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The Impact of Carbon Dioxide Concentrations and Low to Adequate Photosynthetic Photon Flux Density on Growth, Physiology and Nutrient Use Efficiency of Juvenile Cacao Genotypes

USDA-ARS-Beltsville Agricultural Research Center, Beltsville, MD 20705, USA
Department of Biological Science, State University of Santa Cruz, Ilhéus, BA 45650-000, Brazil
IRREC, Institute of Food and Agriculture Sciience, University of Florida, Fort Pierce, FL 34945, USA
Author to whom correspondence should be addressed.
Agronomy 2021, 11(2), 397;
Received: 25 January 2021 / Revised: 18 February 2021 / Accepted: 19 February 2021 / Published: 23 February 2021
(This article belongs to the Special Issue Advances in Understanding Physiological Processes of the Cacao Tree)


Cacao (Theobroma cacao L.) was grown as an understory tree in agroforestry systems where it received inadequate to adequate levels of photosynthetic photon flux density (PPFD). As atmospheric carbon dioxide steadily increased, it was unclear what impact this would have on cacao growth and development at low PPFD. This research evaluated the effects of ambient and elevated levels carbon dioxide under inadequate to adequate levels of PPFD on growth, physiological and nutrient use efficiency traits of seven genetically contrasting juvenile cacao genotypes. Growth parameters (total and root dry weight, root length, stem height, leaf area, relative growth rate and net assimilation rates increased, and specific leaf area decreased significantly in response to increasing carbon dioxide and PPFD. Increasing carbon dioxide and PPFD levels significantly increased net photosynthesis and water-use efficiency traits but significantly reduced stomatal conductance and transpiration. With few exceptions, increasing carbon dioxide and PPFD reduced macro–micro nutrient concentrations but increased uptake, influx, transport and nutrient use efficiency in all cacao genotypes. Irrespective of levels of carbon dioxide and PPFD, intraspecific differences were observed for growth, physiology and nutrient use efficiency of cacao genotypes.

1. Introduction

Cacao (Theobroma cacao L) is native to the understory of the Amazonian forests of South America. As an understory plant, it has physiological characteristics similar to those of other shade-adapted species [1,2,3,4]. Growth and development of young cacao trees are better under shade; however, heavy shade is detrimental to growth and production of matured and older trees [5,6,7,8]. Cocoa is a C3 species and prefers full sun, but is tolerant to moderate shading, due to its phenotypic plasticity for acclimatization in moderate shade conditions [9]. However, it does not tolerate dense shade, where pod production is low, even with adequate water levels and mineral nutrients availability in the soil. However, when the cacao tree is grown in full sun, there can be no limitations of water and mineral nutrients in the soil. In a long-term field study in Ghana, Amelonado cacao trees in full sun yielded three times as much as shaded trees; however, the economic life of unshaded trees did not last more than 10 years of intensive cropping due to infestation of diseases and insects and loss of needed soil nutrients [10]. There is no universal agreement on the degree of shade required to maximize production of cacao grown under different tropical ecosystems of the world [9,11,12,13].
In the major cacao growing regions of South and Central America, cacao is often grown as an understory plant in agroforestry systems (AFSs) [9,14,15]. In AFSs, various types of managed and unmanaged single and multi-strata systems are used where cacao is planted together with different types of shade trees, such as timber, fruit, firewood and leguminous trees, and in some cases tree species retained from thinned native forests [16,17,18,19,20,21,22]. In these management systems, cacao is subjected to various levels of low light quantity and quality at its canopy level depending upon the density of single or multi-strata shade trees, the nature and level of vegetative cover and the extent of shade tree pruning [12,23,24]. Shade trees in multi-strata AFSs are known to moderate the microclimatic conditions thereby improving cacao sustainability and providing other sources of income for farmers [6,17,24,25,26].
The amount of light falling on a cacao tree is known to affect its growth and yield, and moderate shade tends to reduce water and nutrient stress [6,12,27]. Optimum growth of young cacao plants was achieved at 20% to 30% of full sunlight [1,28,29]. However, maximum yield of adult plants requires limited shade or full sun especially in areas of ecosystems with heavy cloud cover [8]. Maximum photosynthesis in cacao leaves occurs at a PPFD of 350 to 550 µmol m−2 s−1, which is about 20% to 25% of the intensity of full sunlight [30,31,32,33]. In some young cacao genotypes, an increase of PPFD from 50 to 400 µmol m−2 s−1 increased the net photosynthetic rate (PN) by about 50%, but further increases (up to 1500 µmol m−2 s−1) had no effect, indicating that very little radiant energy is required to support efficient PN in cacao [30].
In shaded cacao plantations in Bahia Brazil, light intensity at noon above the cacao canopy ranged between 30% and 100% of full daylight [34]. Niether et al. [24] reported that cacao received 39% of full sunlight in an agroforestry system in Bolivia. Increasing PPFD from 65 to 1050 µmol m−2 s−1 reduced the growth and concentrations of several macro–micro nutrients in cacao [35]. Depending on the photosynthetic characteristics of the shade tree canopy and its density, different levels of blue and red light are absorbed and/or transmitted; therefore, light reaching field grown understory plants could be low in photosynthetically active radiation and with low R/FR ratio [36,37].
The concentration of CO2 [CO2] in the atmosphere also affects growth of cacao. The present CO2 concentration is around 400 µmol mol−1 and based on the Representative Concentration Pathway selected (RCP of 4.5 to 8.5) and future emission scenarios, CO2 could reach as high as 550 to 1370 µmol mol−1 by the end of the 21st century [38,39].
Overall, elevated [CO2] increases plant growth (shoot and root biomass, leaf and root area, RGR) and physiological parameters (photosynthesis, water use efficiency, and nutrient uptake), however, the magnitude of such responses is dependent on availability of water and nutrients, and environmental variables such as light and temperature [1,30,35,40,41,42,43,44,45,46]. In cacao, increasing [CO2] increased shoot, root and leaf growth, macro–micro nutrient use efficiency, photosynthesis and water use efficiency (WUE) traits; however, the magnitude of such responses to increased [CO2] in cacao depended on the levels of PPFD and genotypes involved [30,35,46,47].
Soils in the cacao growing regions of the world are often acidic, infertile and invariably deficient in nitrogen (N), potassium (K), phosphorus (P), calcium (Ca), magnesium (Mg), zinc (Zn) and iron (Fe), and that leads to severe essential nutrients deficiencies in cacao [11,12,29,48,49,50,51,52]. Increasing atmospheric [CO2] coupled with low soil fertility and low irradiance subject cacao to severe nutrient stress and results in decline of yield potentials. Cacao has considerable genetic variation in morphological and physiological traits [4,53,54,55]. Such traits could be exploited in the selection of genotypes that have higher essential nutrient use efficiency under these abiotic stresses to generate cultivars more adapted to these conditions. Interactions between genotype and environmental factors may allow some genotypes to perform better in changing PPFD and CO2 conditions. The objectives of this research were to assess the influence of ambient and elevated levels of [CO2] and low to adequate photosynthetic photon density (PPFD) on the growth, and physiological traits and macro–micro nutrient uptake, influx and transport and use efficiency in seven genetically contrasting cacao genotypes.

2. Materials and Methods

2.1. Cacao Genotypes

In total, 7 cacao genotypes (Catongo, Coca 3370/5, CCN 51, Amaz 15, LCT EEN 37/A, Na 33 and SCA 6) were used for this study. Pods of these genotypes were received from MARS Center for Cocoa Science (MCCS) Almirante, Itajuipe, Bahia, Brazil. Catongo is from the lower Amazon region of Brazil; Amaz 15, NA 33 and SCA 6 are from the upper Amazon region of Peru; whereas LCT EEN 37A and Coca 3370/5 are from the upper Amazon region of Ecuador; and CCN 51 is a hybrid from Ecuador. These genotypes have been widely distributed in most of the cacao producing countries and some have been commonly used as parental or as cultivars in cacao breeding programs. Genetic background, origin and diseases resistance of these genotypes are covered in Bartley [56], Turnbull and Hadley [57], and Ahnert and Eskes [58]. Seeds were produced by self-pollination of plants. In the case of self-incompatible plants, they were obtained by the mixture of Herrania and cacao pollen, which helps to break self-incompatibility. Therefore, the self-pollinated family plants generated by such seeds have, on an average, similar traits to the parents, in this case, clonal cuttings. Findings of this study had a good scientific interest, showing differences between different genetic populations.

2.2. Plants and Growth Medium

Growth medium was prepared containing sand: perlite: peat moss (2:2:1 volume) supplemented with essential nutrients (mg/kg) 600 N, 600 P, 240 K, 1012 Ca, 309 Mg, 500 S, 119 Fe, 0.7 B, 17.5 Mn, 7 Cu, 7 Zn, and 0.35 Mo. Nutrients were applied as Osmocote 18-6-12 (The Scotts Company, Marysville, Ohio, USA), triple superphosphate, urea, calcium sulphate, dolomitic lime and Scott’s Micromix. Cacao seeds were removed from the pods, surface-sterilized with 10% bleach for 2 min, rinsed twice in Deionized-water, then soaked in 90% ethanol for 2 min and rinsed twice in DI water. Seeds were germinated on sterile moist filter paper for 48 h at 25 °C. Seeds with 2 mm radicle were planted in 3.8 L black plastic pots with adequate bottom drainage containing 2.2 kg of the growth mixture. One seedling was planted in each pot. Soil moisture was maintained near field capacity (−33kPa) by adding water every other day. An initial plant harvest was collected at 21 days after planting. The remaining plants were grown for additional 90 days.

