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Research Article
Local perception of the current state and threat factors of a critically endangered species, Celtis toka (Forssk.) Hepper & J.R.I. Wood, in Burkina Faso: implications for species conservation
expand article infoZaïnabou Dabré§, Issouf Zerbo |, Blandine Marie Ivette Nacoulma, Dodiomon Soro§, Adjima Thiombiano
‡ University Joseph Ki-Zerbo, Ouagadougou, Burkina Faso
§ University Félix Houphouët Boigny, Ouagadougou, Burkina Faso
| University Thomas Sankara, Ouagadougou, Burkina Faso
Open Access

Abstract

Celtis toka, the only species of the genus Celtis (family Cannabaceae) encountered in the flora of Burkina Faso, is critically endangered in the country. To engage the public for the future conservation and domestication of the species, knowledge of the factors threatening Celtis toka survival is necessary. Thus, the study objective was to identify the perceptions of local people concerning the current state and conservation strategies of Celtis toka in Burkina Faso.

To investigate potential solutions to the threats posed to Celtis toka, we randomly surveyed 405 consenting participants using a selected semi-structured interview. Moreover, field observations were performed to assess the threat drivers cited by local people of the Sudanian and Sudano-Sahelian climatic zones. Descriptive analyses (relative frequency and fidelity level) and generalized linear models (GLMs) were used to highlight the impact of sociodemographic factors and climate zones on the current state, threat drivers, and potential solutions. The chi-square test was used to assess whether to plant C. toka.

GLM analyses revealed that local knowledge about the current state, threat factors and potential solution to the threat as related to natural stand varied significantly according to ethnolinguistic group (P < 0.000), sex (P = 0.01) and age (P = 0.01). Rural people had varying perceptions of the current state of C. toka. Sixty-eight percent reported a decrease in population, ten percent reported scarcity, and five percent reported extinction. The views of local people were that the factors affecting C. toka were pruning (25%), climate change (14%), deforestation (10%), ageing (10%), debarking (9%), and agriculture (7%). Potential solutions included planting (45%), conservation of C. toka and its habitat (27%), sustainable use of Celtis toka (14%), promotion of education and awareness about Celtis toka (10%) and tree/crop association (5%).

The study concluded that the ethnobotanical knowledge of Celtis toka may play an important role in its conservation and domestication in Burkina Faso. Furthermore, its incorporation into reforestation and restoration programs is critical to species survival.

Keywords

climate, conservation strategies, COVID-19, decline, ethnobotany, extinction, West Africa

Introduction

Climate change is defined as a change in the weather pattern of a location or region that is related to average weather components such as temperature, wind patterns and precipitation (Ifeanyiobi et al. 2012). For instance, extreme weather events devastate the land and terrestrial ecosystems and exacerbate food insecurity for humanity. These changes, according to the United Nations’ Intergovernmental Panel on Climate Change, have a large impact on many people who are thought to be disproportionately vulnerable to the effects of climate change (IPPC 2021). To cope with global change and mitigate its consequences, rural communities rely on forests, primarily in terms of multipurpose plants for medicine, food, fodder, shade, renewable energy, windbreaks, erosion control, carbon sinks, soil improvement, fertility restoration and conservation (Ifeanyiobi et al. 2012).

Ethnobotany, a branch of ethnobiology (Houéhanou et al. 2016), is the study of the relationships between plants and culture as well as the local perception of the use, management (Bridges and Lau 2006; de Albuquerque and Hanazaki 2009) and the state of plant resources. Moreover, ethnobotanical knowledge is critical for species conservation, mainly for endangered species that have been recognized by the Convention on Biological Diversity in Rio de Janeiro (CBD 1992). Furthermore, promoting endangered plants is critical to ensuring their sustainable conservation, domestication, and inclusion in reforestation and restoration programs. Therefore, plant promotion, conservation, domestication, and introduction through restoration and reforestation, necessitate a scientific approach based on local perceptions of the current state, threats, and potential solutions.

