African Journal of
Plant Science

  • Abbreviation: Afr. J. Plant Sci.
  • Language: English
  • ISSN: 1996-0824
  • DOI: 10.5897/AJPS
  • Start Year: 2007
  • Published Articles: 808

Full Length Research Paper

Potential and measures for sustaining Prunus africana (Hook.F.) Kalkman (Rosaceae) in Tchabal Mbabo forest (Mf), Adamaoua Cameroon

Ndedy Bile Armand Wilfried
  • Ndedy Bile Armand Wilfried
  • Department of Plant Biology, Faculty of Science, B.P. 24157 Douala, Cameroon.
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Mpouam Alain Rayane
  • Mpouam Alain Rayane
  • Department of Plant Biology, Faculty of Science, B.P. 24157 Douala, Cameroon.
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Betti Jean Lagarde
  • Betti Jean Lagarde
  • Department of Plant Biology, Faculty of Science, B.P. 24157 Douala, Cameroon.
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Fono Louis Aimé
  • Fono Louis Aimé
  • Department of Mathematics and Computer Science, Faculty of Science, B.P. 24157 Douala, Cameroon.
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Kourogue Liliane Rosine
  • Kourogue Liliane Rosine
  • Department of Plant Biology, Faculty of Science, B.P. 24157 Douala, Cameroon.
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Fouadjio Benoit Jean
  • Fouadjio Benoit Jean
  • Department of Plant Biology, Faculty of Science, B.P. 24157 Douala, Cameroon.
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Yimga Michele Flore
  • Yimga Michele Flore
  • Department of Plant Biology, Faculty of Science, B.P. 24157 Douala, Cameroon.
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Wete Eric
  • Wete Eric
  • Department of Plant Biology, Faculty of Science, B.P. 24157 Douala, Cameroon.
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Njimbam Oumar Farick
  • Njimbam Oumar Farick
  • Department of Plant Biology, Faculty of Science, B.P. 24157 Douala, Cameroon.
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Nana Afiong Natacha
  • Nana Afiong Natacha
  • Department of Plant Biology, Faculty of Science, B.P. 24157 Douala, Cameroon.
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Fils Billong Pascal
  • Fils Billong Pascal
  • Department of Plant Biology, Faculty of Science, B.P. 24157 Douala, Cameroon.
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Ela Marius
  • Ela Marius
  • Department of Plant Biology, Faculty of Science, B.P. 24157 Douala, Cameroon.
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Tassiamba Steve
  • Tassiamba Steve
  • Departement of Forestry, Faculty of Agronomy and Agricultural Sciences, B.P. 222 Dschang, Cameroun.
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Tientcheu Stephanie
  • Tientcheu Stephanie
  • Department of Plant Biology, Faculty of Science, B.P. 24157 Douala, Cameroon.
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Bem Eleanor
  • Bem Eleanor
  • Department of Plant Biology, Faculty of Science, B.P. 24157 Douala, Cameroon.
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Guedem Christine
  • Guedem Christine
  • Department of Plant Biology, Faculty of Science, B.P. 24157 Douala, Cameroon.
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  •  Received: 23 March 2022
  •  Accepted: 27 June 2022
  •  Published: 31 August 2022


Prunus africana (Hook. F.) Kalkman is a medicinal plant for which the bark is used to treat benign prostate hypertrophy. P. africana is listed in Appendix 2 of the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES). Its exploitation has been regulated in Cameroon through the settlement of some management standards. This paper aims to assess the potential of P. africana in the Tchabal Mbabo forest (MF), vast of 25,671 ha in view to formulate guidelines for sustainable harvesting. Data collection took place from October 1st to 28th 2021. This consisted of conducting forest management inventories at a sampling rate of 0.72%. Three hundred and fifty-eight (358) stems of P. africana were counted on a surface area of 57.5 ha, which gives a density of 6.23 stems/ha. The average values of diameter, height and bark thickness of the stems (unharvested and harvested sides) are respectively 48.17 ± 19.8 cm; 7 ± 4.26 m; 14.1 ± 4.72 mm and 10.39 ± 4.22 mm. The average annual bark increment is 1.3 mm/year for a bark regeneration rate of 60%. A half rotation of 7 years was obtained for a dry bark quota of 164.6 tons/year. It would be wise to take into account the dynamic elements to review the calculation of the quota for the second rotation.


Key words: Prunus africana, standards, parameters, sustainable management, Tchabal Mbabo.


Cameroonian forests with 22.5 million hectares are among the vast and rich forest  massifs in the Congo basin (Wete, 2022). During the last decade of the twentieth century, the  role of forest was again redefined by include additional parameters such as carbon sequestration, biodiversity, regeneration status, and Non-Timber Forest Product (NTFP) (Tewari, 2016). The NTFP from these forests bring together food plants, medicinal plants and service products (Betti et al., 2016). The use of plants for therapeutic purposes has been known since the dawn of time (Lehmann, 2013). Today, the effectiveness of herbal medicine is proven and its undeniable benefits (Bene et al., 2016). Among the health problems listed, the prostate cancer is an important public health problem (Shenouda et al., 2007). According to Diarra (2006), apart from cancer proper, other prostate conditions are generally associated with it, amongst them we have the benign prostate hypertrophy (HBP). It is a non-cancerous prostate enlargement (Nyamai et al., 2016) which causes discomfort in elderly men, present in more than 50% of men over 60 years (Bodeker et al., 2014). Medicine by plants becomes daily (Bene et al., 2016) because,The conventional methods lead to severe side effects including erectile dysfunction and gynecomastia. So, people prefer to opt for phytotherapy for the management of the condition to avoid these adverse effects (Nyamai et al., 2015).


The use of Prunus africana in traditional African medicine (ATM) to treat prostate cancer and related conditions is not a new phenomenon in various communities in Africa (Ochwang'i, et al., 2014; Komakech et al., 2017). Mutuma et al. (2020) confirms that the dichloromethane stem bark extract of the P. africana presented anti-inflammatory activity, hence a possible candidate for extraction of active anti-inflammatory compounds. Its importance resides in the curative properties of its bark extracts used for the manufacture of more than 19 drugs, sold on the European and American markets for the treatment of benign prostatic hypertrophy (Cunningham et al., 2002). These extracts are mainly made up of of pentacyclic triterpenoids, ferulic esters of long-chain fatty alcohols, and phytosterols contained in bark and find in certain drugs, for e.g., Tadenan, Bidrolar and Pygenil (Nyamai et al., 2016; Komakech et al., 2017). The worldwide demand for these barks is estimated at 4000 tons (Simons et al., 1998). This high demand has therefore led to irrational harvesting of the plant species in the various production areas. Thus, trees have been felled abundantly and frequently before the maturation stage or debarked completely at the trunk level (Randriambololona, 1994; Rasoanandrasana, 2010). As a result of this intensive exploitation and poor harvesting methods, P. africana has become very scarce, the rootstock has disappeared and its natural regeneration has been reduced (Dawson and Rabevohitra, 1996; Sven and Rakotonirina, 1995; Rasoanandrasana, 2010; Momo et al., 2016). All this led to the listing of the species in Appendix II of the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES) in 1995 (Tonye et  al.,  2000).  In  Cameroon  the  majority  of  P. africana populations are found in the North West, South West and Adamaoua regions where they have been widely exploited for their bark since 1980 (Momo et al., 2016).