2.3. CO2 and PPFD Treatments

The experiment was conducted in two glasshouses (18 m2 each) at Beltsville, MD and plants were grown with day/night temperatures of 30/28 °C. In the first glasshouse, ambient [CO2] of 400 ± 50 μmol mol−1 was maintained and in the second glasshouse elevated [CO2] of 700± 50 μmol mol−1 was maintained throughout the growth period. In the second glasshouse if [CO2] fell below 700 μmol mol−1 a WMA4 CO2 analyzer (PP Systems, Amesbury, MA, USA) injected the desired amount of CO2. After 55 days of growth, plants were swapped from one glasshouse to the other and [CO2] levels were readjusted in each glasshouse as per the treatments. Within each glasshouse, electrical fans continuously circulated the air at an air speed of 0.5 m s−1 over the plants. Daytime air temperatures were maintained for 12h per day beginning at 6 AM. The greenhouses transmitted approximately 60% of the incident PPFD daily. A data logger (21x, Campbell Scientific, Logan, UT, USA) recorded the PPFD, temperature and [CO2] in both glasshouses at 30–s intervals.
In both glasshouses, plants were grown at three levels of photosynthetic photon flux density (PPFD) (100 ± 20, 200 ± 20 and 400 ± 20 µmol m−2 s−1). To achieve these three levels of irradiance, mini-chambers were constructed with 2 cm (3/4 inch) diameter PVC pipe with overall dimensions of 114 cm W × 119 cm L × 81 cm H (45” × 47” × 32”). To achieve three different levels of PPFD, the tops and sides of the mini chambers were covered with three types of plastic mesh shade cloth: a single-ply of 70% smoke blue sun screen fabric (Easy Gardener, Waco TX) for low PPFD (100 µmol m−2 s−1), a single-ply of black fiberglass window screen (New York Wire, Mt. Wolf, PA, USA) for medium PPFD (200 µmol m−2 s−1) and a single-ply of 22% white shade cloth (National Tool Grinding, Inc, Erie, PA, USA) for high PPFD (400 μmol m−2 s−1). Each mini chamber was covered with mesh shade cloth so they have full air exchange with the environment. In each mini chamber the plants were rotated once per week to keep the light exposures consistent. The light levels in each mini chamber were measured at mid-day with a LI-190S quantum sensor (Li-Cor Inc., Lincoln, NE, USA). All experimental units were replicated three times and each experimental unit had a control pot with no plant in order to quantify evaporation.

2.4. Determination of Plant Physiological Parameters

A week before plant harvest, net photosynthesis [PN, µmol CO2 m−2 s−1], stomatal conductance [gs, mmol H2O m−2 s−1], internal leaf CO2 [Ci, µmol mol−1] and rate of transpiration [E, mmol H2O m−2 s−1] were measured on the fully expanded sixth leaf from top of each plant using a CIRAS-2 Portable Photosynthesis System (PP Systems, Amesbury, MA, USA). The artificial light source was adjusted to the PPFD of the treatments (100, 200 and 400 µmol m−2 s−1). The CO2 flux was adjusted to 400 or 700 µmol mol−1 depending on treatment. The leaf chamber temperature was constant at 30°C. Readings were recorded after 15 min of equilibration. A SPAD meter (Konica Minolta Chlorophyll Meter, Model 502, Ramsey, NJ, USA) was used to determine SPAD index which could be useful to estimate the chlorophyll content of the leaves.
Water Use Efficiency (WUE) was determined by the following equations:
Total Water Use Efficiency, WUETotal = g shoots dry wt. plant−1/g H2O transpired plant−1 over 90 days of growth
Instantaneous water use efficiency, WUEInst = PN/E, µmol CO2/mmol H2O
Intrinsic water use efficiency, WUEIntr = PN/gs, µmol CO2/mmol H2O
Where PN (µmol CO2 m−2 s−1) is net photosynthetic rate, E (mmol H2O m−2 s−1) is transpiration rate, and gs (mmol H2O m−2 s−1) is stomatal conductance. These parameters were obtained from CIRAS-2 portable photosynthesis system measurements.

2.5. Determination of Plant Growth Parameters

After a growth period of 90 days, plants were harvested. Shoots were divided into stems and leaves and weighed. Total leaf area (cm2) was measured using a LI-3100 leaf area meter (Li-Cor Inc., Lincoln, NE, USA). Shoots were washed in deionized water, freeze-dried and dry weight was recorded. The roots were removed from the soil, washed, blotted dry and weighed. Root lengths (cm plant−1) were determined with a Comair Root Length Scanner (Hawker de Haviland, Melbourne, Victoria, Australia) and the roots were oven-dried at 70°C for 5 days and the dry weights were recorded.
Additional growth parameters were calculated by the following formulas:
Leaf area ratio (LAR, cm2/g) = [total leaf area, cm2/shoot+ root dry wt, g]
Specific Leaf Area (SLA, cm2/g) = [Total leaf area/plant, cm2/Total leaf dry wt./plant, g]
Leaf mass/unit leaf area (LMA, g/cm2) = [1/SLA]
Root/shoot ratio (R/S) = [Wr/Ws], where Wr is root dry wt. and Ws is shoot dry wt.
Root Radius (RR, cm) = (RFW/RL × π)1/2 where RFW is root fresh wt. (cm3)
Relative growth rate (RGR, g g−1 day−1) = [ln (Wt2/Wt1)/(T2−T1)], where Wt is total wt. (shoot+root), T is time in days, subscripts 1 and 2 refer to initial and final plant harvest.
Net assimilation rate (NAR, g cm−2 day−1) = [RGR/LAR]

2.6. Determination of Nutrient Uptake Parameters

Dried stems and leaves were ground together to pass through a 1 mm sieve and sent to University of Florida, Indian River Research and Education Center (UF-IRREC), Fort Pierce, FL, USA. for macro–micro nutrient analysis. Plant samples of 0.4 g were digested in 5 mL of concentrated nitric acid (14 N), and macro–micro nutrient concentrations in the digested solutions were determined by using inductively coupled plasma optical emission spectrometry (ICPOES, Ultima JY Horiba Inc. Edison, NJ, USA) [59]. Total N in the plant tissue was analyzed by combustion method using a CN Analyzer (Vario MAX CN Elementar Analysensysteme GmbH, Hanau, Germany) [60].
Nutrient uptake (U), influx (IN), transport (TR) and nutrient use efficiency ratios (ER) were calculated using the following formulas:
Uptake (U) = (Conc. of any given element) × shoot dry wt.
Influx (IN) = [(U2 − U1)/(T2 − T1)] [(lnWr2 − lnWr1)/(Wr2 − Wr1)], where U refers to elemental content in shoot (mmol/plant), T is time in seconds, Wr is root dry wt., and subscripts 1 and 2 refer to initial and final plant harvest times.
Transport (TR) = [(U2 − U1)/(T2 − T1)] [(lnWs2 − lnWs1)/(Ws2 − Ws1)], where Ws is shoot dry weight.
Nutrient Use Efficiency (NUE) = [mg of Ws/mg of any given element in shoot]

2.7. Statistical Analysis

Experiment was split plot design with [CO2] as main plots, PPFD as subplots and genotypes as sub-sub plots and experimental units were replicated three times. All data were analyzed for statistical significance by ANOVA in SAS (Ver. 9.3, SAS Institute, Cary, NC, USA).

3. Results and Discussion

3.1. Growth Traits

Irrespective of [CO2] and PPFD, significant intraspecific differences between cacao genotypes were observed for total and root wt., root length, stem height, leaf area, specific leaf area, relative growth rate (RGR) and net assimilation rates (NAR) (Table 1). Overall, Amaz 15 genotype had higher total and root growth parameters than any of the other genotypes studied. Genetic, physiological and morphological determinants and their interactions with environmental variables such as levels of PPFD and [CO2] profoundly influence the growth, development and nutrient use efficiency of cacao [9,30,35,46]. Variation in morphological characteristics among cacao genotypes has been reported [4,53,54,55] and these morphological characteristics are known to be influenced by levels of PPFD and [CO2] [1,13,35,45,46,61].
In the current study with exception of root/shoot ratio, all the growth traits of shoots and roots in cacao genotypes were significantly influenced by the level of [CO2]. Irrespective of PPFD levels, increasing [CO2] from 400 to 700 µmol mol−1 increased all growth traits except SLA which decreased with increasing [CO2]. In many perennial tropical legume cover crops Baligar et al. [62,63] reported that increasing [CO2] from ambient (400 µmol mol−1) to elevated (700 µmol mol−1) increased growth traits (dry biomass of shoot, leaf and roots, RGR and NAR). Generally, C3 plants respond positively to increased [CO2] above 370 µmol mol−1 [64,65,66]. In the current study, increasing [CO2] significantly increased total leaf area in all the genotypes. Lahive et al. [46] reported increased leaf area in Amelonado cacao genotype grown at elevated [CO2], however, in a recent study, Hebbar et al. [47] found no significant differences in leaf area between cacao grown at 400 and 700 µmol mol−1 [CO2]. In the current study, increasing [CO2] from 400 to 700 µmol mol−1 increased average root dry weight and root length by 0.97 to 2.32 g plant−1 and 2962 to 4974 cm plant−1 respectively. At elevated [CO2], it seems that allocation of carbon fixed by photosynthesis to the roots is as high as that to the shoots. Elevated [CO2] often increases the R/S ratio and fine-root proliferation [43].
In all the cacao genotypes studied, all the growth parameters were significantly influenced by levels of PPFD. Shade tolerant species including cacao are known to respond positively to elevated [CO2], however such enhanced growth response is also governed by light levels [35,46,67,68]. Irrespective of levels of [CO2], increasing PPFD from 100 to 400 µmol m−2 s−1 increased growth traits (total and root weight, stem height, root length, total leaf area, RGR and NAR). However specific leaf area (SLA) was reduced with increasing PPFD indicating that increasing PPFD increases the thickness of the leaves. In cacao genotypes, heavier shade may increase leaf area [19]. Such an adaptation seems to maximize the photon capture capacity of the leaves [45]. Irrespective of [CO2], increasing PPFD from 100 to 400 µmol m−2 s−1 increased average root weight and root length by 1.34 to 1.84 g plant−1 and 3443 to 4357 cm plant−1, respectively. This indicates an increased allocation of carbon fixed through photosynthesis to roots at higher PPFD. Aerial morphological characteristics could have great implications on the ability of plants to intercept and utilize solar radiation and these characteristics in cacao are influenced by level of irradiance [1,9,13,35,45,61].

