Volume 29, 2022
Palm and palm oil / Palmier et huile de palme
Numéro d'article 31
Nombre de pages 11
Section Agronomy
Publié en ligne 10 août 2022

© O.S. Dassou et al., Published by EDP Sciences, 2022

Licence Creative CommonsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


  • Oil palm progenies’ growth characteristics are determined by their genetic backgrounds.

  • K is the main mineral involved in oil palm morphological growth in the Nigerian environment.

  • Mg does not have an effect on the tested progenies’ growth characteristics.

1 Introduction

Oil palm (Elaeis guineensis Jacq.) is the main supplier of vegetal oil in the world (USDA, 2020). Oil palm produces an average yield about 3.8 t ha−1 y−1 of oil, which is six to nine times higher than the yield of other oilseed crops (Skurtis et al., 2010). Oil palm productivity has been continuously improved (Durand-Gasselin et al., 2000; Rival and Levang, 2010) by crossing different oil palm genotypes with useful traits such as fresh fruit bunch (FFB) yield, mesocarp thickness and consequently shell thinness (Cochard et al., 2001; Durand-Gasselin et al., 2006; Durand-Gasselin et al., 2011; Junaidah et al., 2011; Corley and Tinker, 2016). Oil productivity over the lifespan of the oil palm is determined using several different factors, among which researchers have focused particularly on slow trunk growth rates to extend the economic life of the palm (Baudouin et al., 1997; Tailliez and Koffi, 1992; Durand-Gasselin et al., 2009; Verheye, 2010; Bonneau et al., 2014; Bonneau et al., 2017; Konan et al., 2014; Fan et al., 2015; Corley and Tinker, 2016). The trunk growth rate varies between 25 and 65 cm per year (Cochard et al., 2001; Konan et al., 2014), depending on environmental and genetic factors (Cochard et al., 2005; Verheye, 2010). It has been shown that growth characteristics vary according to oil palm genetic origins (Nouy et al., 1999; Konan et al., 2014; Corley and Tinker, 2016). We consequently assumed that this would also be the case for four selected progenies with different genetic backgrounds ( Tab. 1). However, growth characteristics are also essential parameters to assess palm trees’ mineral uptake and use (Goh et al., 1999; Marschner et al., 2007; Prabowo et al., 2012). In an earlier study conducted in Indonesia on the same progenies, it has been shown that their leaflet K and Mg concentrations vary significantly from one to another, after having received equal amounts of fertilizers (Ollivier et al., 2017). These minerals (K and Mg) play diverse roles in palm growth and development and have a number of physiological and enzymatic functions: K is a crucial element that directly affects photosynthesis and gas exchange (Legros et al., 2009; Lamade et al., 2014), and cell turgor pressure. Mg is necessary for photosynthesis reactions as it is the central molecule of chlorophyll, and improves oil quality traits (Gerendás and Führs, 2013). K and Mg are also involved in enzyme mechanisms (Taiz and Zeiger, 2006). Substantial amounts of K are needed to ensure palm growth. Moreover, mineral (K and Mg) requirements are calculated on the basis of leaflet mineral concentrations to assess maximum growth and yield in oil palm industrial plantations (Dubos et al., 2019).

The main purpose of this study is to assess the growth and morphological characteristics of the selected oil palm progenies studied in order to reveal genotypic differences in plant growth under different fertilization regimes. In this study, we also evaluated the effect of fertilizers (KCl and kieserite) treatments on the progenies palms’ growth in Nigeria (West African) environment.

Table 1

Genetic characteristics, varieties, and genetic origins of the parents of the different oil palm progenies (PIC, 2011).

2 Materials and methods

2.1 Study site

The study was carried out in Nigeria, in one of the oil palm plantations belonging to Presco Plc company in Ologbo town near Benin-City (Supplementary Fig. S1), Edo State district (N6.03652° E 5.55609° at an elevation of 20 m a.s.l). Between 1996 and 2018, average annual rainfall in the study area in Nigeria was 2,066 mm (Bonneau et al., 2014). In the same period between 1996 and 2018, average annual temperatures ranged from 25.0 °C to 27.8 °C, and average annual radiation was 13.78 MJ m−2 d−1. Prior to the beginning of the experiment, the study site was a humid and largely degraded sub-tropical forest where cassava (Manihot esculenta) and plantain (Musa spp.) were cultivated after deforestation. The experimental land consisted of a vast sedimentary formation with a flat landscape containing ferralsols (FOA nomenclature) (Bonneau et al., 2017). Soils are deep, very sandy on the surface, with a gradual increase in clay content with depth and include no coarse elements. Soil fertility was low at the onset of the trial ( Tab. 2).

Table 2

Physico-chemical soil characteristics at the onset of the Nigerian trials.