Celtis toka (Forssk.) Hepper & J.R.I. Wood belongs to the Cannabaceae family. The genus Celtis includes approximately 60–70 species worldwide (Mahre et al. 2017) and 12 species in Africa (Sattarian and Van Der Maesen 2005). This species is a very large tree with a compact crown (Sattarian 2006) and is usually monoecious (Alfaifi et al. 2021). It reaches 25 m in height and 2.2 m in diameter at breast height. The bole is either short or tall with ramifications (Dabré et al. unpublished). Celtis toka (C. toka) is an open gallery forest, dense dry forest, savannah, sacred grove, and rocky area species (Neumann 1992; Shepherd 1992; Rabeil 2003; Akoegninou et al. 2006; Savadogo and Thiombiano 2010; Höhn and Neumann 2016; Arbonnier 2019). It thrives in areas with low rainfall (110–960 mm yr.-1) and high temperatures (26–30 °C) (Watrin et al. 2007). It is widely distributed and found throughout Benin, Burkina Faso, Central African Republic, Chad, Côte d’Ivoire, Eritrea, Ethiopia, Gambia, Ghana, Guinea (Conakry), Mali, Mauritania, Niger, Nigeria, Senegal, South Sudan, Sudan, Togo, Uganda, and Yemen (Sattarian 2006; IUCN 2019).

The species provides a variety of products used for food (leaves, fruit); medicine (leaves, barks, roots, flowers, seeds); construction (wood); firewood and charcoal for human cooking activities; and fodder (leaves) for animals and handicrafts (Blench 2000; Lykke et al. 2004; Teklehaymanot and Giday 2010; Seignobos 2014; Höhn and Neumann 2016; Piqué et al. 2016; Arbonnier 2019; Badiane et al. 2019). The fruits and leaves are considered edible in Sudan (Arkell 1947), Ghana (Irvine 1961), Senegal (Lericollais 1990), Nigeria (Kiee et al. 2000; Harris and Mohammed 2003; Kubmarawa et al. 2011), Cameroon (Nakagawa 2008; Neba 2009; Betti and Yemefa 2011), Benin (Djègo-Djossou et al. 2015) and Burkina Faso (Dabré et al. unpublished). Mballow et al. (2020) stated that C. toka is the most commonly used species by communities in west and east Africa. Moreover, tannins, glycosides, alkaloids, saponins, phenols, coumarins, flavonoids, mucilage, triterpenoids and steroids are phytochemicals extracted from leaves of C. toka (Fall et al. 2017; Abba Idris and Halima Mohammed 2020).

In addition, all organs of C. toka are used to cure diseases such as measles, chickenpox, malaria, back and eye aches, ringworm, fever sore, mycosis, headache, and mental diseases (Hahn-hadjali and Thiombiano 2000; Betti et al. 2011; Arbonnier 2019; Diatta et al. 2019). The roots, leaves and bark are used in Nigerian traditional medicine to treat various diseases, including epilepsy (Muazu and Kaita 2008). Additionally, the plant organs are used to treat trypanosomiasis (Osue et al. 2018). In Cameroon, the bark is also used to cure epilepsy (Tsabang et al. 2016). The medicinal use of C. toka was also highlighted by Bizimana et al. (2006) in Mali and Badiane et al. (2019) in Senegal. In Burkina Faso, leaves, bark, flowers, fruits, grains, and roots were used to heal 29 ailments, such as madness, yellow fever, eye ache, malaria, casting, vitamin deficiency, ringworm, diarrhea, backache, toothache, ulcer, measles, and chickenpox (Dabré et al. unpublished).

In Ethiopia, C. toka is a wild tree that provides an important economic service because it is preferred for the hanging of beehives (Bareke 2018), for timber, and for making local boats (Rolkier and Abebe 2015). In addition, C. toka has a mystical value in Burkina Faso (Savadogo and Thiombiano 2010). Cultural and mystical values were also highlighted by Dabré et al. (unpublished).

The International Union for Conservation of Nature (IUCN)’s forest work addresses the role of trees and forests in building resilience to climate change (IUCN 2021). Additionally, the IUCN sustainable use initiative has been successful in delivering conservation outcomes that benefit society (IUCN 2020). C. toka was assessed on the IUCN Red List of Threatened Species in 2023 as being of Least Concern (LC), and its current population trend is stable at present (IUCN 2019, accessed on January 25, 2023). According to the IUCN (2019), C. toka has a very broad distribution and a large population, with no major threats currently existing and no significant future threats being identified.