3.2. Physiological and Water Use Efficiency Traits

Significant intraspecific differences were observed for SPAD index, net photosynthesis (PN), stomatal conductance (gs), internal CO2 (Ci) and transpiration (E) irrespective of levels of [CO2] and PPFD (Table 2). Amaz 15 had higher PN than any other cacao genotype at all levels of [CO2] and PPFD evaluated. This genotype also had the highest leaf area per plant. Increasing [CO2] from ambient to 700 µmol mol−1 has been shown to increase PN in C3 plants [44]. In the current study irrespective of PPFD levels, increasing [CO2] from 400 to 700 µmol mol−1 resulted in a significant increase in PN of all cacao genotypes from an average of 2.47 to 3.41 µmol CO2 m−2 s−1. In an earlier study with 1.5-year-old cacao plants, increasing [CO2] from 370 to 680 μmol mol−1 resulted in a 33% increase in PN [30]. In cacao genotype Amelonado, increasing [CO2] from 460 to 735 μmol mol−1 increased PN by 56% [46]. Recently Hebbar et al. [47] in an open top camber study with cacao reported an increase in PN of 29% by increasing [CO2] from 400 to 700 μmol mol−1. Increasing photosynthesis with increasing [CO2] reported in these studies is typical of responses observed in other C3 plants [69,70].
Levels of aerial [CO2] have significant effects on gs activity. In all the cacao genotypes studied, irrespective of PPFD levels, increasing [CO2] from 400 to 700 µmol mol−1 resulted in a significant reduction in gs from an average of 19.5 to 12.6 mmol H2O m−2 s−1. In leaves of annual C3 plants, doubling of [CO2] reduced gs by 34% [69]. In an earlier study with cacao genotypes, Baligar et al. [30] reported around a 65% reduction in gs by increasing [CO2] from 370 to 700 μmol mol−1. Such a large decrease in gs led to a substantial reduction in E, which could improve cacao water status and drought resistance. Elevated [CO2] has been shown to reduce E and gs in most C3 plants [69]. However, Lahive et al. [46] reported that CO2 concentrations of ambient (average of 466 µmol mol−1) and elevated (average of 725 µmol mol−1) did not have an effect on gs in cacao genotype Amelonado. Stomatal conductance (gs) plays a vital role in regulating PN, transpiration (E), leaf temperature and plant water stress tolerance [13,71,72].
Irrespective of the levels of PPFD, increasing [CO2] from 400 to 700 µmol mol−1 resulted in a significant reduction in transpiration (E) from an average of 0.267 to 0.172 mmol m−2 s−1. A large decrease in gs, as observed in the current study, with increasing [CO2] could lead to reduced E and such changes could improve water status and drought resistance of cacao. Baligar et al. [30] reported that increasing [CO2] from 85 to 850 µmol mol−1 significantly decreased E from 0.66 to 0.16 mmol m−2 s−1 in three cacao genotypes.
It has been widely reported that maximum photosynthesis (PN) in cacao occurs at PPFD of 350 to 550 µmol m−2 s−1 [30,31,32,33]. The limited PPFD received at cacao canopy levels might be the reason for lower yields in agroforestry systems [73]. In the seven cacao genotypes in the current study, irrespective of [CO2], increasing levels of PPFD from 100 to 400 µmol m−2 s−1 resulted in significant increases in PN from an average of 2.67 to 3.41 µmol m−2 s−1. In an earlier study with three genetically differing cacao genotypes, Baligar et al. [30] reported that increasing PPFD from 50 to 400 µmol m−2 s−1 significantly increased PN. However, PN at 50 µmol m−2 s−1 of PPFD was about two-thirds of the maximum 3 µmol CO2 m−2 s−1 indicating that cacao needs very little radiant energy to support its PN. Higher rates of PN, thicker leaves and high rates of E have been observed in certain cacao genotypes when grown in full sunlight rather than under shade [1]. Increasing PPFD from 100 to 400 µmol m−2 s−1 reduced specific leaf area from an average of 284.7 to 227.7 cm2 g−1, such increases in leaf thickness might contribute to higher PN. However, exposure of leaves to extremely high light for longer periods may lead to photoinhibition and lower PN [34,41,42]. Baligar et al. [35] reported that PPFD of 1050 μmol m−2 s−1 was detrimental to shoot, root and leaf growth of cacao seedlings. In all the cacao genotypes studied irrespective of levels of [CO2], increasing levels of PPFD from 100 to 400 µmol m−2 s−1 resulted in significant increases in gs and E from an average of 15.33 to 19.35 mmol H2O m−2 s−1 and 0.215 to 0.258 mmol H2O m−2 s−1, respectively. In an earlier short-term study, Baligar et al. [30] reported that the gs was not significantly affected by PPFD over the observed range of 50 to 400 µmol m−2 s−1; however, there was a slight increase in E, but the relationship between E and PPFD was not significant. Under artificial shade, the quality of the PPFD that reaches the canopy of cocoa leaves is very different from the quality of the PPFD that reaches the canopy of cocoa trees leaves grown in field conditions and shaded by tree species. In field conditions, there is an attenuation of both the intensity and the quality of the light available for cocoa photosynthesis, depending on the greater or lesser absorbance and/or transmittance of electromagnetic light, mainly in the blue and red bands, which crosses canopy strata of different shade tree species. Depending on the photosynthetic characteristics of the shade tree canopy, different levels of PPFD blue and red light are absorbed and/or transmitted, which can affect net photosynthesis differently from cocoa grown under artificial shade. Therefore, obtained results of PN are based on cacao genotypes subjected to ambient and elevated levels of [CO2] under various levels of artificial shade.
Intraspecific differences in WUE traits (WUETotal, WUEInst and WUEIntr) between the cacao genotypes were observed but the differences were not significant (Table 2). Amaz 15 had the highest WUEInst and WUEIntr, which is a reflection of its high PN compared to the other cacao genotypes. In eight contrasting cacao genotypes, variations in WUEInst and WUEIntr were negatively related to specific leaf area [4]. In the current study, all three WUE traits increased with decreasing specific leaf area. In the seven cacao genotypes studied, increasing PPFD and [CO2], increased WUE traits. Increasing [CO2] from 400 to 700 µmol mol−1 caused significant increases in all three water use efficiency traits (WUETotal, WUEInst and WUEIntr). Such significant increases in WUEInst and WUEIntr traits at elevated [CO2] could be related to increased PN and reduced gs and E [13,74]. Lahive et al. [46] reported significantly greater intrinsic water use efficiency (WUEIntr) in plants grown at elevated CO2 (average of 725 µmol mol−1) and related such an increase to higher PN, as there was no difference in the measured gs between ambient and elevated CO2. In open top chambers, elevated [CO2] up to 700 µmol mol−1 increased PN by 27% and resulted in high cacao biomass accumulation, and thus improved whole plant WUE [47]. Further Hebbar et al. [47] concluded that higher WUE at elevated [CO2] was due to high PN rather than reduced water loss through stomata (E). In the current research with seven contrasting cacao genotypes, increasing [CO2] from 400 to 700 µmol mol−1 significantly increased PN but gs and E were reduced significantly. Based on these findings, it is concluded that increasing PN and decreasing gs and E at elevated [CO2] substantially contributes to the significant increases in WUEInst and WUEIntr [30,46,74]. Enhanced WUEIntr at elevated [CO2] is related to maintenance of higher plant water potential (Ψ) through reduced gs and greater fine root production [43]. Reduced gs in elevated [CO2] may alter plant responses to drought and improve WUE [75].
Irrespective of levels of [CO2], increasing levels of PPFD from 100 to 400 µmol m−2 s−1 increased WUETotal, but there were no changes in WUEInst. Increasing PPFD from 100 to 400 µmol m−2 s−1 slightly reduced WUEIntr from an average of 0.22 to 0.19 µmol CO2 mmol H2O−1. This is a reflection of increases of gs from average of 15.33 to 19.35 mmol H2O m−2 s−1 and moderate increases in PN from average of 2.67 to 3.41 µmol m−2 s−1. In other crops, it has been reported that relationships between WUETotal and WUEInst may be either positive or negative [76]. Increases or decreases in WUE traits with varying PPFD and [CO2] are determined by increases or decreases of PN, gs, and E [4,13,46]. As occurrences of drought episodes are becoming more common in tropical cacao regions [77,78,79], selection of cacao genotypes with high WUE under increasing levels of [CO2] would be beneficial in sustaining yield potential of cacao in current and future drought prone areas.