2.2 Planting material

Four different oil palm (Elaeis guineensis Jacq.) progenies (progenies C1, C2 and C3 from Deli × La Mé origin, and progeny C4 from Deli × Yangambi origin; Tab. 1) were selected for this study among 116 high-yielding progenies that were previously studied in a varietal trial that aimed the comparison of their yield performances in Aek Loba Timur (Sumatera Utara province, Indonesia) (Ollivier et al., 2017). Between 4 to 7 years after planting (YAP) in Nigeria, average leaflet K concentrations were 0.857, 0.792, 0.725 and 0.981% of dry matter (DM) and average leaflet Mg concentrations were 0.260, 0.249, 0.301 and 0.269% of DM, for progenies C1, C2, C3 and C4, respectively (Dassou et al., 2018). All progenies used were Tenera crosses from two different genetic origins and were initially selected based on similar good fresh fruit bunch (FFB) and crude palm oil (CPO) production in Indonesia and subsequently on their contrasting leaflet K and Mg concentrations under equal fertilizer applications (PIC, 2011). The progenies are the result of collaborative breeding for oil palm yield improvement by the National Agricultural Research Institute of Benin (INRAB), the International Center of Agronomic Research for Development (CIRAD, France) and its subsidiary company PalmElit.

2.3 Seedling and palm fertilization management

Germinated seeds were treated in the pre-nursery and main nursery as recommended by CIRAD (2008). At the age of eight months in the nursery, only oil palm seedlings that met growth planting criteria were selected for the experiment: 0.6 to 1 m in height, 18 to 22 cm of collar girth, 6 to 8 functional fronds, and absence of disease or nutrient deficiency symptoms (CIRAD, 2008).

In the plantation, basal and uniform dressing fertilization was carried out in the first year after planting (YAP) so as to start the trial conditions as homogeneously as possible. In the second year, a basic application of urea (1,000 g palm−1) and triple superphosphate (500 g palm−1) was applied. Also, from the second year onwards, a gradient of K and Mg fertilizer amounts was applied during the first seven years in the main fertilizer plots. The fertilizer application schemes with three levels of fertilizer (K0–K1–K2 and Mg0–Mg1–Mg2, respectively) are presented in Table 3.

Table 3

Fertilizer application scheme in Nigeria (in g of fertilizer per palm).

2.4 Experimental design

The experimental design (Supplementary Fig. S2) consisted of a factorial split-plot trial with two factors: mineral nutrition (MN) × genetic material (GM), set up in Nigeria on about 33 ha with oil palms spaced 9 meters apart in a staggered, equilateral triangle design, resulting in a planting density of 143 plants ha−1 in 2011 (PIC, 2012). Measurements were taken for five years, from Y3 (2013) to Y7 (2017). All combinations of three levels of potassium chloride (KCl: 60% K2O) and three levels of kieserite (MgSO4: 27% MgO) were tested resulting in a total of nine fertilizer treatments considered as random effects in main plots, applied to the four oil palm progenies that were considered as subplots, resulting in a total of 36 subplots per replicate. The experiment consisted of six replicates, and therefore 216 subplots. Each subplot area was about 631 m2. In each subplot, data were collected from three rows of three studied (useful) palms, i.e. data were collected from a total of 1,944 useful palms in the trial. Within each, the useful palms were surrounded by border palms in all directions (45 border palms per fertilizer plot, or a total of 2,430 border palms for all 54 fertilized plots). About 350 additional border palms were planted along the sides of the road to protect the studied palms and their main border palms from attacks by rodents that may emerge from the adjacent forest.

3 Parameters measured

3.1 Growth factors

The averages of a number of oil palm growth parameters resulting from all the fertilizer treatments on the progenies were used to compare growth characteristics between the oil palm progenies in Nigeria. CIRAD–IGK protocols were used to measure growth:

  • oil palm height (Ph) was assessed from the fourth year on by measuring the length from petiole base (stump) of the leaf rank 33 to the soil surface. This measurement cannot be done before 3–4 YAP because until then, oil palm trees are stemless;

  • oil palm collar girth (CG) was determined by measuring the circumference of the stem at the soil surface;

  • oil palm frond length of rank 17 is the length of the petiole from the point closest to where the petiole is attached to the stem to the end of the rachis;

  • oil palm leaf area of rank 17 was assessed following Tailliez and Koffi (1992) by measuring the total length of the rachis and petiole of the frond rank 17, while the rachis length is divided into 10 sections, one normal (i.e. undamaged) leaflet is selected in the middle of each section and removed from the same side of the leaf in each section. The 10 leaflets are arranged on a pallet ranked according to their apparent size (Supplementary Fig. S3). Leaflet widths (in cm) are measured at 10 cm intervals along the leaflet. Each 10 cm section of the leaflet is then considered as a trapezium where the two widths measured at the top and bottom form the bases of the trapezium with a height of 10 cm. The remaining part of the leaflet (i.e., above the last section with a length of 10 cm) is considered to be an isosceles triangle. Leaflet area was then computed by adding all surface areas of each 10 cm trapezium-shaped leaflet section together with the area represented by the edge of the leaflet isosceles triangle.

The surface area of leaf 17 (l17a expressed in m2) was estimated as follow:(1)

(Eq. (1), Tailliez and Koffi, 1992), where:

  • n1 to n10 = number of leaflets per rachis section;

  • lft1 to lft10 = surface area of each selected leaflet from each section of the rachis.

Total leaf surface area of each progeny was obtained by multiplying the surface area of leaf 17 by the average number of new fronds emitted over the last four years.

The number of emitted fronds was counted following their rank appearance in the oil palm phyllotaxy described by IRHO (1960) and Fan et al., (2015);

  • oil palm projected canopy area on the ground was measured as a circle of which the palm trunk base was in the center;

  • oil palm stem volume (Vstem) was estimated as:


Oil palm height, collar girth and frond length are expressed in centimeters (cm), while leaf area and projected canopy area are expressed in cm2 and oil palm stem volume in cm3. Results of the trunk volumes are not presented in Figures 1 and 2.