A key requirement of CITES for any species listed in appendix II is the establishment of a non-detriment findings made by the Scientific Authority of the range State prior to export, certifying that export is not detrimental to the survival of the species. This requires information on the location, stocking, growth and condition of the species and on its ecology, regeneration and subsequent protection. Such information is often lacking, incomplete or imprecise making a proper evaluation of the sustainable levels of utilization and conditions attached to be difficult. The Scientific Authorities also face obstacles due to inadequately trained and resourced staff. Following irregularities observed in some range of countries, a conference was organized by CITES in September 2008 in Lima, Peru with a view to deciding on the management methods of P. africana in exporting countries. During this conference, some countries, such as Cameroon, were asked to voluntarily consider a zero-export quota before December 31st, 2008, in order to conduct forest inventories and develop the management plan for P. africana. Failure to comply with these recommendations could lead to an embargo on trade in this species from these countries (Ingram et al., 2009). In the meantime, this deficiency observed in the management of P. africana in Cameroon led the European Union (EU) to suspend exports from Cameroon in 2008 (Akoa et al., 2010). The exploitation of P. africana resumed in Cameroon only in 2010 after the first results of the management inventories which led to the development of a non-detriment finding document (NDF) for this species in the North-West Region, Cameroon (Akoa et al., 2010).


This work, carried out within the framework of the joint program of the International Tropical Timber Organization (ITTO) and the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES), known as "The ITTO-CITES program”, was extended in the southwest (Akoa et al. 2011a) and then in Adamaoua (Akoa et al., 2011b) regions and allowed Cameroon to be granted an annual quota of 630 tons of dry bark of P. africana in 2011 and distributed as follows: Adamaoua (350 tons), North-West (150), and South-West (170). All these interventions have enabled Cameroon to take ownership of the management mechanisms of CITES species. However, the reports of certain NGOs and in particular the Deutsche Gesellschaft fur Internationale Zusammenarbeit GmbH (GIZ) always mentioned the unsustainable management of the Pygeum, so, CITES called on Cameroon on this subject and in particular on the reduction of export quotas ( Until September 2017, Cameroon had not yet provided clear answers to all CITES recommendations, especially on the real potential of each production unit of P. africana. The state of the art on the management/harvesting of P. africana in Cameroon revealed that, for the Adamawa Region, forest inventories carried out by trade companies themselves were not conducted in fair manner, using approved standards settled by the Cameroon forest management guidelines. Furthermore, the management parameters used to estimate the annual quota is based on studies conducted in the North west and South west regions of Cameroon (Wete, 2022). The commercialization of medicinal plants needs to account for the limits of the resource to ensure the sustainable, i.e., the long-term and continued, harvesting of the species (Bodeker et al., 2014).The present work attempts to assess the potential of P. africana with the view to ensure sustainable exploitation of the bark of this species in the Tchabal Mbabo forest (MF). The specific objectives are: (1) to analyze the sampling effort in mountain forests (2) to appreciate the structural parameters (density, diametric structure, basal area, carbon stock) (3) to characterize the response of Prunus trees to the harvesting (sanitary statement, bark regeneration) (4) and to propose sustainable management measures for bark harvesting (rotation, harvesting zones, harvesting techniques). 


Study site


Tchabal Mbabo is geographically located in the Adamaoua Region, on either side of the Departments of Mayo Banyo and Faro and Déo, in three subdivisions including Banyo in the Mayo Banyo Division, Galim Tignère and Kontcha in the Faro and Déo Division (Hiol Hiol, 2021). It culminates at an altitude of 2240 meters (MINFOF, 2018). The work was conducted in 4 localities namely: Foungoi with coordinates (07°14’04.51”N, 12°02’56.96”E), Yangare (07°13’42.47”N, 12°07’57.40”E), Botendji (07°14’49.41”N, 12°10’07.29”E) and Horé garba (07°19’22.98”N, 12°14’02.45”E). The human population of the area comprises diverse ethnic groups including Mbororos, Foulbes, Nyem Nyems and Hauossas. These groups are divided into traditional chiefdoms or Lamida and different native languages (Unsongo, 2019). The main vegetation of Tchabal Mbabo is made up of forest galleries, grassy savannas, dry altitude forests, and wooded savannas. Forest galleries are known to be predilection sites for P. africana (Wete, 2022). The North and south of the Adamaoua plateau is made up of metamorphic rocks and granitoids of African panic age. It is crossed in the north and east by basalt flows and cones, domes and trachyte-colored domes and phonolitis of mio-plicen ages (Fagny et al., 2017). Tchabal Mbabo hosts 294 bird species, 22 species restricted to the afro montane ecosystem, 10 of which are endemic to the mountain chain. The area is also known to harbour some Critically Endangered and Endangered reptiles and amphibians (Usongo, 2019). The hottest months are April and May with average daily temperatures of up to 30°C. Annual temperatures on the plateau average 18°C with daily amplitude of 13-15°C (Herrmann et al., 2007). Figure 1 present the ombrothermic diagram of the zone.



Description of the species


P. africana grows well in the sub-mountain and mountain forests at an altitude of 800-3000 m. In Cameroon, the plant  is  largely found in five regions including Adamaoua, North West, Littoral, South west, and West (Betti and Ambara, 2013). The description made by Vivien and Faure (2011) is as follows: Its base is a simple wheelbase or thick 8 -10 cm thick, deviating at 1 m of the tree at 1 m in height. It was straight with a crown with tortuous branches eased obliquely with young reddish twigs. It’s very dark brown bark (1.5 cm) formed large or less square platelets in the aged trees; It tender, fibrous, pink turning brown, with characteristic odor of bitter almond little differentiated, pinkish white (3 cm). Its wood is brown pink in Iight with leaves persistent, alternate, simple (6-15 x 3-6 cm), with a tender and shiny then tough and matt blade, on a crenellated edge with a small black gland at each point, sometimes 1 or 2 glands at the base of the blade, At 6-12 pairs of side veins. Its fruit is a drupe with 2 red lobes, with a small point at the top.




The method used is a combination of surveys and forest inventories. The surveys were conducted using the participatory method to get an idea of the actual production sites of P. africana in the Tchabal Mbabo forest. Discussions were conducted with administrative officials, including forestry services, community representatives, traditional chiefs or Djaouro, village populations (elderly and non-elderly), and field-based staff of companies that harvest P. africana in Cameroon. P. africana inventories were carried out in areas previously identified as P. africana production sites from October 1st to 28th 2021. The method used is, the classical forest inventory method standardised (arêté n° 222) for management inventories (MINEF, 2001).