Even though C. toka is classified as LC at the global level (IUCN 2019), this species is either threatened, rare, critically engendered and even extinct in some temperate regions and the Sahelian region in Africa (Hahn-hadjali and Thiombiano 2000; Garzuglia 2006; Al-Khulaidi 2018; Alfaifi et al. 2021; Tchobsala et al. 2022). Nonetheless, the species seems to be lacking in Senegal, Guinea Sudan, and Uganda (Hauman 1942). Moreover, C. toka is threatened in Benin, northern Cameroon and the Sahelian region of Africa (Gonzalez et al. 2012; Dansi et al. 2013; Moksia et al. 2019). In Chad, the species is either extinct or endangered (Tchobsala et al. 2022). Although the species is important in Yemen, it is currently rare and must be evaluated and monitored regularly (Al-Khulaidi 2018). In Saudi Arabia, C. toka is thus a very rare and threatened species (Alfaifi et al. 2021). The reasons for the rarity and near local extinction of this species in some parts of Africa are understandable. This is because of the enormous dependency on this species and its products for ecological and economic purposes in some parts of African countries. This, leads to overexploitation, thus predisposing the species to a high risk of local extinction in Africa. This phenomenon is prevalent in west Africa, especially Burkina Faso, where the species is subject to overexploitation because of its medicinal, fodder, food, and mystical uses (Dabré et al. unpublished).

Only C. toka, one of the twelve species of the genus Celtis in Africa, is found in Burkina Faso, and it is on the verge of extinction. Several pieces of empirical evidence suggest that C. toka is rare, threatened, critically endangered or extinct in Burkina Faso. Authors have shown that in Burkina Faso, C. toka is a one-of-a-kind critically endangered species (Garzuglia 2006) and is threatened to the point of one day disappearing (Hahn-hadjali and Thiombiano 2000; Thiombiano et al. 2010; Bayala et al. 2011). Vodouhe et al. (2007) also stated that C. toka has been on the verge of extinction in Burkina Faso since 2007. For instance, Hahn-hadjali and Thiombiano (2000) also stated that since 2000, C. toka has disappeared in eastern Burkina Faso, except in sacred groves. Furthermore, Bayala et al. (2011) discovered that C. toka was the most threatened species in the agroforestry parkland of Burkina Faso. Additionally, Savadogo and Thiombiano (2010) specified that the wild plant C. toka is endangered in the Northern and Southern Sudanian zones of Burkina Faso. More recently, the studies of Savadogo et al. (2017) have shown that C. toka is rare in the communities of the strict Sahelian, southern and northern Sahelian regions of Burkina Faso. Therefore, given the socio-economic and ecological importance of C. toka to the teeming African populace, and given its potential high risk of local extinction in Africa, there is a need for its conservation. However, an effective conservation strategy of the natural resources must take into account the knowledge and opinions of the stakeholders, especially the local people who are the direct beneficiaries of the resources so conserved (Amoutchi et al. 2021). These authors argued that indigenous people all over the world have preserved distinctive understandings, rooted in cultural experience, that guide relationships among human and non-human beings in specific ecosystems. Thus, their perception and knowledge of threats to any natural resources, and their subsequent contribution to designing a conservation action will produce a positive outcome. The local people (especially in Burkina Faso) depend directly on the services provided by C. toka for their livelihoods. Therefore, they are expected to be the most affected if the species becomes extinct, and also, they are expected to be well aware of the nature of the disturbances and threats the species is facing given their indigenous knowledge of it. Their perception of the threats (the impact and causes) and knowledge of anthropogenic activities impacting this species, being part of their indigenous knowledge, are essential for making and implementing decisions and policies related to the mitigation of these threats, and the management of this species in the ecosystem. Furthermore, the knowledge and perception of the local people represent the baseline information for motivating and directing any research projects regarding any conservation action targeted at this species.

Despite its socioeconomic and cultural importance and its role in mysticism, knowledge of the threat factors of C. toka in Africa in general and Burkina Faso, in particular, is lacking. In this regard, this study aimed to assess the diverse local knowledge and perceptions of the dynamics and threats to C. toka in west Africa (using Burkina Faso as a case study), with the view to recommending conservation strategies to mitigate the local extinction of this species in west Africa where the species is already reported to be critically endangered. Specifically, we seek to answer the following questions: (a) What are the perceptions of rural people regarding the status of C. toka in Burkina Faso? (b) What are the threats to the survival of C. toka in Burkina Faso? And (c) what are the perceptions of the local population concerning the potential solutions to the threats posed to C. toka in Burkina Faso?

We explicitly tested three hypotheses:

  1. Interviewees perceived the extinction of C. toka in the study sites.
  2. Anthropogenic activity is the main driver of species decline.
  3. Planting and the conservation of the species and its habitat are two of the most important solutions to the threats posed to the species.