3.2 Increase in growth factors

Yearly increases in oil palm stem height, number of emitted fronds and length of the rank 17 leaf were assessed from 4 to 7 years after planting (YAP). Additionally, yearly increases in oil palm collar girth and projected canopy area were assessed from 1 to 7 YAP, thus including the period from 1 to 3 YAP, during which oil palm stem diameters show the largest increases (Corley and Tinker, 2016). Annual increases in oil palm leaf area were recorded from 5 to 7 YAP. In each subplot, unproductive palms were withdrawn from the analysis.

3.3 Statistical analysis

A mixed model was used for the analysis of variance (ANOVA) of changes in growth factors. In this study, growth parameters were averaged across all fertilizer treatments. To account for the split-plot nature of the design, a mixed-effects model was used, with the sub-block effects (i.e., fertilizer × block interaction) as a random factor. The model was used to compare growth characteristics according to the progenies. Tukey’s multiple comparison test was applied to verify the significance of parameter means between progenies.

Statistical analyses were conducted in XLSTAT (Version 2018–7, and R version R-3.6.0 of Windows.

4 Results

4.1 Growth characteristics of oil palm progenies

Highly significant differences (P < 0.0001) were found between progenies for a number of vegetative growth parameters (Fig. 1). Differences in progenies’ genetic background (Tab. 1) show that only the number of emitted fronds (NEF) differed significantly in all four progenies in each studied year. In all progenies, the number of emitted fronds decreased each year until the plants reached 6 YAP, whereas all other parameters increased over the observation period. All growth parameters except palm tree height stabilized around 6–7 YAP. Height increased at an annual average rate of 41, 39, 42 and 43 cm in progenies C1, C2, C3 and C4, respectively, with no significant differences between the annual growth rates in progenies C3 and C4 (Fig. 1A).

The average number of emitted fronds per year was 27.5, 28.9, 28.6 and 31.5 for progenies C1, C2, C3 and C4, respectively. No significant difference in NEF was found between progenies C2 and C3 (Fig. 1B).

In all years, progeny C4 had the smallest average collar girth, whereas progenies C1 and C2 had the largest collar girth. Progeny C3 reached its maximum girth at 4 YAP (Fig. 1C). Considering the stem as a cylinder, progeny C3 compensated for its smaller diameter by its taller stature. Its trunk volume at 7 YAP (1.13 m3) was 3.9%, 17.6% and 6.8% higher than that of progenies C1 (1.09 m3), C2 (0.93 m3) and C4 (1.06 m3), respectively. Average annual girth increments in progenies C1, C2, C3 and C4, were respectively, 15.7, 18.2, 13.7 and 17.6 cm.

Progenies C1, C2 and C4 had similar frond lengths in all years, except in 5 YAP when progeny C4 had significantly shorter fronds. Progeny C3 had 20 to 30 cm higher frond length than progenies C1, C2 and C4. The average annual increase in frond length in C1, C2 and C4 was 37.7, 39.1, and 37.2 cm, respectively. The annual increase in frond length in progeny C3 (32 cm) was significantly lower than that in the other three progenies (Fig. 1D).

Progeny C3 had a larger projected canopy area than that of all the other progenies, in all measurement years. At 7 YAP, progenies C1, C2, C3 and C4 showed a mean annual increase in canopy projected area of 10.2; 11.4; 11.9 and 11.1 m2, respectively (Fig. 1E).

Progeny C3 had a significantly larger leaf area than the other progenies in all years (Fig. 1F). At 7 YAP, progeny C3 had 18% more leaf area than progenies C1 and C4, and 29% more than progeny C2 and its annual average total leaf area increase was 9%, 0.6% and 17% higher than that of progenies C4, C1 and C2, respectively.

Progeny C3 showed a better vegetative development (leaf length, leaf area and projected canopy area) than the other progenies in all measurement years.

thumbnail Fig. 1

Variation in the morphological parameters of oil palm progenies observed from 4 until 7 YAP. Different letters (a, b, c and d) indicate significant differences in the different parameters between oil palm progenies. YAP: year after planting. Capital letters (A, B, C, D, E and F) indicate the growth parameters measured.

4.2 KCl and kieserite effects on oil palm progeny growth

We found a significantly positive KCl effect in all progenies for the annual increase in collar girth, projected canopy area and area of leaf rank 17, whereas there was no effect for MgSO4 applications (P = 0.485). However, effects differed between progenies (Fig. 2A–F). We could not find significant differences between the four progenies for oil palm stem height increases between 4 and 7 YAP (Fig. 2A). Only in progeny C4 did increasing potassium applications (from K0 to K2) significantly (P = 0.0008) decrease the total number of fronds emitted annually between 4 and 7 YAP (Fig. 2B). In the latter progeny (C4), the annual number of emitted fronds decreased from 31.9 to 31.5 and 31.2 for K0 to K1 and K2 treatments, respectively (Fig. 2B).

In all progenies, a significant KCl effect was found for the average annual collar girth increment between 1 and 7 YAP. In progeny C1, the annual collar girth increment increased by 0.6 cm and 0.7 cm between K0–K1 and K1–K2 treatments, respectively, whereas in progeny C3, these increases were respectively 0.7 cm and 0.6 cm. Collar girth increments were only significant between K0–K1 for progenies C2 (1.4 cm) and C4 (1.3 cm) (Fig. 2C).