Sampling design


The surveys carried out made it possible to map and delimit the potential sites of predilection of P. africana in altitudes ranging from 1,400 to 2,100 m. Maps were made in three stages ,including: (1) document review and exploration of photos and images (2) identification of areas to be surveyed, and (3) refinement of the data. The BING and (Open Street Map) OSM aerial funds were used for this purpose. The elevation factor proved to be of primary importance in the spatial distribution of P. africana in the inventory area, so we made a Digital Terrain Model (DTM) on which the information layers were draped. The DTM was made by downloading a LANDSAT 8 image of March 2021 of the inventory area and then processed on QGIS 3.0. For this inventory, “layons” were oriented in the direction perpendicular to the general direction of slope, according to the national standards (MINFOF, 2019), the sampling is systematic and stratified to 1 degree when the statistical unit is the plot. The samples or plots of 0.5 ha (250 m long × 20 m large) are distributed systematically throughout the entire population and not by stratum (forest type). The stratification is done definitively after the sampling. The systematic disposal of plots allows the assumption that the intensity of sampling for each stratum is proportional to its area in the forest. Results of the inventory and their accuracy are calculated for each stratum. In practice, sampling is carried out along straight and continuous axes called “layons” or transects. These “layons” are oriented along a predetermined magnetic direction but are systematically arranged in such a way that they are mostly parallel, equidistant and perpendicular to the general direction of both drainage and slopes. In Cameroon, the sampling intensity for management inventories, the surveys conducted have estimated the useful area of P. africana in the Tchabal Mbabo to be 28,456 ha. For this work, a total of four villages were selected because of (1) their accessibility and (2) of the consent of the village leaders. The total area selected is 8,000 ha distributed as follows in the four villages: Foungoi (1,846.48 ha), Yangaré  (3,018.97),  Botendji  (1,011.14)  and  Horé Garba (2,123.41). A provisional sampling rate of 2% was designed. Figure 2 illustrates the sampling design.



Implementation of the sampling design


The implementation of the sampling design (or the inventory) consists of two steps: “layons” or line opening/transect cutting and counting. Line opening/transect cutting: This step consists of opening or cutting according to a defined magnetic direction, corridors or alleys of 1.5 m wide. These corridors are clearly cleaned by cutting shrubs, vines and branches that obstruct the passage. They are then identified by marks. “Layons” constitute the reference system which will be used by the subsequent counting team. It is during the “layons” opening that details on topography, habitat types, rivers and the corrected horizontal distance of the “layon” (after reading the slopes) are given. It is also during this stage that the sample plots are identified and numbered. The data collected are recorded on specific sheet. Counting: The counting step includes all operations relating to dendrological and dendrometric records. During the counting, several operations are made including: Identification of stems of P. africana, the measurement of stems with diameter at breast height (dbh = 1.30 m)>= 5 cm, appreciation of the health state of the tree in three classes (dead trees, damaged trees, and living trees). The appreciation of the healthy status of the tree is mainly based on the health of the leaves and number of dried branches. Lines and plots are identified and numbered with their geographical coordinates and altitudes. For each P. africana stem encountered, the height, diameter at breast height, bark thickness was measured. The thickness was measured for each exploited stem on the face of the bark not yet exploited as well as on the face of the bark already exploited, that is, the bark in regeneration. For this purpose, a square or rectangular bark core was taken and the thicknesses of the four sides were measured. The average thickness of the four sides was taken as the bark thickness of this tree and for the indicated side. The harvesting techniques used were described and the year of harvesting was noted. 


Data analysis


The processing of the collected data allowed highlighting density, basal area, diametric structure, bark reconstitution rate, carbon stock, and half-rotation. The formulas used are the following:


Density is expressed as:


D = Ni / Ss


with Ni: number of stems counted; Ss: area surveyed.


Basal area is G = ∑ (π D²/4)


with D: stem diameter and π =3.14.


The average annual increment of reconstituted bark is:


AAMEr = EMCe / t


where EMCe: average thickness on logged side; t: time between logging and collection date.


The rate of reconstitution in thickness of the exploited bark is:


TREee = EMCe / EMCne


with EMCne: average of the thicknesses on the non-exploited side.


The evolution of the average annual increase in thickness of the unharvested  side  over  time  was  assessed  from  the  ratio of the thickness of the unharvested side to the diameter. RCneD = EMCne / MDhp with MDhp: mean diameter at breast height. The Ho assumption here is that the average annual increase in thickness of the unharvested bark increases with diameter over the same period of time. The formula for calculating quotas is: Qa = De × R × Su / T where Qa: Annual harvesting quota; De: Density of harvestable stems; R: Productivity or yield in kilograms of dry stem bark from a stem harvested using the 2/4-opposite technique; Su: Useful area; T: Demi-rotation. The average productivity of a stem (R) is as determined by Betti and Ambara (2013); it is equal to 30 kg of dried bark for the 2/4 opposite sides harvesting technic. For carbon stock assessment, the allometric equation developed by Chave et al. (2014) was used for epigenetic biomass estimation:  AGB = exp[-1.803-0.976E+0.976ln(φ) + 2.673ln(D)-0.0299 (ln(D)2] with AGB: estimated epigenetic biomass in kg; E: environmental index that depends on the geographical coordinates of each plot; φ: the specific gravity of the wood in g/cm³; D: diameter at breast height in cm. Thus, the carbon stock (in t C / ha) is deduced from the biomass according to the following formula: (AGBx0.47)/1000 (Zapfack et al., 2013); then it will be converted into ton of carbon per hectare. The graphs and curves were made with Excel 2013, the statistical analyses used are the chi2 test of independence, one-factor ANOVA, and simple linear regressions using R software version 3.3.2.


Sampling effort


The inventory conducted required 3 production teams. A production team is the one which combines both lining and counting. Each team is composed of six members including 1 GPS operator, 2 botanists, 2 macheters, and one secretary. The three teams counted P. africana trees on 23 km for an average sampling effort of 1.9 ≈ 2 km per day per team (Table 1). Twenty-four forest galleries were inventoried by the teams in the four selected villages. A total of 115 plots were delimitated and inventoried, representing a sampling area of 57.5 ha and a sampling rate of 0.72%. The observation made is that the final sampling rate is somewhat different from the theoretical sampling rate designed in advance. Table 2 gives the overall results from the implementation of the sampling design.           


Structural features


Stem density


Table 3 presents the densities of P. africana stems counted by locality/village. The average density of all villages is 6.23 stems/ha. The density of harvestable stems is 4.8 stems/ha. The sites with the highest density of harvestable stems were Hore Garba (6.93 stems/ha), Foungoi (5.16) and Yangaré (4.61). The total basal area of the Mbabo forest is 57.35 m2/ha. The most covered locality is Yangaré (21.31 m2/ha) and the least covered is Botendji (1.74). The average basal area per stem is 0.16 m2/ha. Figure 3 shows that basal area increases with tree size (diameter at breast height) and not with stem density per unit area.