3.3. Nutrient Use Efficiency Traits

3.3.1. Nutrient Concentrations and Uptake

Cacao genotypes, irrespective of levels of [CO2] and PPFD, showed significant differences in macro–micro nutrient concentrations (Table 3). Overall, LCT EEN 37A, compared to the other genotypes, had the highest concentrations of P, K, Ca, Cu and Fe. The concentrations of P, Ca, Mg and Mn were slightly higher, but concentrations of other macro and micronutrients were comparable to the concentrations reported in the literature [50,80,81]. In all the genotypes tested, irrespective of PPFD, increasing [CO2] from 400 to 700 µmol mol−1 significantly reduced macro–micro nutrient concentrations; however, the effect of increasing [CO2] on Zn concentration was non-significant. This is a reflection of increased dry matter in the shoots (Table 1) of all cacao genotypes with increasing [CO2] which created dilution effects on the nutrient concentrations. The decline in concentrations of all macro–micro nutrients in cacao genotypes with increasing levels of [CO2] differed slightly from the conclusion drawn by Dong et al. [82] from meta-analysis of vegetable crops. They concluded that elevated [CO2] enhanced yield in vegetable crops but decreased the concentration of nitrate, Mg, Fe, and Zn by 18.0, 9.2, 16.0 and 9.4%, respectively, and increased the concentration of Ca by 8.2%. However, the concentration of P, K, S, Cu and Mn in that study were not affected by elevated [CO2]. In Amelonado cacao, Lahive et al. [46] reported that leaf N content decreased at elevated [CO2]. In mango leaves, elevated levels of [CO2] reduced concentrations of several minerals [83]. With the exception of N, Cu and Mn, and irrespective of levels of [CO2], increasing PPFD from 100 to 400 µmol m−2 s−1 reduced concentrations of the other macro and micronutrients. However, the effects were only significant for concentrations of N, K, Ca, Mg and Mn. In several tropical perennial cover crop legumes, increasing [CO2] from 400 to 700 µmol mol−1 slightly decreased all the macro–micro nutrient concentrations. However, increasing PPFD from 100 to 450 µmol m−2 s−1 only slightly decreased concentrations of K, Ca and Fe [62]. In another study with perennial legume cover crops, Baligar et al., [84] reported that increasing PPFD from 200 to 400 µmol m−2 s−1 significantly decreased the concentrations of most of the micronutrients and they attributed this to increased dry matter at the slightly higher PPFD which caused dilution effects.
Uptake of all macro–micro nutrients were significantly influenced by genotypes and Amaz 15 had the highest nutrient uptake (Table 4). Overall, increasing levels of [CO2] from 400 to 700 µmol mol−1 and PPFD from 100 to 400 µmol m−2 s−1 significantly increased uptake of all the macro–micro nutrients. In cacao genotype comum, Baligar et al. [35] reported that increasing [CO2] from 380 to 700 µmol mol−1 increased uptake of all essential nutrients and further stated that such an increase in nutrient uptake at higher [CO2] is due to increased demand for mineral nutrients due to enhanced dry matter accumulation. The overall nutrient accumulation in the current study was in the order of N > Ca >K >Mg > P for macro nutrients and Mn > Zn > Fe > B > Cu for micronutrients.

3.3.2. Nutrient Influx (IN) and Transport (TR)

In most of the cacao growing regions, cacao is often grown in infertile acidic soils and is subjected to the high temperature and radiation common with low soil moisture levels. Such climatic stresses could have major effects on the ability of plants to influx (IN) nutrients from soil through the roots and to transport (TR) these essential nutrients to shoots. In addition to these stresses, increasing atmospheric concentrations of [CO2] could aggravate rates of IN and TR by increasing transpiration losses and photosynthesis. However, very limited information is available on how increasing levels of [CO2] and low to adequate levels of PPFD affect IN and TR of macro–micro nutrients in cacao. In the current study, IN for all macro and micro nutrients were significantly influenced by genotypes, [CO2] and PPFD (Table 5). Irrespective of levels of [CO2] and PPFD, cacao genotype SCA 6 had higher IN of all macro–micro nutrients. Based on these findings SCA 6 could be a superior genotype to use as rootstock in establishing new plantations in infertile soils under changing climatic conditions. In the current study, irrespective of levels of PPFD, IN for all macro–micro nutrients increased significantly by increasing [CO2] from 400 to 700 µmol mol−1. It has been previously reported in cacao genotype comum that increasing [CO2] from 380 to 700 µmol mol−1 tended to increase IN for many of the essential nutrients [35]. In the current study, increasing PPFD from 100 to 400 µmol m−2 s−1 significantly increased IN for all nutrients irrespective of levels of [CO2]. Baligar et al. [35] found a similar result, but also that increases in PPFD to 1050 µmol m−2 s−1 tended to decrease IN for N, K, Ca, Mg, P, S, Cu and Fe. Increased plant influx (IN) of more nutrients from the growth medium helps meet increased demand by increased shoot biomass accumulation.
With the exceptions of K, Ca and Cu, transport (TR) for the other macro–micro nutrients were significantly influenced by cacao genotypes (Table 6). SCA 6 was superior in transport of N, Ca, Fe, and Mn and Coca 3370 was superior in TR for Mg, B and Mn. Overall, with a few exceptions, TR for all the macro–micro nutrients were significantly increased by increasing [CO2] from 400 to 700 µmol mol−1 and PPFD from 100 to 400 µmol m−2 s−1. In cacao genotype comum, Baligar et al. [35] reported that increasing [CO2] from 380 to 700 µmol mol−1 decreased TR of N, Ca, and Zn, and increased TR for other elements. Such variations in IN and TR at varying levels of [CO2] and PPFD could be related to nature of genotypes and their interactions with levels of [CO2] and PPFD.

3.3.3. Nutrient Use Efficiency

With the exception of Mn, all cacao genotypes in this study, irrespective of levels of [CO2] and PPFD, showed significant differences for NUE of all the other essential nutrients (Table 7). The existence of interspecific variations in NUE of macro and micro nutrients have been well documented for field, horticultural and perennial legume crops [62,63,85,86,87,88]. Variations in the growth and uptake and nutrient use efficiency among crop cultivars have been related to absorption, translocation, shoot demand, and dry matter production potentials per unit of nutrient absorbed [85,86]. In agroforestry systems, cacao is grown as an understory plant and subjected to rising [CO2] and low levels of PPFD. Under such situations cacao genotypes that have high nutrient use efficiency for essential nutrients might be able to grow well and produce higher yields. Deficiencies of P, Ca, Mg, Zn and Fe have been widely reported in soils of cacao growing regions of the world [11,48,50]. Cabala-Rosand et al. [50] state that under field conditions the most common deficiencies noted in cacao are N, K, Zn, Fe and B. P is also a limiting nutrient in almost all soils under cacao [49]. Genotypes that have high NUE for any of these nutrients could improve the sustainability and productivity of cacao grown in nutrient deficient soils under agroforestry systems. Amaz 15 was most efficient in NUE for N, K, Ca, B, Cu and Fe and SCA 6 was most efficient for P and K. Since Amaz15 had the longest root length among the cacao genotypes tested, this probably helped it to acquire more nutrients. Barber [89] states that the quantity of a nutrient taken up by a plant depends on the configuration and growth rate of the roots. Irrespective of levels of PPFD, increasing [CO2] from 400 to 700 µmol mol−1 significantly increased NUE for all nutrients. In cacao Comum, Baligar et al. [35] reported that NUE for N, Mg, Cu, Mn and Zn increased with increasing [CO2] from 380 to 700 µmol mol−1. Irrespective of levels of [CO2], increasing PPFD significantly affected NUE for K, Ca, Mg, B and Mn. With the exceptions of N and Fe, increasing levels of PPFD from 100 to 400 µmol m−2 s−1 increased NUE for all other nutrients.

4. Conclusions

Under glasshouse conditions, elevated [CO2] increased growth, physiology, nutrient uptake and use efficiency; however, low light decreased growth, photosynthesis and nutrient uptake of cacao genotypes. Intraspecific differences were found in the genotypes such that AMAZ 15 was the highest for many parameters and LCT EEN 37A was often the lowest. Na 33 had high Fe uptake which could be a problem on Fe limited soils, but further testing is needed. Higher WUE in increasing levels of [CO2] should be considered in selection of cacao genotypes useful for drought prone areas to maintain cacao sustainability and improve yields.

Author Contributions

V.C.B. conceived the study and was in charge of overall direction and planning; M.K.E. carried out the experiment, collected data and performed statistical analysis; A.-A.F.A., Q.R.d.A. and D.A. assisted in selection of cacao genotypes and implementation of the experiment; Z.H. conducted plant analysis and assisted in implementation of the experiment. All authors contributed to writing of the manuscript. All authors have read and agreed to the published version of the manuscript.


This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Relevant data applicable to this research are within the paper.


We thank Regina C. R. Machado and Martin Aitken of MARS Center for Cocoa Research Alimirante, Itajuipe, Bahia, Brazil for providing pods of different cacao genotypes.

Conflicts of Interest

The authors declare no conflict of interest.