KCl significantly reduced the frond length increment from 43.7 cm (K0) to 38.0 cm (K1) and further (but not significantly) to 35.6 cm (K2) in progeny C2, and from 28.6 cm (K0) to 23.2 cm (K1) and further (but not significantly) to 20.9 cm (K2) in progeny C3 (Fig. 2D).

In all progenies, when compared to K0, K1 increased the projected canopy area, with 0.5, 0.7 and 0.8 m2 on average per year, for progenies C2, C3 and C4, respectively, whereas no significant differences were found in the projected canopy area for any of the progenies between K1 and K2. In progeny C1, only the projected canopy area increment of oil palms with treatment K2 was significantly different from that of the palms with treatment K0 (Fig. 2E). The area increment of leaf 17 only significantly increased in progeny C4 (from 1.62 m2 for K0 to 2.35 m2 for K2) (Fig. 2F).

Significant interaction (P < 0.001) between the effects of K and Mg applications was observed in all progenies for some studied years for several growth parameters (Supplementary Tab. S1). Moreover, K and Mg interactions was significant (P = 0.04) on average increase per year of projected canopy area, with treatments K2Mg0, K1Mg1 and K1Mg2 exhibiting higher and statistically similar average annual increases of projected canopy area, whereas K0Mg0 showed the lowest value and the other five K × Mg exhibited intermediate values.

K × progeny interaction was significant (P = 0.011) only for average leaf area increase with K2 × C3 exhibiting the highest average leaf area, whereas K2 × C2 and K0 × C4 showed the lowest average leaf area increase. For none of the growth parameters, there was a significant interaction between Mg and any of the progenies.

thumbnail Fig. 2

Stem height increase (A), number of emitted fronds per year (B), collar girth increase (C), annual length increase for leaf rank 17 (D), annual projected canopy increase (E) and annual leaf area increase (F) for oil palm progenies subjected to different KCl levels in Nigeria. The letters (a, b and c) explain the significant (P ≤ 0.05) differences between progenies observed at 7 years old, revealed by a Tukey test. YAP: year after planting.

5 Discussion

5.1 Growth characteristics of the four oil palm progenies

In a density trial in Obaretin (the second PRESCO oil palm plantation located in Benin-City (Edo state) in the same district as the current experiment), Bonneau et al., (2017) observed that average oil palm trunk length increased regularly and steadily with an annual growth rate of 35 cm, whereas the collar girth stabilized at around 265 cm at 9 YAP. The latter annual growth rate is lower than that of the progenies tested in the present study, in which annual growth rates ranged from 39 to 43 cm a year. This can be explained by the genetic differences between the progenies used in our study and those used by Bonneau et al. (2017) as well as the length of the observation period, which was 4 to 7 YAP in our study, compared 7 to 12 YAP in the study by Bonneau et al. (2017). According to Jacquemard and Baudouin (1987), oil palm trunks have a sigmoidal growth rate until 8–9 YAP, and a sigmoid decreasing growth rate from 10 YAP onwards. The differences between the growth rate in our study and that of Bonneau et al. (2017) might also be explained by local environmental conditions. In our trial, the soil was more fertile and rainfall/soil humidity was higher than in the study of Bonneau et al. (2017). Our experiment (Ologbo plantation) took place in a degraded forest zone whereas the Obaretin site (Bonneau et al., 2017) is located in an oil palm replantation area with lower soil organic matter content.

On average, growth parameters such as collar girth, tree height and the length of the rank 17 frond of the progenies tested in our study, were lower than those assessed by Bonneau et al. (2017) at the same age. The oil palm progenies tested in our study originate from breeding programs aiming at developing more compact planting material (i.e. with shorter internodes; Durand-Gasselin et al., 2000; Cochard et al., 2005; Konan et al., 2014). Above 13 m in height, oil palms are no longer economically viable because of increased cost of harvest (fruit bunches in tall palms are more difficult to harvest; Cochard et al., 2001; Konan et al., 2014). Estimating the age at which our progenies will reach a height of 13 m, taking into account their yearly increase in height, the expected life cycle of progenies C1, C2, C3 and C4, would be 32, 33, 31 and 30 years, respectively.

The progenies tested in this study have an average frond length of 6 m, which is the middle of the wide range of oil palm frond lengths (4 m to 8 m), as reported by Jourdan (1995).

In Benin, Nodichao et al. (2008) tested four oil palm progenies on trees aged 4 to 5 YAP and reported 26 to 30 fronds emitted per year. These numbers are in line with our results and confirm that the number of emitted fronds varies with oil palm progenies. Hartley (1988), Corley and Tinker (2016) reported that the frond emission rate decreases with age, which was also confirmed in our study. Corley and Tinker (2016) reported that the number of leaves produced each year by a plantation palm ranged between 30 and 40 at 2–4 YAP and gradually declined to 20–25 per year from 8 YAP onwards.