Distribution of P. africana stems by diameter class


The distribution of the 358 stems recorded by diameter class is illustrated in Figure 4. The general shape of the distribution of the species is bell-shaped with a modal class located in the 30-39 cm range, indicating a limited renewal capacity of the species. Note the presence of a few young stems (10-20 cm in diameter) which are represented  at  7.8% of the total  number.  Ninety-one  stems have a diameter smaller than the minimum exploitability diameter (MED) which is 30 cm.  Those non-harvestable trees represent 25.42%. The average diameter of the stems is 48.17 ± 19.8 cm. The average height of the stems is 7 ± 4.26 m while the average thickness of the bark on the unharvested side is 14.1 ± 4.72 mm. There were significant differences in these three parameters between the four locations with respective probabilities of 5.68E-13, 0.000293 and 0.000224 for diameter, height and bark thickness (Table 4).


Assessment of epigeous carbon stock


The  epigeous  woody  biomass  of  the  Mbabo  forest  is estimated at 1432.75 kg/ha, for an overall epigeous carbon stock (for stems ≥10 cm) of 67.3 ± 0 .0015t C /ha. This corresponds to an estimated financial value of 1,749,800 FCFA/ha (USD 2 859.54).


Response of Prunus trees to harvesting


Harvesting technique


Of the 358 stems counted, 94 have been previously harvested, representing 26.25%. Figure 7 shows that several harvesting techniques have been used, including 1/2 (1 over 2) opposite sides, 1/4 (1 over 4) side, 2/4 (2 over 4) opposite sides, 3/4 (3 over 4) sides and 4/4 (total debarking). The technique known as two quarters (2/4) opposite is the most used (79.65%).


Sanitary state of the stems and mortality rate


The majority of the stems exploited or not is alive with a percentage of 95.53%. The few dead and dying stems represent only 4.47% of the total, i.e. a density of 0.28 stems/ha. Mortality due to exploitation is 1.12%, while mortality induced for all other reasons (natural, bush fire, felling, broken tree) is 2.51%. This results in a global mortality rate of 3.63% (Table 5).




Growth parameters and dynamics


The average annual increment of regenerated bark varies among localities depending on the years of harvesting. The average annual increment is 1.3 mm/year, and the significant difference was noted between the four localities (F value = 3.597; Pr(>F) = 0.0166). The greatest is recorded in Botendji (1.48 mm/year). On the other hand, although Botendji has the highest rate of thickness recovery (70%), there is no general difference between the four localities (F value = 2.365; Pr(>F) = 0.0763) (Table 6). A relationship exists between the thickness of unharvested bark and the diameter at breast high (dhp) (X-squared = 4544.9, df = 4224, p-value = 0.0003206). The average annual increment in unharvested  bark thickness is assessed here on the basis of the ratio: bark thickness by diameter. This shows that for a mature stem, the growth (size) of the unharvested bark is 3.7% of that of the diameter for the same growth period (Table 7). Figure 8 illustrates this relationship. It can be deduced that the growth rate of unharvested bark decreases with the growth in diameter during the same period. This is explained by the exponential equation y = 10.05e-0.209x with a correlation coefficient R2 = 0.9542.



Management measures


Distribution of P. africana according to the elevation and distinction of suitability zones


Figure 5 illustrates the distribution of stems by altitude or elevation class. Most of the P. africana stems are found in the 1700-2100 m altitude classes, representing 90%. Ten percent are between 1500-1700 m and no stems were found above 2100 m. One significant difference is noted (F value = 11.31; P(>F) = 4.19e-07) between these spatial positions of stems in the 4 surveyed localities. The analysis of the distribution of P. africana stems according to their elevation allows to estimate its density by zone including: the low altitude zone (below 1300 m) where the species is almost absent, the altitude zone between 1300 and 1700 m where P. africana exists but at low densities, the zone between 1700 and 2100 m considered as the occupation zone per excellence (high densities) and the zone above 2100 m, marked by the absence of P. africana but colonized most often by grassy meadows Figure 6 illustrates the spatial distribution of P. africana densities in the four villages. The analysis of the distribution of P. africana stems by altitude class makes it possible to propose a map of activities to be carried out specifically in relation to P. africana (Figure 9) in the four altitude zones identified:


1. Altitude zone below 1400 m (the species is almost absent): no activities related to P. africana should be carried out;

2. Zone of altitude between 1400 and 1700 m (the species exists but at low densities): zone with favorable conditions for the development of P. africana which could constitute a favorable area for the establishment of P. africana plantations (agroforestry). There should be no exploitation of natural populations of P. africana in this area;

3. Zone between 1700 and 2100 m (high densities of the species): zone where the bark of P. africana should be harvested in the wild and where agroforestry is still possible, but using enrichment practices;

4. Zone of altitude more than 2100 m (almost null or accidental presence of the species): zone colonized most often by the grassy meadows.





Debarking techniques


Several debarking techniques guarantee the regeneration of the bark after the exploitation. Taking into account the ageing aspect of the stems, the weak regeneration recorded in this massif, for practical reasons on the ground and to facilitate the follow-up of the rotation; two techniques can be proposed to know:


1. Two opposite 1/ 4 or (2/4) for stems between 30 and 70 cm;

2. Four opposite 1/8 or (4/8) for stems over 70 cm




The time required for a second harvest is presented in Table 8. It is obtained from the AAMEr (Average Annual Increase in the Regenerated Bark). To harvest bark from the same strip of regenerated bark at Tchabal Mbabo, it would require an average time of 13.39 years or 14 years. This means that to come back on the same tree but on the remaining opposite side, the harvester will need to wait 6.69 ≈ 7 years, representing the half rotation.


Annual possibility or annual quota (case of localities)


The annual exploitable quota in dry tons of P. africana bark is presented by explored locality in Table 9. This quota is 164.6 tons for the entire Tchabal Mbabo Forest.



Sampling effort


A total of 115 plots were scanned by the inventory teams representing a sampling area of 57.5 ha. The survey rate is 0.72%. The actual sampling data obtained in the field, are somewhat different from the theoretical sampling data designed. This discrepancy is due to the difficulties encountered in the field, the most significant of which are those related to the excessively uneven terrain in some places. Nevertheless, the sampling rate obtained, which is not too far from the 1% proposed by the forest inventory standard (MINFOF, 2019) is still very high, at least time 6 higher compared to similar inventory campaigns conducted in previous years in the same area including the sampling rate of 0.1% realized in 2004 by ONADEF (2005), 0.12% in 2011 by ANAFOR under the ITTO-CITES Program (Akoa et al., 2011b), and 0.04% in 2021 by TRAFFIC International (Hiol Hiol, 2021). At Lume (North Kivu) in the Democratic Republic of Congo, P. africana inventories were carried out at a sampling rate of 1.2