  1. Galyuon, I.K.A.; McDavid, C.R.; Lopez, F.B.; Spence, J.A. The effect of irradiance level on cocoa (Theobroma cacao L): I. Growth and leaf adaptations. Trop. Agric. (Trinidad) 1996, 73, 23–28. [Google Scholar]
  2. Serrano, P.; Biehl, B. The effect of light luminous stress on the cocoa plant: Fluorometric measurements under experimental (laboratory) conditions and in the field. In Proceedings of the 12th International Cocoa Research Conference, Salvador, Bahia, Brazil, 17–23 November 1996; pp. 581–588. [Google Scholar]
  3. Mielke, M.S.; De Almeida, A.-A.F.; Gomes, F.P. Photosynthetic traits of five neotropical rainforest tree species: Interactions between light response curves and leaf-to-air vapour pressure deficit. Braz. Arch. Biol. Technol. 2005, 48, 815–824. [Google Scholar] [CrossRef][Green Version]
  4. Daymond, A.J.; Tricker, P.J.; Hadley, P. Genotypic variation in photosynthesis in cacao is correlated with stomatal conductance and leaf nitrogen. Biol. Plant. 2011, 55, 99–104. [Google Scholar] [CrossRef]
  5. Cunningham, R.K.; Burridge, J.C. The Growth of Cacao (Theobroma cacao) With and Without Shade: With one Figure in the Text. Ann. Bot. 1960, 24, 458–462. [Google Scholar] [CrossRef]
  6. Beer, J.; Muschler, R.; Kass, D.; Somarriba, E. Shade management in coffee and cacao plantations. Agrofor. Syst. 1997, 38, 139–164. [Google Scholar] [CrossRef]
  7. Zuidema, P.A.; Leffelaar, P.A.; Gerritsma, W.; Mommer, L.; Anten, N.P. A physiological production model for cocoa (Theobroma cacao): Model presentation, validation and application. Agric. Syst. 2005, 84, 195–225. [Google Scholar] [CrossRef][Green Version]
  8. Gattward, J.N.; Almeida, A.-A.F. Cacao tree responses to variation in water availability. In Cocoa: Cultivation, Research and Innovation; Souza Júnior, J.O., Ed.; EDITUS Pub.: Ilhéus, Brazil, 2018; pp. 59–84. [Google Scholar]
  9. De Almeida, A.-A.F.; Valle, R.R. Ecophysiology of the cacao tree. Braz. J. Plant Physiol. 2007, 19, 425–448. [Google Scholar] [CrossRef][Green Version]
  10. Ahenkorah, Y.; Akrofi, G.S.; Adri, A.K. The end of the first cocoa shade and manurial experiment at the Cocoa Research Institute of Ghana. J. Hortic. Sci. 1974, 49, 43–51. [Google Scholar] [CrossRef]
  11. Willson, K. Coffee, Cocoa and Tea; CABI Publishing: Wallingford, UK, 1999. [Google Scholar]
  12. Wood, G.A.R.; Lass, R.A. Cocoa, 4th ed.; Blackwell Science: Oxford, UK, 2001. [Google Scholar]
  13. 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]
  14. Alvim, P.; de Cacao, T. Ecophysiology of Tropical Crops; de Alvim, P.T., Kozlowski, T.T., Eds.; Academy Press: New York, NY, USA, 1977; pp. 279–313. [Google Scholar] [CrossRef]
  15. Lobão, D.E.; Setenta, W.C.; de Lobão, E.S.P.; Curvelo, K.; Valle, R.R. Cacao cabruca: Sistema agrossilvicultural tropical. In Ciencia, Tecnologia e Manejo do Cacaueiro; Valle, R.R., Ed.; Grafica e Editoria Vital Ltd.: Ilheus, Brazil, 2007; pp. 290–323. [Google Scholar]
  16. Rice, R.A.; Greenberg, R. Cacao Cultivation and the Conservation of Biological Diversity. Ambio 2000, 29, 167–173. [Google Scholar] [CrossRef]
  17. Tscharntke, T.; Clough, Y.; Bhagwat, S.A.; Buchori, D.; Faust, H.; Hertel, D.; Hölscher, D.; Juhrbandt, J.; Kessler, M.; Perfecto, I.; et al. Multifunctional shade-tree management in tropical agroforestry landscapes—A review. J. Appl. Ecol. 2011, 48, 619–629. [Google Scholar] [CrossRef][Green Version]
  18. Sambuichi, R.H.R.; Vidal, D.B.; Piasentin, F.B.; Jardim, J.G.; Viana, T.G.; Menezes, A.A.; Mello, D.L.N.; Ahnert, D.; Baligar, V.C. Cabruca agroforests in southern Bahia, Brazil: Tree component, management practices and tree species conservation. Biodivers. Conserv. 2012, 21, 1055–1077. [Google Scholar] [CrossRef]
  19. Acheampong, K.; Hadley, P.; Daymond, A.J. Photosynthetic activity and early growth of four cacao genotypes as influenced by different shade regimes under west african dry and wet season conditions. Exp. Agric. 2012, 49, 31–42. [Google Scholar] [CrossRef][Green Version]
  20. Saj, S.; Durot, C.; Sakouma, K.M.; Gamo, K.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. Agric. Sustain. 2017, 15, 282–302. [Google Scholar] [CrossRef]
  21. Jagoret, P.; Ngnogue, H.T.; Malézieux, E.; Michel, I. Trajectories of cocoa agroforests and their drivers over time: Lessons from the Cameroonian experience. Eur. J. Agron. 2018, 101, 183–192. [Google Scholar] [CrossRef]
  22. Nijmeijer, A.; Lauri, P.-E.; Harmand, J.-M.; Freschet, G.T.; Nieboukaho, J.-D.E.; Fogang, P.K.; Enock, S.; Saj, S. Long-term dynamics of cocoa agroforestry systems established on lands previously occupied by savannah or forests. Agric. Ecosyst. Environ. 2019, 275, 100–111. [Google Scholar] [CrossRef]
  23. Schroth, G.; Krauss, U.; Gasparotto, L.; Aguilar, J.A.D.; Vohland, K. Pests and diseases in agroforestry systems of the humid tropics. Agrofor. Syst. 2000, 50, 199–241. [Google Scholar] [CrossRef]
  24. Niether, W.; Armengot, L.; Andres, C.; Schneider, M.; Gerold, G. Shade trees and tree pruning alter throughfall and microclimate in cocoa (Theobroma cacao L.) production systems. Ann. For. Sci. 2018, 75, 38. [Google Scholar] [CrossRef][Green Version]
  25. Abdulai, I.; Jassogne, L.; Graefe, S.; Asare, R.; Van Asten, P.; Läderach, P.; Vaast, P. Characterization of cocoa production, income diversification and shade tree management along a climate gradient in Ghana. PLoS ONE 2018, 13, e0195777. [Google Scholar] [CrossRef]
  26. 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]
  27. Raja Harun, R.M.; Kamariah, H.I. The effects of shading regimes on the growth of cocoa Seedlings (Theobroma cacao L.). Pertanika 1983, 6, 1–5. [Google Scholar]
  28. Okali, D.U.U.; Owusu, J.K. Growth analysis and photosynthetic rates of cocoa (Theobroma cacao L.) seedlings in relation to varying shade and nutrient regimes. Ghana J. Agric. Sci. 1975, 8, 51–67. [Google Scholar]
  29. Hartemink, A.E. Nutrient Stocks, Nutrient Cycling, and Soil Changes in Cocoa Ecosystems: A Review. Adv. Agron. 2005, 86, 227–253. [Google Scholar] [CrossRef]
  30. Baligar, V.C.; Bunce, J.A.; Machado, R.C.R.; Elson, M.K. Photosynthetic photon flux density, carbon dioxide concentration, and vapor pressure deficit effects on photosynthesis in cacao seedlings. Photosynthetica 2008, 46, 216–221. [Google Scholar] [CrossRef]
  31. Bastide, P.; Jimmy, I. Gas transfer measurements on young cocoa trees in field and modeling of photosynthetic activity. In Proceedings of the 14th International Cocoa Research Conference, Accra, Ghana, 13–18 October 2003; pp. 195–203. [Google Scholar]
  32. Hutcheon, W.V. Photosynthesis of cocoa: Photosynthesis in relation to the light and plant nutrient status. In Report Cocoa Res. Inst. Ghana, 1973–1974; 1976; pp. 186–188. [Google Scholar]
  33. Raja Harun, R.M.; Hardwick, K. The effects of prolonged exposure to different light intensities on the photosynthesis of cocoa leaves. In Proceedings of the 10th International Cocoa Research Conference, Santo Domingo, Dominican Republic, 17–23 May 1987; pp. 205–209. [Google Scholar]
  34. Miyaji, K.-I.; Da Silva, W.S.; Alvim, P.D.T. Longevity of leaves of a tropical tree, Theobroma cacao, grown under shading, in relation to position within the canopy and time of emergence. New Phytol. 1997, 135, 445–454. [Google Scholar] [CrossRef][Green Version]
  35. Baligar, V.C.; Bunce, J.A.; Bailey, B.A.; Machado, R.C.; Pomella, A.W.V. Carbon dioxide and photosynthetic photon flux density effects on growth and mineral uptake of cacao. J. Food Agric. Environ. 2005, 3, 142–147. [Google Scholar] [CrossRef]
  36. Gommers, C.M.; Visser, E.J.; Onge, K.R.S.; Voesenek, L.A.; Pierik, R. Shade tolerance: When growing tall is not an option. Trends Plant Sci. 2013, 18, 65–71. [Google Scholar] [CrossRef] [PubMed]
  37. Fiorucci, A.-S.; Fankhauser, C. Plant Strategies for Enhancing Access to Sunlight. Curr. Biol. 2017, 27, R931–R940. [Google Scholar] [CrossRef][Green Version]
  38. Van Vuuren, D.P.; Edmonds, J.; Kainuma, M.; Riahi, K.; Thomson, A.; Hibbard, K.; Hurtt, G.C.; Kram, T.; Krey, V.; Lamarque, J.-F.; et al. The representative concentration pathways: An overview. Clim. Chang. 2011, 109, 5–31. [Google Scholar] [CrossRef]