Rees and Tinker (1963) estimated leaf area values of 5.2, 6.7, 7.0, 9.9, 9.7 and 11.2 m2 for oil palms aged 7, 10, 14, 17, 20 and 22 YAP, respectively, near Benin-City in Nigeria, (WAIFOR: West African Institute for Oil palm Research, that subsequently became NIFOR: Nigerian Institute For Oil palm Research). At 7 YAP, palms of progeny C2 and C3 had the smallest and largest leaf area, respectively, which were respectively 1.08 and 1.4 times larger than that of the oil palms studied by Rees and Tinker (1963) at the same age. These differences are probably the result of progress made in oil palm breeding since the 1960s (Durand-Gasselin et al., 2000, Cochard et al., 2005).

In all progenies, leaf-related morphological parameters, i.e., frond length, projected canopy area and leaf area, reached maximum at 6 YAP, indicating that the physiological maturity of the leaves of the different progenies was reached at that age. The significant differences in growth variables observed among the progenies tested in our study are probably determined genetically (Nouy et al., 1999; Konan et al., 2014; Corley and Tinker, 2016), i.e. linked with the specific physiological traits of the different genetic origins of the oil palms (Jacquemard et al., 2002). This difference in growth morphology between progenies may also be related to differences in leaflet mineral concentrations which were found to be specific to each progeny (Dassou et al., 2022b).

5.2 Effect of K and Mg fertilizer applications on oil palm progeny growth

K fertilization has frequently been reported to have a positive effect on oil palm growth (Kusnu et al., 1996; Dubos et al., 1999; 2010; Bonneau et al., 2018). This was confirmed by our results for collar girth and projected canopy area in all progenies, as well as for the leaf area increase for progeny C4, which increased significantly with increasing KCl levels.

The negative effect of KCl on rank 17 frond length for progenies C2 and C3 might possibly be explained by the high yield (with increasing KCl levels) recorded between 5 to 8 YAP (Dassou et al., 2022a). Fruit bunches are mineral sinks that store K, to the detriment of K potentially accumulating in fronds (Dubos et al., 2010; Legros et al., 2006). The negative effect of K on frond length was more pronounced for progeny C3, which also had a higher bunch weight in comparison with progeny C2 (Dassou et al., 2022a). Moreover, only progenies C2 and C3 exhibited K- category among all progenies tested in this study, indicating that they have a low K status compared to progenies C1 and C4 which exhibited K+ status (Dassou et al., 2022b). However, the average projected canopy area of the palms of progenies C2 and C3 between 5 to 8 YAP increased with KCl levels when compared to the palms of the other progenies. This can be explained by their genetic background. Progenies C2 and C3 share the same female parent genotype, but have different male parent genes (Tab. 1).

The contrast between the positive effect of KCl on the average projected canopy area of the palms of progenies C2 and C3, and the negative effect on the increase in average rank 17 leaf length for the same progenies, might be explained by the fact that frond length was measured on the rank 17 fronds only, whereas the projected canopy area is determined by the most overarching oil palm leaves.

Our findings suggest that throughout the experimental period, the K2 treatment resulted in the highest and lowest average annual leaf area increase in progenies C3 and C2, respectively, in Nigerian ecological conditions. The fact that the same K rate (K2) induced contrasting growth development behaviors in two genetically different planting materials (progenies C2 and C3), underscores the need to assess mineral requirements (at least for K and Mg) of oil palm progenies in their specific ecological cultivation conditions.

Deli × Yangambi material (progeny C4) has a high, genetically determined frond emission potential compared to that of Deli × La Mé material (progenies C1, C2 and C3) (Corley and Tinker, 2016). The reduction in the number of emitted fronds with increasing KCl rates observed for the palms of progeny C4 was therefore probably linked to the yield increase observed for palms with treatments K1 and K2 compared to treatment K0, which may have depressed its vegetative growth (Dassou et al., 2022a).

The high frond emission in progeny C4 explained its high bunch number, as each frond is predestined to produce one inflorescence that can become male or female (Corley and Tinker, 2016). However, progeny C4 produced more male (69%) than female (31%) inflorescences (Dassou et al., 2022a). It is known that Deli × Yangambi material, such as C4 palms, produces relatively more male inflorescences in less favorable ecologies (Nouy et al., 1999), such as the one in our experiment (Nigeria) with lower rainfall conditions compared to Southeast Asia (Bonneau et al., 2014; Ollivier et al., 2017). This finding is important in solving low pollination problems (lack of pollen or very low male inflorescences production in the plantation) occurring in some oil palm plantations and suggests adding Deli × Yangambi material in, or around plantations composed of Deli × La Mé oil palm material which are known to be female material, having very high female inflorescences production (Dassou et al., 2022a).

The high development of aerial organs (length and area of leaf rank 17, projected canopy area) in C3 palms irrespective of fertilizer treatments, compared to those of the other progenies, might be explained by their genetic background. Many studies (Trehan, 2005; Marschner et al., 2007; Yanbo et al., 2008; Hassan et al., 2011) have demonstrated that efficient potassium use positively affects plant growth. However, further studies are needed to verify whether the palms of progeny C3 indeed have a relatively higher potassium use efficiency than the other progenies.

Growth parameters were unaffected by our Mg treatments, which was also found by Kusnu et al. (1996) and Bonneau et al. (2018). This lack of MgSO4 effect on growth parameters might be explained by the fertility of the soil in our trial, which had high levels (as generally found in ferralsols in tropical zones) of exchangeable Mg (Tab. 2). As a result, Mg was abundantly available to our oil palms and supplying more Mg had no effect on growth parameters (Kusnu et al., 1996).