Structural features


The average density of all stems is 6.23 stems/ha. This density is lower than 7.94 stems/ha found in Mbabo (Akoa et al., 2011b), 7.18 found in Bioko Island/Equatorial Guinea (Navarro-Cerrillo et al., 2008; Muñoz et al., 2006) and 7.2 stems/ha in Ethiopia (Chaffey, 1978). However, our density is higher than the 3.43 stems/ha found in Mount Cameroon (Betti et al., 2011). On the other hand, the exploitable stem density is 4.8 stems/ha, which is much higher than 1.79 stems/ha and 2.68 stems/ha obtained respectively at Tchabal Ngandaba and Tchabal Mbabo (Akoa et al., 2011b). This shows that the growth of future stems inventoried in 2011 is effective. The low density of young stems shows that Tchabal Mbabo suffers from regeneration problems. The Prunus basal area is 57.35 m2/ha. The average basal area for a stem is 0.16 m2/ha, which is lower than the 0.94 m2/ha obtained in the Bioko Island (Navarro-Cerrillo et al., 2008). Basal area increases with diameter at breast height, not with stem density. Betti et al. (2021) found for Pericopsis elata that the stand basal area increases with both tree density and diameter at breast high. Contrary to Yankam, (2013) in Mount Cameroon and Ronoh et al. (2018) in South west Mau Forest (Kenya) found an inverted "j" structure, the distribution of the 358 stems surveyed is bell-shaped. This clearly shows that P. africana suffers from some regeneration problems in Mbabo. P. africana is a light demanding tree species. For this reason, the number of small stems is often low in primary or non-perturbed forest, due to the lack of light (Durieu de Madron, Forni and Meok, 1998), which tends to suggest that forest logging can be a tool for sustaining ligh demanding tree species. The very low presence of young stems (10-20 cm in diameter) at 7.8% could be due to the death of shoots by competition linked to the absence of light, or to bush fires. In Gabon, Bayol and Borie (2004) present the bell-shaped as the dominant structure of highland forests. Damage caused to the regeneration of stands can constitute a risk for the future of the sustainability of stands (Ellis and Putz, 2019) because the future of forests depends on adequate and safe natural regeneration (Cruz et al., 2021). These regeneration problems can also be explained by its low rate of propagation by its seeds due to its long flowering cycle and its recalcitrant seeds (Komakech et al., 2020). In Mbabo, the average stem diameter is 48.17 ± 19.8 cm and the average height is 7 ± 4.26 m. These are respectively lower than the 101.17 cm and 23.87 m obtained in Kenya in the South Nandi forest (Koros et al., 2016). Betti and Ambara (2013) obtain an average diameter of 68.07 cm in Mbabo. In Equatorial Guinea (Pico de Basilé and Moca) stems reach 24 m in height (Muñoz et al., 2006). When the trees reached 50 cm in diameter, they reached their maximum height (Namuene and Egbe, 2022). In three Mugaga plantations in Kenya (Nyamai et al., 2015) obtained an average diameter of 34.73 ± 13.51 cm for stem 8.36 ± 1.22 m in height.


In Mbabo, the average thickness of the bark on the unharvested side is 14.1 ± 4.72 mm. This value is high than the 12.03 mm found by Lekefack (2016) in Mount Cameroon. The high value of the thickness of the bark obtained in Mbabo may be link to the presence of frequent bush fires in the area compared to North west and South west regions. Shafer et al. (2015) demonstrated that large bark thicknesses are correlated with the time necessary for Cambium to reach dead temperatures and, thus, constituted a strong predictor of resistance from the rod to the bush fire.


Response of trees to harvesting


In Mbabo, 95.53% of the stems, whether harvested or not, are alive, showing a mortality rate of 3.63%. Stewart (2001) estimated the annual mortality of adult trees in P. africana natural populations at 1.5% in Mount Oku, North west Cameroon. The bush fires is one of the main causes of mortality of P. africana stems in Mbabo area. The exploitation of tree bark very often has a very high impact on biodiversity because an intense exploitation of bark exposes the sapwood to the attacks of pests. This weakens the biological functioning of the tree and can cause their death and this, especially in the rainy season (Bayoi et al., 2021). Across the Mbabo forest, the average annual increment in regenerated bark thickness is 1.3 mm/year, with a significant difference between the 4 localities (F value = 3.597; Pr(>F) = 0.0166). This increment is much higher than the 0.61 mm/year in Kumbo plantations (Betti et al., 2019). However, it is smaller than the 1.85 mm/year found at Mount Cameroon (Lekefack, 2016) and also the 2.15 mm/yr obtained from Fundong plantations (Betti et al., 2019). Interestingly, tree size has an effect on bark recovery rate for P. africana (Momo et al., 2016). Nkeng et al. (2010) found that for the first two years after debarking, increment is 0.15 cm/year and this decreases over time at 0.06 cm/year. Solefack and Kinjouo (2017) show in their study in the South west Cameroon that, the bark levy causes a sharp reduction or a slowdown in the growth in thickness of the rod for the benefit of the renewal of the bark surface taken. The reconstitution rate of regenerated bark in thickness is 60%. This rate of over 50% shows that the species has a great capacity for regeneration. However, this regeneration can be influenced by the harvesting period, the spatial position (altitude) or by the diameter of the tree. According to Momo et al., (2016), the rate of bark recovery is influenced by several factors: season and intensity of landing, tree size and altitude. In the montane southern Cape forests of South Africa, the differences in the regeneration process observed at the levels of species and individuals are associated with the intensity of tissue damage and the cutting season (Beltrán et al., 2021). The correlation between unharvested thickness and diameter shows that the growth rate of unharvested bark is 3.7% of diameter growth. The growth rate of the bark decreases over the years with the growth of the diameter of the tree. The younger is the tree, the more important is the growth rate. Betti et al. (2019) found that the thickness of the bark increases with the diameter of the tree beyond a certain level before it starts decreasing. The average bark thickness varies from one diameter class to another. Changes in diameter classes result in variations in bark thickness of P. africana (Tadjuidje, 2011). Light also could play an important role in this report. It is an environmental factor that influences plant growth because it is a crucial requirement for photosynthesis (Nyamai et al., 2015).