  39. IPCC. Climate Change 2014: Synthesis Report. In Contribution of Working Groups I, II and III 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]
  40. Amthor, J.S. Terrestrial higher-plant response to increasing atmospheric [CO2] in relation to the global carbon cycle. Glob. Chang. Biol. 1995, 1, 243–274. [Google Scholar] [CrossRef]
  41. Galyuon, I.K.A.; McDavid, C.R.; Lopez, F.B.; Spence, J.A. The effect of irradiance level on cocoa (Theobroma cacao L): II. Gas exchange and chlorophyll fluorescence. Trop. Agric. (Trinidad) 1996, 73, 29–33. [Google Scholar]
  42. Miyaji, K.-I.; Da Silva, W.S.; Alvim, P.D.T. Productivity of leaves of a tropical tree, Theobroma cacao, grown under shading, in relation to leaf age and light conditions within the canopy. New Phytol. 1997, 137, 463–472. [Google Scholar] [CrossRef][Green Version]
  43. Wullschleger, S.D.; Gunderson, C.A.; Hanson, P.J.; Wilson, K.B.; Norby, R.J. Sensitivity of stomatal and canopy conductance to elevated CO2 concentration—Interacting variables and perspectives of scale. New Phytol. 2002, 153, 485–496. [Google Scholar] [CrossRef]
  44. Long, S.P.; Ainsworth, E.A.; Rogers, A.; Ort, D.R. Rising atmospheric carbon dioxide: Plants face the Future. Annu. Rev. Plant Biol. 2004, 55, 591–628. [Google Scholar] [CrossRef] [PubMed]
  45. Branco, M.C.D.S.; Baligar, V.C.; De Almeida, A.-A.F.; Dalmolin, Â.C.; Ahnert, D. Influence of low light intensity and soil flooding on cacao physiology. Sci. Hortic. 2017, 217, 243–257. [Google Scholar] [CrossRef]
  46. Lahive, F.; Hadley, P.; Daymond, A.J. The impact of elevated CO2 and water deficit stress on growth and photosynthesis of juvenile cacao (Theobroma cacao L.). Photosynthetica 2017, 56, 911–920. [Google Scholar] [CrossRef][Green Version]
  47. Hebbar, K.B.; Apshara, E.; Chandran, K.P.; Prasad, P.V.V. Effect of elevated CO2, high temperature, and water deficit on growth, photosynthesis, and whole plant water use efficiency of cocoa (Theobroma cacao L.). Int. J. Biometeorol. 2020, 64, 47–57. [Google Scholar] [CrossRef] [PubMed]
  48. Cunningham, R.K. Micro-nutrient deficiency in cacao in Ghana. Emp. J. Exp. Agric. 1964, 32, 42–50. [Google Scholar]
  49. Ahenkorah, Y. Influence of environment on growth and production of the cacao tree: Soils and nutrition. In Proceeding of the 7th International Cocoa Research Conference, Douala, Cameroon, 4–12 November 1979; pp. 167–176. [Google Scholar]
  50. Cabala-Rosand, P.; Santana, M.B.M.; de Santana, C.J.L. Cacao. In Detecting Mineral Nutrient Deficiencies in Tropical and Temperate Crops; Plucknett, D.L., Sprague, H.B., Eds.; Westview Tropical Agriculture Series; Westview Press: Boulder, CO, USA, 1989; pp. 409–425. [Google Scholar]
  51. Clark, R.B.; Baligar, V.C. Acidic and alkaline soil constraints in plant mineral nutrition. In Plant Environment Interactions II; Wilkinson, R.E., Ed.; Marcel Dekker Publ.: New York, NY, USA, 2000; pp. 133–177. [Google Scholar]
  52. Hartemink, A.E. Soil Fertility Decline in the Tropics: With Case Studies on Plantations; CABI Publishing: Wallingford, UK, 2003. [Google Scholar] [CrossRef]
  53. Yapp, J.H.H.; Hadley, P. Inter-relationships between canopy architecture, light interception, vigor and yield in cocoa: Implications for improving production efficiency. In Proceedings of the International Cocoa Conference: Challenges in the 90′s, Kuala Lumpur, Malaysia, 25–28 September 1991; Malaysian Cocoa Board: Kuala Lumpur, Malaysia, 1994; pp. 332–350. [Google Scholar]
  54. Motamayor, J.C.; Lachenaud, P.; Mota, J.W.D.S.E.; Loor, R.; Kuhn, D.N.; Brown, J.S.; Schnell, R.J. Geographic and Genetic Population Differentiation of the Amazonian Chocolate Tree (Theobroma cacao L.). PLoS ONE 2008, 3, e3311. [Google Scholar] [CrossRef] [PubMed][Green Version]
  55. Daymond, A.J.; Hadley, P.; Machado, R.C.R.; Ng, E. Canopy characteristics of contrasting clones of cacao (theobroma cacao). Exp. Agric. 2002, 38, 359–367. [Google Scholar] [CrossRef]
  56. Bartley, B.G.D. The Genetic Diversity of Cacao and its Utilization; CABI Publishing: Wallingford, UK, 2005. [Google Scholar]
  57. Turnbull, C.J.; Hadley, P. International Cocoa Germplasm Database (ICGD); CRA Ltd./ICE Futures Europe/University of Reading: Reading, UK, 2015; Available online: (accessed on 22 May 2020).
  58. Ahnert, D.; Eskes, A.B. Developments in cacao breeding programmes in Africa and the Americas. In Achieving Sustainable Cultivation of Cocoa; Umaharan, P., Ed.; Burleigh Dodds Science Publishing: Cambridge, UK, 2018; pp. 1–40. [Google Scholar] [CrossRef]
  59. USEPA. Method 200.7, Rev. 5.0, Trace Elements in Water, Solids, and Biosolids by Inductively Coupled Plasma-Atomic Emission Spectrometry; USEPA, Office of Science and Technology: Washington, DC, USA, 2001. [Google Scholar]
  60. Bremner, J.M. Nitrogen Total. In Methods of Soil Analysis, Part 3 Chemical Methods; Sparks, D.L., Ed.; SSSA: Madison, WI, USA, 1996; pp. 1085–1122. [Google Scholar] [CrossRef]
  61. De Araújo, R.P.; De Almeida, A.-A.F.; Barroso, J.P.; De Oliveira, R.A.; Gomes, F.P.; Ahnert, D.; Baligar, V. Molecular and morphophysiological responses cocoa leaves with different concentrations of anthocyanin to variations in light levels. Sci. Hortic. 2017, 224, 188–197. [Google Scholar] [CrossRef][Green Version]
  62. Baligar, V.C.; Elson, M.; He, Z.L.; Li, Y.; Paiva, A.D.Q.; Ahnert, D.; Almeida, A.-A.F.; Fageria, N.K. Ambient and Elevated Carbon Dioxide on Growth, Physiological and Nutrient Uptake Parameters of Perennial Leguminous Cover Crops under Low Light Intensities. Int. J. Plant Soil Sci. 2017, 15, 1–16. [Google Scholar] [CrossRef]
  63. Baligar, V.C.; Elson, M.K.; He, Z.L.; Li, Y.; Paiva, A.D.Q.; Ahnert, D.; Almeida, A.-A.F. Growth, Physiological and Nutrient Uptake Traits of Crotalaria Cover Crops Influenced by Levels of Carbon Dioxide under Low Light Intensities. Int. J. Plant Soil Sci. 2018, 23, 1–14. [Google Scholar] [CrossRef]
  64. Hollinger, D.Y. Gas exchange and dry matter allocation responses to elevation of atmospheric CO2 concentration in seedlings of three tree species. Tree Physiol. 1987, 3, 193–202. [Google Scholar] [CrossRef][Green Version]
  65. Poorter, H. Interspecific variation in the growth response of plants to an elevated ambient CO2 concentration. Vegetatio 1993, 104, 77–97. [Google Scholar] [CrossRef]
  66. Bunce, J. Variation in growth stimulation by elevated carbon dioxide in seedlings of some C3 crop and weed species. Glob. Chang. Biol. 1997, 3, 61–66. [Google Scholar] [CrossRef][Green Version]
  67. Sefcik, L.T.; Zak, D.R.; Ellsworth, D.S. Photosynthetic responses to understory shade and elevated carbon dioxide concentration in four northern hardwood tree species. Tree Physiol. 2006, 26, 1589–1599. [Google Scholar] [CrossRef] [PubMed][Green Version]
  68. Ellsworth, D.S.; Thomas, R.; Crous, K.Y.; Palmroth, S.; Ward, E.; Maier, C.; DeLucia, E.; Oren, R. Elevated CO2 affects photosynthetic responses in canopy pine and subcanopy deciduous trees over 10 years: A synthesis from Duke FACE. Glob. Chang. Biol. 2011, 18, 223–242. [Google Scholar] [CrossRef]
  69. Cure, J.D.; Acock, B. Crop responses to carbon dioxide doubling: A literature survey. Agric. For. Meteorol. 1986, 38, 127–145. [Google Scholar] [CrossRef]
  70. Kimball, B.; Kobayashi, K.; Bindi, M. Responses of Agricultural Crops to Free-Air CO2 Enrichment. Adv. Agron. 2002, 77, 293–368. [Google Scholar] [CrossRef]
  71. Yan, W.; Zhong, Y.; Shangguan, Z. A meta-analysis of leaf gas exchange and water status responses to drought. Sci. Rep. 2016, 6, 20917. [Google Scholar] [CrossRef] [PubMed][Green Version]
  72. Prior, S.A.; Runion, G.B.; Marble, S.C.; Rogers, H.H.; Gilliam, C.H.; Torbert, H.A. A Review of Elevated Atmospheric CO2 Effects on Plant Growth and Water Relations: Implications for Horticulture. HortScience 2011, 46, 158–162. [Google Scholar] [CrossRef][Green Version]
  73. Schneider, M.; Andres, C.; Trujillo, G.; Alcon, F.; Amurrios, P.; Perez, E.; Weibel, F.; Milz, J. Cocoa and total system yields of organic and conventional agroforestry vs. monoculture systems in a long-term field trial in Bolivia. Exp. Agric. 2016, 53, 351–374. [Google Scholar] [CrossRef][Green Version]