6 Conclusion

All progenies were shown to have different morphological growth traits with progeny C3 producing the most biomass in Nigeria’s environment. Our results suggest that differences in progenies’ growth are the result of their genetic background. Potassium is the main mineral involved in oil palm morphological growth and development in Nigeria’s environment, compare to magnesium. However, with 3 kg KCl palm−1 (K2), progeny C3 developed the highest annual leaf area growth whereas progeny C2 exhibited the lowest value, suggesting the need of assessing the mineral requirements (at least for K and Mg) of different planting materials in their specific ecological cultivation conditions found in Nigeria according to their specific needs.

Conflict of interests

Olivier DASSOU, Hervé Aholoukpè and Apollinaire Mensah are employed by INRAB. Stephen Peprah is employed by Presco. Jean Ollivier, Xavier Bonneau and Albert Flori are employed by CIRAD of which PalmElit is subsidiary company and of which Tristan Durand-Gasselin is the CEO. All these companies have a collaborative partnership.

The authors declare they have no known competing financial interests or personal relationships that could have influenced the work reported in this paper.

Supplementary material

Fig. S1. Map of Africa showing the location of Nigeria in Africa (left) and Benin-City and Ologbo oil palm estate in Nigeria (right).

Fig. S2. Experimental layout.

Fig. S3. Graduated pallet with leaflets ranked according to their apparent leaflet area. Source: Tailliez and Koffi (1992).

Table S1. K × Mg interactions on oil palm growth parameters.

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The authors sincerely acknowledge the Islamic Development Bank (IsDB) for funding the first author’s PhD with which the present research was conducted. We further thank INRAB, CIRAD, PRESCO, PT SOCFINDO and UGent for their technical and financial support.

We express our sincere gratitude to the technical staff of the PRESCO R&D department for help with the collection of field data. Special thanks to Cecile Bessou and Alexis Thoumazeau (CIRAD) for their advice and for reviewing this article.


