statistical significance indices: “Means with the same letter are not significantly different”.
Figure 2. Aboveground carbon storage potential of G. arborea (A), and T. cacao (B) agroforestry arrangements. Aboveground carbon storage potential of agroforestry arrangements (C), and total above and belowground carbon storage potential of agroforestry system (D), a–d: statistical significance indices: “Means with the same letter are not significantly different”.
Sustainability 14 09447 g002aSustainability 14 09447 g002b
Figure 3. Average cocoa yield (A), soil bulk density (B), and soil organic matter (C) in a different AFS. a,b,c: Statistical significance indices: “Means with the same letter are not significantly different”.
Figure 3. Average cocoa yield (A), soil bulk density (B), and soil organic matter (C) in a different AFS. a,b,c: Statistical significance indices: “Means with the same letter are not significantly different”.
Sustainability 14 09447 g003
Table 1. Treatments, spacing, and density of cacao and Melina trees in the experimental design.
Table 1. Treatments, spacing, and density of cacao and Melina trees in the experimental design.
TreatmentsCacaoMelina
Spacing (m2)Trees/haSpacing (m2)Trees/ha
13 × 311113 × 31111
24 × 46254 × 4625
33 × 48338 × 6208
43 × 483312 × 6139
53 × 483316 × 6104
63 × 48333 × 3 × 7.5440
7 *7 × 720012 × 1269
* Traditional cocoa production system (control).
Table 2. Allometric equations used to estimate the biomass potential of AFS.
Table 2. Allometric equations used to estimate the biomass potential of AFS.
NumberAuthorEquation
1Berkhoutbm = a + b × dbh
2Kopezkybm = a + b × dbh2
3Hohenadl-Krennbm = a + b × dbh + c × dbh2
4HuschLn bm = a + b × ln dbh
5Spurrbm = a + b × dbh2 × ht
6Stoatebm = a + b × dbh2 + c × dbh2 × ht + d × ht
7Meyerbm = a + b × dbh2 + c × dbh2 × ht + d × dbh2 × h
8Schumacher-HallLog bm = a + b × ln dbh + c × ln × ht
9BrenackLog bm = a + b × dbh + c × 1/dbh
10This studySqrt (bm) = a + b × dbh
11This studybm = a + b ln(dbh) + ln(ht)
12This studySqrt (bm) = a + b × dbh + c × ht
13This studybm = a × exp(b × dbh)
14This studybm = a × dbh^b
15This studybm = a + b ln(dbh))
Source: Loetsch et al. [50]. bm = biomass (kg/tree) or C (kg/tree); dbh = diameter at the breast height (1.30 m), ht = total height (m); a, b, c, d = model parameters; ln = logarithm base e = 2.718282.
Table 3. Performance of the different competing allometric models in the information criteria indexes.
Table 3. Performance of the different competing allometric models in the information criteria indexes.
ModelR2AICBICPRESSCpVIFFI
10.93399.7404560.314.41.03.9
20.93401.6406.455.816.51.059.1
30.9340040548.25.814.533.8
40.91399.8404.5153.62.001.065.8
50.9370.866.00134. 816.4139.659.8
60.94405.5410.20.302.80144.819.4
70.94401.6407.90.3015.266.13.8
80.9170.866.00155.518.713.767.5
90.9168.862.5150.11.80144.865.5
100.92118.0125.9143.12.801.062.6
110.92403.5411.4134.817.4124.560.6
120.92114.6119.3147.74.8013.763.3
130.93402.9412.4155.52.601.07.4
140.93402.8413.9134.95.601.033.24
150.93399.8404.516016.41.068.7
R2 = Determination coefficient; AIC = Akaike information criteria; BIC = Bayesian information criteria; PRESS = predicted residual sum of squares; VIF = Variance inflation factor; FI = Furnival index.
Table 4. Competing allometric models selected to make biomass estimates for G. arborea.
Table 4. Competing allometric models selected to make biomass estimates for G. arborea.
Model NumberModel 1R2αβMSPERank
1Berkouth0.93−534.33933.2825.741
14This study 30.931.80481.64695.782
4Husch0.910.39821.69825.823
10This study 10.924.647710.582195.844
2Kopezky0.93141.540960.397945.895
15This study 40.93−4153.611346.996.116
13This study 20.931640.03866.217
1 35 trees for model training and 1 tree drawn at random (testing) without replacement to evaluate the precision of each model repeated in 8 different trees. α, and β are regression coefficients, R2 = Adjusted determination coefficient, MSPE = mean square prediction error.
Table 5. Metrics of the financial analysis to estimate the profitability of the different agroforestry arrangements in San Luis Robles—Tumaco, Nariño.
Table 5. Metrics of the financial analysis to estimate the profitability of the different agroforestry arrangements in San Luis Robles—Tumaco, Nariño.
TreatmentsNPV1IRR (%)BCR
11,737,024261.14
21,262,004251.16
31,308,798301.22
41,302,763291.20
51,287,711291.18
61,446,457421.67
7651,650131.02
NPV1 = Net Present Value (Colombian pesos -$ COP); IRR = Internal Rate of Return; BCR = Benefit-Cost Ratio.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Ballesteros-Possú, W.; Valencia, J.C.; Navia-Estrada, J.F. Assessment of a Cocoa-Based Agroforestry System in the Southwest of Colombia. Sustainability 2022, 14, 9447. https://doi.org/10.3390/su14159447

AMA Style

Ballesteros-Possú W, Valencia JC, Navia-Estrada JF. Assessment of a Cocoa-Based Agroforestry System in the Southwest of Colombia. Sustainability. 2022; 14(15):9447. https://doi.org/10.3390/su14159447

Chicago/Turabian Style

Ballesteros-Possú, William, Juan Carlos Valencia, and Jorge Fernando Navia-Estrada. 2022. "Assessment of a Cocoa-Based Agroforestry System in the Southwest of Colombia" Sustainability 14, no. 15: 9447. https://doi.org/10.3390/su14159447

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

Article Metrics

Back to TopTop