Management measures


Four major zones of variable Prunus density can be identified between 1400 and 2100 m. It is practically in this altitude interval (1400 to 2500 m) that the stems are found in Equatorial Guinea (Navarro-Cerrillo et al., 2008). In Tchabal Mbabo, 90% of P. africana stems are found at altitudes of 1700 to 2100 m (very high density). This can be explained by the fact that it is in this interval where the majority of forest galleries are present, which favors a low temperature climate (favorable environment for the species). In the same line, Awono et al. (2015) stated that the distribution is significantly influenced by altitude, temperatures, rainfall and cloud cover. For the area below 1300 m the temperature is higher, thus not favoring the development of the species. Given these regeneration problems and its low density, it would be interested in turning to the agroforestry or plantations. A study at the center of the Uganda noted that 73% of the population (farmers) around the forests received and granted a favorable opinion to the domestication of the species (Galabuzi et al., 2021). Five harvesting techniques are identified: 1/2, 1/4, 2/4, 3/4 and 4/4. The technique known as two quarters (2/4) opposite sides is the most used (67.8%). This result is close to that of Betti et al. (2019) where six harvesting methods were recorded in northwestern agrosystems. In both of these cases, the 2/4 opposite technique was also the most used. Wete (2022) noted that two legal techniques including 2/4 and 4/8, and two illegal techniques 3/6 and total debarking were used in the Mount Cameroon production site. The so-called legal techniques resulted in the death of 4.12% of stems and the decline of 20.58% of stems. In the North-west Region, three harvesting techniques were identified in community forests and six techniques in agroecosystems. This observation of several harvesting techniques may be justified by the incompetence of the harvesters, or by their desire to increase the amount of the bark harvested in order to earn more money. However, precious efforts have been made to establish good standardization, as well as specific guidelines for good practices of harvesting medicinal plants (Pandey and Das, 2013). Betti et al. (2016) reveal during a socioeconomic study in Mount Cameroon and the state of the exploitation measures of Prunus africana in the South west that operators do not regularly apply the recommended methods because of the very damaged relief for some and the price per kilometer very low for others. Geudje et al. (2016) evaluated the capacity of Garcinia kola trees to regenerate their bark after the harvest. A debarking species can survive if it can overcome the trauma of the targeting and develop new tissues (hardening and thickening of the epidermis) which allow it to ensure its survival (Solefack and Kinjouo, 2017). The rate of stand recovery is influenced by the natural diametric growth rate of the tree. During a half rotation there are stand dynamics, including stem recruitment and bark growth. If stem recruitment is not high, this will have a negative impact on the harvestable quota for the new half rotation. Wete (2022) obtained an annual diameter increment for P. africana of 0.42 cm/year in Mount Cameroon. For plantations in the Northwest the increment is 0.91 cm/year (Betti et al., 2019). Bark regrowth is more reliable and accurate in some areas with favorable climatic conditions than others (Cunningham et al., 2016). However, aside from environmental conditions, poor harvesting practice could increase mortality rate or diameter growths, which are also key factors in recovery/recruitment. Damage to young trees has a long -term impact on the regeneration process (Danilovi? et al., 2015), and diameter growth can be reduced by 10 to 20 % due to surface injuries (Yilmaz and Akay, 2008). Using the productivity of a stem which is 30 kg (Betti and Ambara, 2013), the annual exploitable quota of dry matter of P. africana bark is 164.6 tons for the 8 000 ha of useful forest delimitated in the four villages inventoried. This represents about 0.021 tones/ha. This quota could be important if the useful area was even greater. But Bodeker et al., (2014 notes a great decrease in the geographic distribution in sub -Saharan Africa of this species of canopy caused by farming, slash-and-burn agriculture and the construction of habitats. This is also the case with Tchabal Mbabo. All the same, this quota is higher, times 8 than the 473.245 tons obtained on 120 994,08 ha for a half rotation of 5.5 years in Mbabo in 2011 by ANAFOR (Akoa et al., 2011b) and which represents 0.003 tons/ha for the same half rotation (7 years).  This could be explained by the fact that our inventory focused on sites indicated by local people as production sites of P. africana.  


Forest inventories conducted in the Mbabo forest reveal that P. africana has a good stem density (6.23 stems/ha) with a basal area of 57.35 m2/ha. The average bark thicknesses are 14.1 ± 4.72 mm and 10.39 ± 4.22 mm for the unharvested and harvested sides respectively. The annual bark growth is 1.3 cm/year for a recovery rate of 60%. The surveys and forest inventories conducted have made it possible to estimate a first annual exploitation quota for P. africana of 164.6 tons/year in Tchabal Mbabo for a half rotation of 7 years. This quota is to be harvested from a useful area of 8000 ha between the altitudes of 1700 and 2100 m. This massif suffers from regeneration because young trees are not very abundant. Agroforestry would be beneficial for this forest in areas where the species is present but at low density to increase its potential, at the altitude 1 300-1 700 m to be precise.


The authors have not declared any conflict of interests.


This work was carried out within the frame of the project "projet de plan d'action et d'actualisation de l'avis de commerce non prejudiciable en vue de la gestion durable de Prunus Africana (Rosaceae), espece d'arbrelistee en annexe ll de la CITES au Cameroun" of the CITES Endangered Tree Species Program (CTSP) coordinated by the CITES Secretariat General and funded by the European Union Commision. The University of Douala, local communities, AFRIMED and SGP leaders for allowing them use their facilities, for their active participation, advices and cooperation.


Akoa A, Betti JL, Ewusi NB, Mbarga N, Akagou ZHC, Fonkoua C, Essomba ER, Nkouna AC (2010). Preliminary report on sustainable harvesting of Prunus africana (Rosaceae) in the North West region of Cameroon. Report prepared for the national forestry development agency (ANAFOR), the Cameroon CITES scientific authority for flora, in the frame of the project "non-detriment findings for Prunus africana (Hook.f.) Kalman in Cameroon". P 72.


Akoa A, Betti JL, Ewusi NB, Mbarga N, Akagou Zedong HC, Fonkoua C, Mala AW, Nkouna AC (2011a). Preliminary report on sustainable harvesting of Prunus africana (Rosaceae) in the mounts Tchabal Gang Daba and Tchabal Mbabo, Cameroon. Report prepared for the National Forestry Development Agency (ANAFOR), the Cameroon CITES Scientific Authority for flora, in the frame of the project"Non-detriment findings for Prunus africana (Hook.f.) Kalman in Cameroon". P 37.


Akoa A, Betti JL, Ewusi NB, Mbarga N, Akagou Zedong HC, Fonkoua C, Mala AW, Nkouna AC (2011b). Preliminary report on sustainable harvesting of Prunus africana (Rosaceae) in the mounts Tchabal Gang Daba and Tchabal Mbabo, Cameroon. Report prepared for the National Forestry Development Agency (ANAFOR), the Cameroon CITES Scientific Authority for flora, in the frame of the project "Non-detriment findings for Prunus africana (Hook.f.) Kalman in Cameroon". P 25.


Awono A, Tchindjang M, Levang P (2015). Etat des lieux de la filière écorce de Prunus africana : cas des regions du Nord-Ouest et Sud-Ouest du Cameroun. Available at:



Bayoi EA, Menyene EF, Mouyakan AME, Ngaba MJY (2021). Amenagement des produits forestiers ligneux et non ligneux dans la region de l'Est-Cameroun: Cas de la station polyvalente de recherche agricole d'Abong Mbang. Journal of the Cameroon Academy of Sciences 17(1):14.


Bayol N, Borie JM (2004). Itinéraires techniques d'aménagement des forêts de production en Afrique centrale. Bois et Forêts des Tropiques 281(3):15.


Beltrán RL, Valdez HJI, Saynes VA, Blancas J, Sierra HJ.A, Cristians S, Martínez BA, Romero MA, Luna CM, Borja RMA, Pineda HE, Maldonado AB, Angeles PG, Ticktin T, Bye R (2021). Sustaining Medicinal Barks: Survival and Bark Regeneration of Amphipterygium adstringens (Anacardiaceae), a tropical tree under experimental debarking. Sustainability 13(5):2860.


Betti JL, Fouadjo B, Wete E, Ngueguim JR, Njimbam OF, Tientcheu S, Tchiyip PD (2019). Monitoring the harvesting of the barks of Prunus africana (Hook.f.) Kalkman (Rosaceae) in the agroforest systems of North-West region of Cameroon. Available at:



Betti JL, Ambara J (2013). Mass of Prunus africana stem barks on Tchabal mbabo and Tchabal gang daba mountain forests, Cameroon. African Journal of Environmental Science and Technology 7(5):19.