  • Baudouin L, Baril C, Clément Demange A, Leroy T, Didier P. 1997. Recurrent selection of tropical tree crops. Euphytica 96: 101–114. [CrossRef] [Google Scholar]
  • Bonneau X, Impens R, Dassou O, Ogiamien F, VanDamme P. 2018. Optimal fertilization for oil palm (Elaeis guineensis Jacq.) plantations: conclusions from a long-term fertiliser trial in Nigeria. In: Tielkes E., ed. Tropentag, Ghent “Global food security and food safety: the role of universities. Book of abstracts, 594 p. Online book of abstracts, available from: [Google Scholar]
  • Bonneau X, Impens R, Buabeng M. 2017. Optimum oil palm planting density in West Africa. OCL . 10 p. [Google Scholar]
  • Bonneau X, Vandessel P, Buabeng M, Erhahuyi C. 2014. Initial results of an oil palm planting density experiment in west Africa. OCL . [Google Scholar]
  • CIRAD. 2008. Semences germées de palmier à huile CIRAD : recommandation pour la conduite de la pré-pépinière et de la pépinière. Édition scientifique : Jean-Charles Jacquemard et Dominique Boutin, 28 p. [Google Scholar]
  • Cochard B, Amblard P, Durand-Gasselin T. 2005. Oil palm genetic improvement and sustainable development. OCL 12(2): 141–145. [CrossRef] [EDP Sciences] [Google Scholar]
  • Cochard B, Adon B, Kouamé KR, Durand-Gasselin T, Amblard P. 2001. Intérêts des semences commerciales améliorées de palmier à huile (Elæis guineensis Jacq.). Oléagineux, Corps Gras, Lipides 8(6): 654–658. [CrossRef] [EDP Sciences] [Google Scholar]
  • Corley RHV, Tinker PB. 2016. The oil palm. Oxford: Blackwell Science Ltd., 687 p. [Google Scholar]
  • Dassou O, Nodichao L, Ollivier J, et al. 2018. Oil palm (Elaeis guineensis Jacq.) leaf K and Mg contents differ with progenies: implications and research needs. In: Tielkes E, ed. Tropentag, Ghent “Global food security and food safety: the role of universities. Book of abstracts. 594 p. Available from [Google Scholar]
  • Dassou SO, Adjanohoun A, Vanhove W, et al. 2022a. Oil palm (Elaeis guineensis Jacq.) genetic differences in mineral nutrition: specific leaflet mineral concentrations in high-yielding oil palm progenies and their implications for managing K and Mg nutrition. Plant and Soil . 14 p. [PubMed] [Google Scholar]
  • Dassou SO, Ollivier J, Vanhove W, et al. 2022b. Oil palm (Elaeis guineensis Jacq.) genetic differences in mineral nutrition: environmental effects on leaflet mineral concentrations of four oil palm progenies. OCL . 11 p. [Google Scholar]
  • Dubos B, Baron V, Bonneau X, et al. 2019. Precision agriculture in oil palm plantations: diagnostic tools for sustainable N and K nutrient supply. OCL 26: 5. [CrossRef] [EDP Sciences] [Google Scholar]
  • Dubos B, Hernán W, Jesùs A, Lòpez E, Ollivier J. 2010. Potassium uptake and storage in oil palm organs: the role of chlorine and the influence of soil characteristics in the Magdalena valley, Colombia. Nutr Cycl Agroecosyst . [Google Scholar]
  • Dubos B, Caliman JP, Corrado F, Quencez P, Siswo S, Tailliez B. 1999. Rôle de la nutrition en magnésium chez le palmier à huile. Plantation − Recherche − Développement : 313–325. [Google Scholar]
  • Durand-Gasselin T, de Franqueville H, Breton F, et al. 2011. Breeding for sustainable palm oil. Int Semin Breed Sustain Oil Palm : 178–193. [Google Scholar]
  • Durand-Gasselin T, Cochard B, Amblard P, Nouy B. 2009. Exploitation de l’hétérosis dans l’amélioration génétique du palmier à huile (Elæis guineensis ). Le Sélectionneur français 60: 91–100. [Google Scholar]
  • Durand-Gasselin T, Hayun S, Jacquemard JC, et al. 2006. Palm oil yield potential of oil palm (Elaeis guineensis) seeds developed in a network by Cirad and its partners. In: International Workshop int the Yield Potential in the Oil Palm, Phuket, Thailand 27–28 November 2006. ISOPB. s.l.: s.n., 15 p. [Google Scholar]
  • Durand-Gasselin T, Kouame R, Cochard B, Adon B, Amblard P. 2000. Diffusion variétale du palmier à huile (Elaeis guineensis Jacq.). Oléagineux, Corps Gras, Lipides 7(2): 207–214. [CrossRef] [EDP Sciences] [Google Scholar]
  • Fan Y, Roupsard O, Bernoux M, et al. 2015. A sub-canopy structure for simulating oil palm in the Community Land Model (CLM-Palm): phenology, allocation and yield. Geosci Model Dev 8: 3785–3800. Available from [CrossRef] [Google Scholar]
  • Gerendás J, Führs H. 2013. The significance of magnesium for crop quality. Plant Soil 368: 101–128. [CrossRef] [Google Scholar]
  • Goh KJ, Teo CB, Chew PS, Chiu SB. 1999. Fertiliser management in oil pal: agronomic principples and field practices. Paper presented at “Fertilizer Management For Oil Palm Plantations”, 20–21 September 1999, Sandakan, Sabah, Malaysia. Organised by ISP, Sabah North-East Branch. [Google Scholar]
  • Hartley CWS. 1988. The oil palm. Singapore: Longman Singapore Publishers (Pte) Ltd., 761 p. [Google Scholar]
  • IRHO. 1960. Protocole d’une méthode globale d’observations végétatives sur le palmier à huile. IRHO, 25 p. [Google Scholar]
  • Hassan Z, Arshad M, Khalid A. 2011. Evaluating potassium use efficient cotton genotypes using different ranking methods. Journal of Plant Nutrition : 27 p. [Google Scholar]
  • Jacquemard JC, Tailliez B, Dadang K, Ouvrier M Asmady H. 2002. Oil palm (Elaeis guineensis Jacq.) nutrition: Planting material effect. In: International Oil Palm Conference and Exhibition, 08–12 July 2002, Bali, Indonesia. [Google Scholar]
  • Jacquemard JC, Baudouin L. 1987. Contribution à l’étude de la croissance du palmier à huile. Présentation d’un modèle descriptif. Oléagineux 42(10): 343–351 (3 ill; 14 réf; 6 Tabl.). [Google Scholar]
  • Junaidah J, Rafil FY, Chin CW, Saleh G. 2011. Performance of Tenera oil palm population derived from crosses between Deli Dura and Pissifera from different sources on inland soil. Journal of Oil Palm Research 23: 1210–1221. [Google Scholar]
  • Jourdan C. 1995. Modélisation de l’architecture et du développement du système racinaire du Palmier à huile (Elaeis guineensis Jacq.). Thèse de doctorat. Montpellier II: Université des sciences et techniques du Languedoc, 243 p. [Google Scholar]
  • Konan JN, Allou D, Diabate S, Konan EP, Koutou A. 2014. Évaluation de l’introgression du caractère croissance lente de quelques géniteurs Akpadanou (origine Bénin) chez quelques géniteurs améliorés de palmier à huile (E. guineensis Jacq.) de l’origine La Mé (Côte d’Ivoire). Int J Biol Chem Sci 8(5): 2015–2022. Available from [CrossRef] [Google Scholar]
  • Kusnu M, Siahaan MM, Poeloengan Z. 1996. Effects of N, P, K and Mg fertilizer on the growth and yield of oil palm on Typic Paleudult. In: Sustainability of oil palm plantations. Agronomic and Environmental perspectives, Kuala Lumpur, 27–28 September. ISOPA, PORIM, 14 p. [Google Scholar]
  • Lamade E, Ollivier J, Rozier-Abouab TH, Gérardeaux E. 2014. Occurrence of potassium location in oil palm tissues with reserve sugars: consequences for oil palm K status determination. In: IOPC conference, 17–19 June, Bali Convention Center, oral communication. [Google Scholar]
  • Legros S, Mialet-Serra I, Clement-Vidal A, et al. 2009. Role of transitory carbon reserves during adjustment to climate variability and source-sink imbalances in oil palm (Elaeis guineensis). Tree Physiology 29: 1199–1211. [CrossRef] [PubMed] [Google Scholar]
  • Legros S, Mialet-Serra I, Caliman JP, et al. 2006. Carbohydrates reserves in 9 years old oil palm: nature, distribution and seasonal changes. In: IOPC − Optimum use of resources: Challenges and opportunities for sustainable oil palm developpement, Bali. [Google Scholar]
  • Marschner P, Solaiman Z, Rengel Z. 2007. Brassica genotypes differ in growth, phosphorus uptake and rhizosphere properties under P − limiting conditions. Soil Biol Biochem 39: 87–98. [CrossRef] [Google Scholar]
  • Nodichao L, Aké S, Jourdan C. 2008. Développement du système racinaire chez le palmier à huile selon l’origine génétique et le régime hydro-potassique du sol. Agronomie africaine 20(3): 277–289. [Google Scholar]
  • Nouy B, Baudouin L, Djégui N, Omoré A. 1999. Oil palm under limiting water supply conditions. Plantations, Recherche, Développement 6: 31–45. [Google Scholar]
  • Ollivier J, Flori A, Cochard B, et al. 2017. Genetic variation in nutrient uptake and nutrient use efficiency of oil palm. Journal of Plant Nutrition 40(4): 558–573. [CrossRef] [Google Scholar]
  • PIC. 2012. Rapport du Programme d’Intérêt Commun (PIC) entre INRAB–CIRAD et PalmElit : bilan exercice 2011 – perspective 2012. [Google Scholar]
  • PIC. 2011. Rapport du Programme d’Intérêt Commun (PIC) entre INRAB–CIRAD et PalmElit: Bilan exercice 2010 – perspective 2011. [Google Scholar]
  • Prabowo E, Foster LH, Nelson S, Sitepu B, Nelson P. 2012. Practical use of oil palm nutrient physiological efficiency with regard to nutrient recovery and agronomic efficiencies at different Sumatran sites, 19 p. [Google Scholar]
  • Rees AR, Tinker PBH. 1963. Dry-matter production and nutrient content of plantation oil palms in Nigeria. I − Growth and dry matter production. Plant and Soil 19(1): 19–32. [CrossRef] [Google Scholar]
  • Rival A, Levang P. 2010. La palme des controverses : palmier à huile et enjeux de développement. Versailles: Édition Quae, 16 p. [Google Scholar]
  • R 3.6.0 for Windows, 32/64 bit. [Google Scholar]
  • Skurtis T, Aïnache G, Simon D. 2010. Le financement du secteur de l’huile de palme : pourquoi les institutions financières de développement doivent continuer à investor en Afrique. OCL 17 (6): 400–403. [CrossRef] [EDP Sciences] [Google Scholar]
  • Taiz L, Zeiger E. 2006. Plant physiology. 4th ed. Massachusetts: Sinauer Associates Inc. Publishers. [Google Scholar]
  • Tailliez B, Koffi BC. 1992. A method for measuring oil palm leaf area. Oléagineux 47(8–9): 537–545. [Google Scholar]
  • Trehan SP. 2005. Nutrient Management by exploiting genetic diversity of potato − a review. Potato J 32: 1–15. [Google Scholar]
  • USDA. 2020. Oilseeds World Markets and Trade: Global Consumption Recovers in 2020/21 After 2019/20 Drop. United States Department of Agriculture Foreign Agricultural Service, 50 p. [Google Scholar]
  • Verheye W. 2010. Growth and production of oil palm. In: Verheye W, ed. Land Use, Land Cover and Soil Sciences. Encyclopedia of Life Support Systems (EOLSS). Oxford, UK: UNESCO-EOLSS Publishers. Available from [Google Scholar]
  • XLSTAT. Version 2018-7. [Google Scholar]
  • Yanbo J, Xiaoe Y, Ejazul I, Ying F. 2008. Effects of potassium deficiency on chloroplast ultrastructure and chlorophyll fluorescence in inefficient and efficient genotypes of rice. Journal of Plant Nutrition 31(12): 2105–2118. [CrossRef] [Google Scholar]