  74. Ainsworth, E.A.; Long, S.P. What have we learned from 15 years of free-air CO2 enrichment (FACE)? A meta-analytic review of the responses of photosynthesis, canopy properties and plant production to rising CO2. New Phytol. 2004, 165, 351–372. [Google Scholar] [CrossRef]
  75. Eamus, D. The interaction of rising CO2 and temperatures with water use efficiency. Plant Cell Environ. 1991, 14, 843–852. [Google Scholar] [CrossRef]
  76. Medrano, H.; Tomás, M.; Martorell, S.; Flexas, J.; Hernández, E.; Rosselló, J.; Pou, A.; Escalona, J.-M.; Bota, J. From leaf to whole-plant water use efficiency (WUE) in complex canopies: Limitations of leaf WUE as a selection target. Crop. J. 2015, 3, 220–228. [Google Scholar] [CrossRef][Green Version]
  77. Laderach, P.; Eitzinger, A.; Martinez, A.; Castro, N. Predicting the Impact of Climate Change on the Cocoa-Growing Regions in Ghana and Cote d’Ivoire; CIAT: Managua, Nicaragua, 2011; Available online: (accessed on 6 November 2020).
  78. Schroth, G.; Läderach, P.; Martinez-Valle, A.I.; Bunn, C.; Jassogne, L. Vulnerability to climate change of cocoa in West Africa: Patterns, opportunities and limits to adaptation. Sci. Total. Environ. 2016, 556, 231–241. [Google Scholar] [CrossRef] [PubMed][Green Version]
  79. Gateau-Rey, L.; Tanner, E.V.J.; Rapidel, B.; Marelli, J.-P.; Royaert, S. Climate change could threaten cocoa production: Effects of 2015-16 El Niño-related drought on cocoa agroforests in Bahia, Brazil. PLoS ONE 2018, 13, e0200454. [Google Scholar] [CrossRef] [PubMed]
  80. Snoeck, J. Cacao. In Plant Analysis as a Guide to the Nutrient Requirements of Temperate and Tropical Crops; Martin-Prevel, P., Gagnard, J., Gautier, P., Jones, J.B., Jr., Holmes, M.R.J., Eds.; Lavoisier: New York, NY, USA, 1984; pp. 432–439. [Google Scholar]
  81. Bhargava, B.S.; Raghupathi, H. Analysis of plant materials for macro and micronutrients. In Methods of Analysis of Soils, Plants, Waters and Fertilisers; Tandon, H.L.S., Ed.; FDCO: New Delhi, India, 1993; pp. 49–82. [Google Scholar]
  82. Dong, J.; Gruda, N.; Lam, S.K.; Li, X.; Duan, Z. Effects of Elevated CO2 on Nutritional Quality of Vegetables: A Review. Front. Plant Sci. 2018, 9, 924. [Google Scholar] [CrossRef]
  83. Schaffer, B.; Whiley, A.W.; Searle, C.; Nissen, R.J. Leaf Gas Exchange, Dry Matter Partitioning, and Mineral Element Concentrations in Mango as Influenced by Elevated Atmospheric Carbon Dioxide and Root Restriction. J. Am. Soc. Hortic. Sci. 1997, 122, 849–855. [Google Scholar] [CrossRef][Green Version]
  84. Baligar, V.C.; Fageria, N.K.; Paiva, A.Q.; Silveira, A.; Pomella, A.W.V.; Machado, R.C.R. Light Intensity Effects on Growth and Micronutrient Uptake by Tropical Legume Cover Crops. J. Plant Nutr. 2006, 29, 1959–1974. [Google Scholar] [CrossRef]
  85. Gerloff, G.C.; Gabelman, W.H. Genetic basis of inorganic plant nutrition. In Inorganic Plant Nutrition; Lauchli, A., Bielski, R.L., Eds.; Springer: New York, NY, USA, 1983; pp. 453–480. [Google Scholar]
  86. Vose, P.B. Effects of genetic factors on nutritional requirements of plants. In Crop Breeding: A Contemporary Basis; Vose, P.B., Blixt, S.G., Eds.; Pergamon Press: Oxford, UK, 1984; pp. 67–114. [Google Scholar] [CrossRef]
  87. Baligar, V.C.; Duncan, R.R. (Eds.) Crops as Enhancers of Nutrient Use; Academic Press: San Diego, CA, USA, 1990. [Google Scholar]
  88. Baligar, V.C.; Fageria, N.K.; He, Z.L. Nutrient Use Efficiency in Plants. Commun. Soil Sci. Plant Anal. 2001, 32, 921–950. [Google Scholar] [CrossRef]
  89. Barber, S.A. Soil Nutrient Bioavailability: A Mechanistic Approach; John Wiley & Sons: New York, NY, USA, 1995. [Google Scholar]
Table 1. The effect of [CO2] and photosynthetic photon flux density (PPFD) on shoot and root growth, leaf growth, relative growth rate (RGR) and net assimilation rate (NAR) of seven cacao genotypes.
Table 1. The effect of [CO2] and photosynthetic photon flux density (PPFD) on shoot and root growth, leaf growth, relative growth rate (RGR) and net assimilation rate (NAR) of seven cacao genotypes.
CO2 (µmol mol−1)PPFD
(µmol m−2 s−1)
Total Dry Weight (g/plant)Root Dry Weight (g/plant)Root/
Stem Height (cm/plant)Total Root Length (cm/plant)Leaf Area
Specific Leaf
(cm2 g−1)
(g g−1 d−1)
(× 10−2)
(g cm−2 d−1)
(× 10−4)
Coca 3370
CCN 51
Amaz 15
Na 33
Genotype (G)******************
[CO2] (C)****NS************
PPFD (P)****NS***********
*, ** Significant at 0.05 and 0.01 levels of probability, respectively. NS = Not significant.
Table 2. The effect of [CO2] and photosynthetic photon flux density (PPFD) on photosynthesis and its components, and water use efficiency of seven cacao genotypes.
Table 2. The effect of [CO2] and photosynthetic photon flux density (PPFD) on photosynthesis and its components, and water use efficiency of seven cacao genotypes.
CO2 (µmol mol−1)PPFD
(µmol m−2 s−1)
SPAD IndexPhotosynthesis
(µmol CO2 m−2 s−1)
Stomatal Conductance (mmol H2O m−2 s−1)Internal CO2 (µmol mol−1) Transpiration (mmol H2O m−2 s−1)WUETotal
(g shoot/g trans.) (×10−3)
WUEInst ¥ (µmol CO2/mmol H2O)WUEIntr ¥ (µmol CO2/mmol H2O)
40010042.32.6420.66157.60.291 8.34 9.170.132
20042.81.7515.36158.30.213 6.22 8.710.125
40042.43.0225.02222.80.34123.80 8.900.126
Coca 3370
40010043.83.2120.19106.40.284 9.5311.510.163
20040.22.1715.88128.30.218 5.51 9.850.140
40040.23.2724.96127.10.321 7.3410.020.133
CCN 51
40010042.12.1918.02236.60.26712.29 9.470.146
20042.91.8512.58132.90.179 5.26 9.640.139
40039.41.8020.13351.20.285 5.91 5.960.085
70010042.22.52 8.47189.30.12915.6119.580.296
Amaz 15
20040.32.9017.77 81.10.238 6.1212.220.166
40039.53.4422.41132.30.308 7.3311.190.154
40010043.53.5742.11323.70.552 5.57 7.760.106
40038.84.1631.75190.00.422 6.09 9.990.135
Na 33
20038.62.1413.86109.60.196 5.3610.790.158
40036.91.1111.83233.20.172 4.29 8.440.118
70010036.12.03 7.64261.10.11620.6615.070.234
20042.31.94 7.15142.50.105 8.9020.790.310
40010044.81.5110.70153.60.157 9.25 9.320.136
20042.61.7713.65150.20.194 8.32 9.080.130
40043.72.9226.40177.20.334 6.07 8.740.113
70010043.31.39 4.73235.90.07318.8519.170.320
20041.72.41 9.35239.70.13212.8317.480.249
Genotype (G)*****NS**NSNSNS
[CO2] (C)NS****NS********
*, ** Significant at 0.05 and 0.01 levels of probability, respectively. NS = Not significant. ¥ Instantaneous water use efficiency, WUEInst = PN/E, (µmol CO2/mmol H2O); Intrinsic water use efficiency, WUEIntr = PN/gs, (µmol CO2/mmol H2O).
Table 3. The effect of [CO2] and photosynthetic photon flux density (PPFD) on macro–micro nutrient concentrations of seven cacao genotypes.
Table 3. The effect of [CO2] and photosynthetic photon flux density (PPFD) on macro–micro nutrient concentrations of seven cacao genotypes.
CO2 (µmol mol−1)PPFD
(µmol m−2 s−1)
mg g−1µg g−1
40010027.314.4815.4015.876.8034.3024.15 61.90 77.5440.83
20028.924.2614.5315.796.7734.8322.47 57.63 62.9136.75
40031.465.0415.5415.366.3432.6824.88 95.58 55.7251.21
70010025.844.0015.8214.866.2628.3818.81 25.66 63.1033.31
20024.153.6514.0313.816.5723.8618.14 18.00 49.4634.98
40026.973.7112.9912.945.5724.5417.11 19.54 44.6836.48
Coca 3370
40010027.003.8214.7014.828.0430.7621.11 56.73110.0658.68
20025.464.0215.0215.138.3533.5119.90 54.62 73.6040.85
40028.153.9112.8314.097.5029.2821.21 72.55 63.1041.48
70010026.214.1512.9213.957.0324.2017.39 18.73 67.5041.66
20025.154.4513.2213.717.8924.3218.87 21.72 61.3448.28
40024.543.8511.2311.846.2019.3217.27 34.04 36.6746.01
CCN 51
40010028.854.3313.6414.356.3930.2923.14 60.94 74.3854.68
20027.684.4714.8215.647.2430.7722.56 44.73 66.9547.11
40029.714.2014.9414.036.2527.0525.80 52.43 43.8641.47
70010024.944.3313.9316.486.8024.9421.98 21.77 79.6576.98
20024.693.6312.8013.896.5320.5317.58 26.86 54.5450.82
40024.913.7311.4813.566.3423.8219.11 40.12 47.7454.03
Amaz 15
40010024.834.1513.4913.626.9426.6617.35 45.41 68.3746.03
20025.174.2814.4515.577.8231.2719.75 43.78 61.2249.74
40025.523.6911.9213.706.7329.1419.65 31.74 47.8471.18
70010023.314.1413.1914.267.5523.5616.61 14.38 68.1745.67
20022.023.7711.2912.046.7419.0714.54 20.07 47.7543.13
40021.733.4810.2211.245.9819.4414.73 15.46 47.1340.99
40010026.704.5717.7316.846.7630.6124.52 77.09 74.4557.56
20030.725.1316.9116.167.8332.8541.88108.84 59.4658.52
40032.584.7515.9815.257.4331.7936.45 80.44 45.7945.27
70010022.394.0614.2713.666.4122.3916.83 30.97 56.9047.76
20024.373.5713.5813.465.7920.6215.62 36.18 54.5348.44