Description of the study site

This study was conducted from November 2020 to January 2022 in villages near Kou, Dinderésso, Sourou, Sâ and Koulbi classified forests located in the Sudanian and Sudano-Sahelian climatic zones of Burkina Faso (Fig. 1). In both climatic zones (BCZ), the climate is tropical with two separate seasons: rainy and dry periods. The principal rivers are Kou and Mouhoun, and the main soils are leptosols, vertisols, ferralsols, luvisols, lithosols and hydromorphic soils (Savadogo and Thiombiano 2010). The vegetation types include various savannahs, dry forests, and gallery forests.

Figure 1.

Localization of the study sites in Burkina Faso. (Studied PAs: studied protected areas).

The flora consists of some Sahelian, Sudanian and Guinean species, such as Vitex chrysocarpa Planch, Antiaris africana Engl., Parkia biglobosa (Jacq.) R.Br. ex G. Don, Lannea microcarpa Engl. & K. Krause, Dialium guineense Willd., Cola laurifolia Mast., Carapa procera DC., Vachellia seyal (Delile) P.J.H Hurter, Detarium microcarpum Guill. & Perr., Balanites aegyptiaca Del. (Nacoulma et al. 2018). The sociolinguistic groups are Dafing, Gourmantché, Gourounssi, Bobo, Bozo, Dioula, Sambla, Senoufo, Bambara, Marka and Bwaba. The key livelihoods are traditional subsistence farming, principally of cereals (millet, sorghum, and maize), livestock breeding and trade.

Materials and methods

Materials

Celtis toka is a wild plant that thrives in a variety of environments. It has different local names around Africa (Table 1).

Table 1.

Some local names of Celtis toka in Africa.

Countries Dialect Vernacular names Sources
Benin Dendi Séékossou Dansi et al. 2013
Yoruba Afoufè Djègo-Djossou et al. 2015
Bousamsambou Achigan-Dako et al. 2010
Burkina Faso Mooré Pargandé Thiombiano et al. 2012
Mooré Silsaka Thiombiano et al. 2012
Cameroon Arabe Ngouso Betti and Yemefa 2011
Aboum gatou Vivien 1990
Hala
Fulfuldé Djiho
Haoussa Douki
Toupouri Likan
Loubour
Kanouri Ngouzo
Mofu Sabak
Mafa Shéshébé
Wanka
Fulfuldé Ganki Gilbert et al. 2019
Fulfuldé Wanko Gilbert et al. 2019; Seignobos and Tourneux 2002
Mofou Mebed Gilbert et al. 2019
Arabe Falmaro Betti et al. 2011
Ethiopia Anywaa Laero, Awas 1997
Kara (people) Zuguay, Teklehaymanot and Giday 2010
Kwego (people) Lompo Teklehaymanot and Giday 2010
Nigeria Aápe Ogungbenro et al. 2018
Mali Kamaua, Gamya Bizimana et al. 2006
Senegal Wolof Mbul Gonzalez 2001
Diola Busingilit Diatta et al. 2019
Sereer ngan Lericollais 1990
South Sudan Mabanese Shaw Bloesch 2014
Arabe Tekey Bloesch 2014
South Kordofan Sudan Mohagria Ismail and Elawad 2015
Sudan Mohagria, Lipingo Hamid and Kordofani 2015

Methods

Sampling strategy and data collection

A preliminary assessment was carried out in November 2020 to obtain an overview of the availability and distribution of C. toka. Furthermore, this assessment allowed us to obtain approval from authorities and village leaders, as well as to fine-tune the questionnaire. The preliminary assessment and survey were carried out while maintaining social distancing and other preventive measures (wearing a nose mask and using hand sanitizer) to avoid the spread of COVID-19. From the three climatic zones of Burkina Faso, two climatic zones (the Sudanian climatic zone (SCZ) and the Sudano-Sahelian climatic zone (SSCZ)) were chosen considering the accessibility of the areas and the occurrence of C. toka. A discussion was held with the administrators, environmental officers, forest officers, farmers, fishermen/women, hunters, traditional healers, and elders. Next, field observations were made cooperatively with field guides, farmers, village leaders and elders to look for C. toka availability, accessibility, distribution, threat drivers and potential solutions within the study sites. Thirty-four villages were included in the survey, comprising twenty-five ethnolinguistic groups (Fig. 2).