Cite this article as: Dassou OS, Bonneau X, Aholoukpè H, Vanhove W, Ollivier J, Peprah S, Flori A, Durand-Gasselin T, Mensah AG, Sinsin BA, Van Damme P. 2022. Oil palm (Elaeis guineensis Jacq.) genetic differences in mineral nutrition: potassium and magnesium effects on morphological characteristics of four oil palm progenies in Nigeria (West Africa). OCL 29: 31.

All Tables

Table 1

Genetic characteristics, varieties, and genetic origins of the parents of the different oil palm progenies (PIC, 2011).

Table 2

Physico-chemical soil characteristics at the onset of the Nigerian trials.

Table 3

Fertilizer application scheme in Nigeria (in g of fertilizer per palm).

All Figures

thumbnail Fig. 1

Variation in the morphological parameters of oil palm progenies observed from 4 until 7 YAP. Different letters (a, b, c and d) indicate significant differences in the different parameters between oil palm progenies. YAP: year after planting. Capital letters (A, B, C, D, E and F) indicate the growth parameters measured.

In the text
thumbnail Fig. 2

Stem height increase (A), number of emitted fronds per year (B), collar girth increase (C), annual length increase for leaf rank 17 (D), annual projected canopy increase (E) and annual leaf area increase (F) for oil palm progenies subjected to different KCl levels in Nigeria. The letters (a, b and c) explain the significant (P ≤ 0.05) differences between progenies observed at 7 years old, revealed by a Tukey test. YAP: year after planting.

In the text

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