40023.394.1411.4614.546.6220.4717.68 46.68 42.6845.84
Na 33
40010023.113.8113.7915.876.1631.0520.51 67.26 85.8966.47
20026.133.9513.2817.776.6234.3722.94 83.68 64.5161.70
40028.703.6814.5114.486.0834.7021.31 87.95 46.1360.22
70010023.843.7115.0516.806.5030.0218.35 53.72 63.8951.03
20022.353.5911.1914.745.8717.4917.79 44.94 51.6349.01
40020.853.5810.4712.875.7621.7917.81 47.56 39.9063.92
40010024.713.4013.5113.696.2829.4416.05 57.65 75.1744.33
20025.533.4014.0415.536.9331.2419.76 82.19 69.8062.89
40028.233.6513.0213.916.5333.4423.59 95.41 62.9243.49
70010022.083.3013.5514.416.3322.2915.78 32.26 67.8146.56
20022.212.9210.2211.885.4618.7914.00 34.43 50.4836.46
40023.313.6011.4413.366.1923.6717.57 50.73 45.2855.06
Genotype (G)******************
[CO2] (C)******************NS
*, ** Significant at 0.05 and 0.01 levels of probability, respectively. NS = Not significant.
Table 4. The effect of [CO2] and photosynthetic photon flux density (PPFD) on macro–micro nutrient uptake of seven cacao genotypes.
Table 4. The effect of [CO2] and photosynthetic photon flux density (PPFD) on macro–micro nutrient uptake of seven cacao genotypes.
CO2 (µmol mol−1)PPFD
(µmol m−2 s−1)
400100181.929.68101.9105.4 45.18229.1161.1 417.9 513.7 273.3
200193.728.33 98.1106.0 45.69235.3150.1 380.1 416.4 252.7
400178.428.59 88.0 87.1 35.96185.3140.9 541.6 315.6 290.3
700100273.842.21167.2157.5 66.29299.2198.9 287.3 664.8 354.4
200305.345.46169.9169.9 81.61301.8222.3 215.9 608.9 456.2
400317.743.79152.9153.4 66.65295.7203.5 243.8 523.8 446.5
Coca 3370
400100168.623.64 91.5 92.8 50.79193.5133.2 365.3 695.8 363.9
200236.437.28140.2140.5 77.85311.6184.8 499.3 683.4 379.0
400326.945.56148.2164.7 87.26337.9245.5 855.8 738.7 484.3
700100290.446.02143.8153.7 77.97268.9192.3 195.4 759.5 462.4
200427.674.69223.3229.9134.66411.3318.5 419.41055.5 840.9
400447.970.49208.1214.7115.23353.7323.4 607.4 675.6 889.6
CCN 51
400100137.820.65 64.2 69.0 30.70150.6115.1 322.4 349.0 257.9
200196.831.84105.0111.4 51.50217.9161.0 320.8 475.9 334.3
400238.333.56121.7111.7 50.47217.1202.1 390.3 343.9 331.2
700100295.551.38166.1197.0 81.72295.0262.4 262.6 929.6 874.9
200360.752.37185.6200.9 95.23299.6257.3 401.6 803.5 734.4
400521.579.71240.4285.4136.42515.1405.8 888.11036.31150.2
Amaz 15
400100184.530.67100.1100.9 51.36195.8128.5 342.4 504.5 342.4
200254.842.82143.8157.2 78.54311.4195.6 446.2 614.6 502.8
400234.834.19109.6126.6 62.87243.6179.8 320.3 444.5 705.7
700100399.371.40226.4245.4130.08406.2286.9 247.01174.0 785.6
200459.979.81234.8252.1142.20404.9304.8 418.9 998.8 880.4
400509.181.96239.9264.1140.27454.1344.7 366.81111.3 983.2
400100 82.113.38 51.5 51.2 20.41 90.4 69.5 216.3 231.3 162.5
200137.723.46 76.2 71.5 34.44144.9193.9 491.6 249.9 264.4
400118.918.20 60.2 56.7 26.58123.8121.0 276.5 186.0 173.9
700100311.956.55198.8189.9 89.18310.3233.7 429.1 792.1 664.2
200346.050.47188.8189.2 82.05288.0223.7 524.1 767.6 684.7
400387.468.72189.4239.2110.06337.8287.8 743.6 703.7 777.9
Na 33
400100149.224.50 88.9102.3 40.04202.4132.8 410.2 576.1 424.9
200213.532.14108.9146.0 54.84282.9183.9 650.1 541.4 495.1
400140.918.42 73.6 72.3 30.73172.5103.5 361.6 229.7 293.7
700100193.629.74120.4135.2 52.68241.4147.2 425.7 524.4 411.3
200411.166.21207.1269.6109.15326.9321.6 773.0 974.4 920.9
400443.276.07222.4272.1122.75462.6375.51005.5 842.91436.6
400100149.220.43 81.69 82.63 37.87177.2 96.8 348.3 454.9 266.6
200151.220.28 83.63 93.33 41.69190.1118.1 496.9 423.0 366.7
400232.630.07108.20114.97 54.32280.7188.7 707.4 515.0 355.8
700100279.741.96171.99183.14 80.41282.5201.2 407.8 864.1 593.8
200352.345.76162.28187.20 86.23296.9221.0 556.5 799.7 582.1
400453.270.70224.24261.73122.61465.4342.11017.3 916.01091.9
Genotype (G)********************
[CO2] (C)**************NS****
PPFD (P)****************NS**
*, ** Significant at 0.05 and 0.01 levels of probability, respectively. NS = Not significant.
Table 5. The effect of [CO2] and photosynthetic photon flux density (PPFD) on macro–micro influx by root length of seven cacao genotypes.
Table 5. The effect of [CO2] and photosynthetic photon flux density (PPFD) on macro–micro influx by root length of seven cacao genotypes.
CO2 (µmol mol−1)PPFD (µmol m−2 s−1)NPKCaMgBCuFeMnZn
pmol cm root−1 s−1pmol cm root−1 s−1 (×10−3)
Coca 3370
CCN 51
Amaz 15
Na 33
Genotype (G)********************
[CO2] (C)**************NS****
PPFD (P)****NS***********
*, ** Significant at 0.05 and 0.01 levels of probability, respectively. NS = Not significant.
Table 6. The effect of [CO2] and photosynthetic photon flux density (PPFD) on macro–micro nutrient transport of seven cacao genotypes.
Table 6. The effect of [CO2] and photosynthetic photon flux density (PPFD) on macro–micro nutrient transport of seven cacao genotypes.
CO2 (µmol mol−1)PPFD (µmol m−2 s−1)NPKCaMgBCuFeMnZn
pmol g shoot−1 s−1
400768.453.95131.6138.1 89.7
700100826.256.80180.9170.9116.6 1.18
Coca 3370
700100751.553.14131.9146.1118.2 0.910.110.140.510.25
400810.357.00132.3140.4119.7 0.830.130.290.310.33
CCN 51
400100633.639.88101.4121.1 84.2 0.880.110.390.450.25
400831.851.00147.8142.9102.5 0.970.150.380.320.24
200822.153.56151.8166.1127.0 0.880.130.230.470.36
Amaz 15
400100684.551.47134.6138.2113.5 0.970.110.330.510.27
200797.461.40145.9155.6142.8 0.900.120.190.450.33
400812.058.31136.2149.5129.9 0.940.120.150.460.33
400100490.235.11118.7124.9 77.0 0.780.100.410.390.22
400662.541.56116.6119.5 90.2 0.890.160.440.250.19
200835.554.32165.6165.3115.8 0.920.120.320.480.36
400838.266.65146.2186.3138.9 0.960.140.430.390.35
Na 33
400100573.341.70121.1146.7 90.7
400640.135.01113.5120.4 79.8
200824.959.38147.3193.2126.3 0.840.140.420.490.39
400869.749.20141.9154.5117.4 1.360.160.750.500.28
200837.148.70136.3158.5119.0 0.910.120.33 0.490.29
Genotype (G)***NSNS***NS******
[CO2] (C)***********NS**NS**
PPFD (P)*******NS**NS**NS
*, ** Significant at 0.05 and 0.01 levels of probability, respectively. NS = Not significant.
Table 7. The effect of [CO2] and photosynthetic photon flux density (PPFD) on macro–micro nutrient use efficiency (NUE) of seven cacao genotypes.
Table 7. The effect of [CO2] and photosynthetic photon flux density (PPFD) on macro–micro nutrient use efficiency (NUE) of seven cacao genotypes.
CO2 (µmol mol−1)PPFD (µmol m−2 s−1)NPKCaMgBCuFeMnZn
mg shoot mg element−1mg shoot mg element−1 (×104)
70010038.72251.663.67 67.89161.83.605.395.611.623.02
20041.53278.175.12 74.38154.94.205.685.952.072.87
40037.31272.177.24 78.29181.14.105.887.152.252.79
Coca 3370
70010038.28241.477.91 72.07142.44.155.751.221.562.42
20040.30231.377.07 74.78128.04.205.395.521.642.10
40041.19261.889.69 86.28162.75.225.793.042.742.20
CCN 51
70010040.10231.972.30 60.80147.94.024.615.901.281.38
20040.63276.578.26 72.04153.44.895.693.771.841.99
40040.44268.587.37 74.67159.64.375.272.582.131.86
Amaz 15
40039.24274.683.9573.26148.73.625.103.41 2.091.52
70010043.18248.575.97 71.01135.04.436.236.981.492.33
20045.43267.488.61 83.42149.55.306.885.512.092.49
40046.58287.798.15 89.34168.25.316.846.512.122.60
Na 33
70010045.30306.8 74.1169.89158.74.496.473.561.492.22
Genotype (G)***************NS**
[CO2] (C)*******************
*, ** Significant at 0.05 and 0.01 levels of probability, respectively. NS = Not significant.
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Baligar, V.C.; Elson, M.K.; Almeida, A.-A.F.; de Araujo, Q.R.; Ahnert, D.; He, Z. The Impact of Carbon Dioxide Concentrations and Low to Adequate Photosynthetic Photon Flux Density on Growth, Physiology and Nutrient Use Efficiency of Juvenile Cacao Genotypes. Agronomy 2021, 11, 397.

AMA Style

Baligar VC, Elson MK, Almeida A-AF, de Araujo QR, Ahnert D, He Z. The Impact of Carbon Dioxide Concentrations and Low to Adequate Photosynthetic Photon Flux Density on Growth, Physiology and Nutrient Use Efficiency of Juvenile Cacao Genotypes. Agronomy. 2021; 11(2):397.

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Baligar, Virupax C., Marshall K. Elson, Alex-Alan F. Almeida, Quintino R. de Araujo, Dario Ahnert, and Zhenli He. 2021. "The Impact of Carbon Dioxide Concentrations and Low to Adequate Photosynthetic Photon Flux Density on Growth, Physiology and Nutrient Use Efficiency of Juvenile Cacao Genotypes" Agronomy 11, no. 2: 397.

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