Betti JL, Belinga SJ, Samba D (2011). Stock of Prunus africana stems on the Mount Cameroon forest. African Journal of Plant Science 5(12):10.


Betti JL, Kemkeng F, Ngueguim JR, Ambara J, Njimbama NFO (2021). Effect of thinning on Pericopsis elata (Harms) Meeuwen (Fabaceae) found in forest plantations in the East and South regions of Cameroon. Journal of Plant Studies 10(1):1-15.


Betti JL, Ngankoue MC, Njimbam NFO, Wete E (2016). Monitoring the implementation of Prunus africana (Rosaceae) management plans in Cameroon: respect of norms. African Journal of Plant Science 10(9):172-188.


Bodeker G, Klooster VTC, Weisbord E (2014). Prunus africana (Hook.f.) Kalkman: the overexploitation of a medicinal plant species and its legal context. The Journal of Alternative and Complementary Medicine 20(11):810-822.


Chaffey DR (1978). South-west Ethiopia forest inventory project. An inventory of Tiro Forest.


Chave J, Réjou?Méchain M, Búrquez A, Chidumayo E, Colgan MS, Delitti WB, Vieilledent G (2014). Improved allometric models to estimate the aboveground biomass of tropical trees. Global Change Biology 20(10):3177-3190.


Cruz DC, Benayas JMR, Ferreira GC, Santos SR, Schwartz G (2021). Un aperçu de la perte et de la restauration des forêts en Amazonie brésilienne. Nouvelles Forêts 52:1-16.


Cunningham AB, Anoncho F, Sunderland T (2016). Power, policy and the Prunus africana bark trade, 1972?2015. Journal of Ethnopharmacology 3(178):23-33.


Cunningham AB, Ayuk E, Franzel S, Duguma B, Asanga C (2002). An economic evaluation of medicinal tree cultivation Prunus africana in Cameroon. People and Plants Working 10:35.


Cunningham AB, Mbenkum FT (1993). Sustainability of harvesting Prunus africana bark in Cameroon: a medicinal plant in international trade. pp. 1-28.


Danilovi? M, Dragan DP, Stojni? D, Antoni? SK (2015). Dommages aux arbres résiduels et régénération lors de l'abattage et de l'extraction du bois dans les peuplements de hêtres mixtes et purs. Liste Sumarski 5-6:253-262.



Dawson I, Rabevohitra R (1996). Survey report: status of Prunus africana resources in Madagascar Unpublished Survey Report Prepared for the International Centre for Research in Agroforestry. Nairobi, Kenya.


Diarra MD (2006). Etude de la phytochimie et des activités biologiques d'une recette traditionnelle utilisée dans le traitement de l'hypertrophie bénigne de la prostate au Mali. Thèse pour obtenir le grade de docteur en Pharmacie (Diplôme d'état) Faculté de Médecine de Pharmacie et d'Odonto - Stomatologie. P 138.


Durieu De Madron L, Fomi L, Meok M (1998). Les techniques d'exploitation à faible impact en forêt dense humide Camerounais. Cirad, document Forafri. P 30.


Ellis P, Putz FE (2019). Introduction au numéro spécial : Exploitation forestière à impact réduit pour l'atténuation du changement climatique (RIL-C). Écologie et gestion forestières 437:396-410.


Fagny AM, Nkouandou OF, Bardintzeef JM, Temdjim R, Guillou H (2017). Pétrologie du volcanisme Eocène-Oligocène du massif de Tchabal Mbabo, Adamaoua-Cameroun, Afrique central. Afrique SCIENCE 12(6):35-47.


Galabuzi C, Agaba H, Eilu G (2021). Farmers' perceptions, socio?economic and political stakes: What inspires the integration of Prunus africana on?farms in central Uganda? Small-Scale Forestry 20(3):371-389.


Guedje NM, Tchamou N, Lejoly J (2016). Tree response to bark harvest: the case of a medicinal species, Garcinia lucida, as source of raw materials for plant-based drug development. Journal of Applied Biosciences 99:9476-9491.


Herrmann HW, Schmitz A, Herrmann PA, Bohme W (2007). Amphibians and reptiles of the Tchabal Mbabo Mountains, Adamaoua Plateau, Cameroon. Bonner Zoologische Beiträge 55:27-35.


Hiol Hiol F (2021). Etude de la filière Prunus africana dans la zone de Tchabal Mbabo, Adamaoua, Cameroun. TRAFFIC International. Available at:



Ingram V, Awono A, Schure J, Ndam N (2009). Guidance for a national Prunus africana management plan, Cameroon. CIFOR, FAO, 158.


Komakech R, Kim YG, Kim WJ, Omujal F, Yang S, Moon BC, Okello D, Rahmat E, Kyeyune GN, Matsabisa MG, Kang Y (2020). A micropropagation protocol for the endangered medicinal tree prunus africana (hook f.) kalkman: genetic fidelity and physiological parameter assessment. Frontiers in Plant Science 11:548003.


Komakech R, Kang Y, Lee JH, Omujal F (2017). A review of the Potential of Phytochemicals from Prunus Africana (Hook f.) Kalkman Stem Bark for Chemoprevention and Chemotherapy of Prostate Cancer". Evidence-Based Complementary and Alternative Medicine 2017:10.


Koros KH, Konje MM, Wambua MM, Chesire CK, Odeny D (2016). Population Status And Conservation Hotspots Of Prunus Africana (Hook.F.) Kalkman In South Nandi Forest, Western Kenya P 14.


Lekefack LF (2016). Evaluation du taux de reconstitution de l'écorce du Prunus Africana (Hook.F.) Kalkman après exploitation dans le parc national du mont Cameroun. Mémoire présenté en vue de l'obtention du diplôme d'ingénieur de conception des eaux, forêts et chasses. Université de Dschang. P 77.


Lehmann H (2013). Le médicament à base de plantes en Europe : statut, enregistrement, contrôles. Droit. Université de Strasbourg, 2013. Français. ffNNT: 2013STRAJ024ff. fftel-00936734ff. Thèse de Doctorat. Available at.



MINFOF (2019). Directives d'inventaires d'aménagement et de préinvestissement integrant les spécificites de biodivesrité. P 68.


MINFOF (2018). Suivi de la mise en œuvre des plans de gestion du Prunus africana dans la région de l'Adamaoua. pp.46. Available at:



MINEF (2001). Procédure d'élaboration, d'approbation, de suivi et de contrôle de la mise en œuvre, des plans d'aménagement des forets de production du domaine forestier permanent (Arrete 222). P 18.


Momo SMC, Nguetsop VF, Dongmo NJ, Kenguem KG, Avana TML (2016). The Effect of Some Ecological and Anthropic Factors on the Survival and Bark Recovery Rate of Prunus africana (Rosaceae) in South-West, Cameroon P 8. Available at:



Muñoz C, Cerrillo NMA, Kasimis RM, Bermejo HN, Cedrés PJE, Fernández EMC, Clemente EH, Porras ARG (2006). Evaluation of the harvest of "Prunus Africana" bark on Bioko (Equatorial Guinea): guidelines for a management plan. Université de Córdoba. P 168. Available at:



Mutuma GG, Joseph N, King'ori MA, Silas K (2020). Phytochemical and anti-inflammatory analysis of Prunus africana bark extract. Research Journal of Pharmacognosy 7(4):31-38.


Namuene K, Egbe A (2022). Impact de l'exploitation forestière sur les peuplements voisins dans une forêt du sud-ouest du Cameroun. Open Journal of Forestry 12:248-262.


Navarro-Cerrillo RM, Muñoz MA, Alfonso PGA (2008). Setting export quotas of Prunus africana: Guidelines for a Management Plan Key questions. Workshop on Implementation of Review of Significant Trade (RST) Recommendations for Prunus africana Naivasha, Kenya. Spain: University of Córdoba. Available at:



Nkeng PF, Ingram V, Awono A, Tientcheu MLA (2010). Assessment of Prunus africana bark exploitation methods and sustainable exploitation in the South west, North-west and Adamaoua regions of Cameroon. Project GCP/ RAF/408/EC. Mobilisation et Renforcement des Capacités des Petites et Moyennes Entreprises impliquées dans les Filières des Produits Forestiers Non Ligneux en Afrique Centrale. CIFOR. Yaoundé: FAO CIFOR-SNV-World Agroforestry Center-COMIFAC. P 57. Available at:



Nyamai DW, Arika WM, Rachuonyo HO, Wambani JR, Ngugi MP (2016). Herbal management of benign prostatic hyperplasia. Journal of Cancer Science and Therapy 8(5):130-134.


Nyamai DW, Mawia AM, Wambua FK, Abdirahman YA, Osano K, Lagat R, Mumbi B, Arika W, Juma KK, Anyango E, Mulugeta M, Ngugi MP, Muchugi A, Ng'ang'a M, Burugu MW (2015). Growth performance of domesticated Prunus africana population in Muguga, Kiambu County, Kenya. Biochemistry Physiology 4(4):185.


Ochwang'i DO, Kimwele CN, Oduma JA, Gathumbi PK, Mbaria JM, Kiama SG (2014). Medicinal plants used in treatment and management of cancer in Kakamega County, Kenya. Journal of Ethnopharmacology 151(3):1040-1055.


ONADEF (2005). Evaluation des ressources forestières nationales du Cameroun. Résultats de l'Inventaire Forestier National P 26.


Pandey AK, Das R (2013). Good field collection practices and quality evaluation of medicinal plants: Prospective approach to augment utilization and economic benefits. Research Journal of Medicinal Plant 8(1):1-19.


Randriambololona DJ (1994). Analyse de l'exploitation de Pygeum africanum. Mém de Fin d'Études en vue de l'obtention du CAPEN, École Normale Supérieure, Antananarivo. P 77.


Rasoanandrasana R (2010). Techniques pour la culture aseptique initiale de Prunus africana Hook.f (Kalkman, 1965). Mémoire d'obtention du Diplôme d'Etude Approfondie en Biologie et Ecologie Végétales, option: Physiologie Végétale. Université d'Antananarivo. P 72. Available at:



Ronoh DK, Sirmah PK, Hitimana J, Mullah CJA (2018). Variation in regeneration density and population structure of Prunus africana across human disturbance gradient in South West Mau Forest, Kenya. International Journal of Natural Resource Ecology and Management. 3(1):1-8.


Shafer JL, Breslow BP, Hohmann MG, Hoffmann WA (2015). Relative bark thickness is correlated with tree species distributions along a fire frequency gradient. Fire Ecology 11:14.


Shenouda NS, Sakla MS, Newton LG, Besch WC, Greenberg NM, MacDonald RS, Lubahn DB (2007). Phytosterol Pygeum africanum regulates prostate cancer in vitro and in vivo. Endocrine 31(1):72-81.


Simons AJ, Dawson IK, Duguma B, Tchoundjeu Z (1998). Passing problems: prostate and Prunus. Herbalgram 43:49-53.


Solefack MCM, Kinjouo GK (2017). Modifications anatomiques après écorçage de trois espèces au Sud-ouest Cameroun. Journal of Applied Biosciences 115:11490-11501.


Stewart KM (2001). The commercial bark harvest of the African cherry (Prunus africana) on Mount Oku, Cameroon: effects of traditional uses and population dynamics. PhD thesis, Florida International University. Available at:



Sven W, Rakotonirina JCR (1995). L'exploitation de Prunus africana à Madagascar. Rapport élaboré par le PCDI Zahamena et la DEF Antananarivo/Fénérive-Est.


Tadjuidje E (2011). Contribution à la gestion durable de Prunus africana (hook.f.) kalkman: phénologie et régénération naturelle en plantation et en forêt naturelle. Mémoire de Maîtrise «Faculté d'Agronomie et des Sciences Agricoles» de l'Université de Dshang. Available at:




Tewari VP (2016). Forest inventory, assessment, and monitoring, and longterm forest observational studies, with special reference to India, Forest Science and Technology 12(1):24-32.


Tonye M, Stella A, Ndam N, Blackmore P (2000). State of knowledge of Prunus africana (Hook. f.) Kalkman. Report established for Central Africa region at program for the Enviroment (CARPE). Washington Dc. Available at:



Usongo L (2019). Redeeming the Lost Conservation Pearl of Adamawa highlands Cameroon Tchabal Mbabo P 2.


Vivien J, Faure JJ (2011). Arbres des forêts denses d'Afrique centrale. Saint Bathevin (France). P 974.


Wete E (2022). Gestion durable d'un Produit Forestier Non Ligneux au Cameroun (Prunus africana (Hook. F.) Kalkman): mise en œuvre des mesures de l'Avis de Commerce Non Préjudiciable. Thèse présentée en vue de l'obtention du Diplôme de Doctorat/PhD en Biologie. Option: Ecologie, Biodiversité et Environnement. Université de Douala P 253.


Yankam S (2013). Analyse de l'impact de la gestion actuelle de Prunus africana (Hook. F.) Kalkman au Mont Cameroun (Région du Sud-Ouest Cameroun). Mémoire d'Etudes Supérieures Spécialisées (DESS) en Aménagement et Gestion intégrés des Forêts et Territoires tropicaux. Université de Kinshasa. pp 32-38. Available at:



Yilmaz M, Akay AE (2008). Dégâts de peuplement d'un système de coupe de sélection dans une forêt mixte inéquienne de Çimenda?i à Kahramanmaras-Turquie. Journal international des sciences naturelles et de l'ingénierie 2:77-82.


Zapfack L, Noiha NV, Dziedjou KPJ, Zemagho L, Fomete NT (2013). Deforestation and Carbon Stocks in the Surroundings of Lobéké National Park (Cameroon) in the Congo Basin. Environment and Natural Resources Research. Canadian Center of Science and Education 3(2):78-86.