Figure 2.

Map of the ethnolinguistic groups questioned in the study areas.

The ethnolinguistic groups Bambara and Bozo represent immigrants from Mali.

Villages were chosen based on the presence of the multipurpose species C. toka. Overall, 405 (148 female and 257 male) consenting local people who knew C. toka were randomly selected. Data were collected using a selected semistructured interview (Sop and Oldeland 2011; Theodory 2016) and direct field observation. It was impossible to interview an equal sex ratio in each village because the investigations were based on the knowledge of C. toka. All respondents were at least 30 years old because they were the only ones who knew about C. toka and its status. Data for age, sex, career, education level and ethnolinguistic group of the informants were recorded. Ethnolinguistic groups that were represented by few individuals were classified as “other” for the purpose of performing the statistical analysis. Proficient local translators were used to translate French into the local languages.

Photographs of the leaves (Fig. 3), the trunk (Fig. 4), and the fruits (Fig. 5) of C. toka were taken during the prospection, kept, and shown to each household in both climatic zones to ensure that local communities were familiar with C. toka (Arbonnier 2019). The respondents were questioned about the following:

Figure 3.

Pictures of leaves used for quick identification by local people during the survey. Pictures: Z. Dabré, 2020.

Figure 4.

Pictures of the trunks used for quick identification by local people during the survey. Pictures: Z. Dabré, 2020.

Figure 5.

Pictures of fruits used for quick identification by local people during the survey. Pictures: Z. Dabré, 2020.

  • current state of C. toka in their community,
  • factors affecting C. toka survival,
  • potential solutions to the threat.

Data analysis

Before the analyses, the interviewees were divided into two generations: adults (30–55 years) and older adults (≥ 55 years) (Sop et al. 2012). Three and four Sudanian and Sudano-Sahelian ethnolinguistic groups, respectively, were considered major ethnolinguistic groups, with the remainder classified as “other” (Fig. 2, Table 3).

The relative frequency and fidelity level (Table 2) were employed to analyse the most destructive threats to C. toka. GLMs with Poisson errors and chi-square tests at a threshold equal to 0.05 were used to detect sociodemographic parameter (ethnolinguistic groups, age, and sex) effects on the current state, threat, and potential solutions in the BCZ. Chi-square analysis was also used to determine whether to plant C. toka in the study areas. All statistical analyses were performed using R version 4.1.1 (R Core Team 2021).

Table 2.

Formulas related to relative frequency (RF) and fidelity level (FL).

Index Computation Explanation R
RF = (FC/SF) × 100 Frequency of citation (FC) quoted by a given informant divided by the sum of uses times 100. Measures the ratio of the number of times a use pattern of C. toka appears in the set of overall use patterns. The value ranges from 0 to 100. A
FL = (Ip/Iu) × 100 Number of informants (Ip) connected to a specific use divided by the total number of informants (Iu) times 100. Measures the grade of consensus between informants. FL is significant when this is directly above 5% (FL > 5%). B

Results

Sociodemographic characteristics and local perception of the status of C. toka in Burkina Faso

Sociodemographic characteristics of local populations

In total, 405 people were interviewed in this study, with 203 in the SCZ and 202 in SSCZ (Table 3). Most of the interviewees were male (72.77%), autochthonous (81.19%), and farmers (75.74%) with no formal education (80%). Bozo (8.37%) were immigrants, and those classified as “other” were autochthons (Table 3).

Table 3.

Sociodemographic characteristics of informants and study design.

Demographic parameters Variables Sudanian Sudano-Sahelian
Sex Female 40.95 27.23
Male 59.05 72.77
Total 100 100
Residential status Autochthon 65.02 81.19
Migrant 34.98 18.81
Total 100 100
Ages Adult (30–55) 46.80 58.91
Old (> 55). 53.20 41.09
Total 100 100
Ethnolinguistic groups Bobo 71.44 13.86
Bozo 8.37
Bwaba 31.68
Dafing 23.27
Dioula 10.34
Mossi 12.87
Others 9.85 12.87
Total 100 100
School level None 79.59 74.26
Primary 15.75 21.28
Secondary 4.37 3.47
University 0.29 0.99
Total 100 100
Main activity Farming 61.44 75.74
Trade 21.61 8.91
Breeding 11.65 11.39
Handwork 5.3
Hunt 3.96
Total 100 100

Local perception of the status of C. toka in Burkina Faso

Overall, 68% of informants (77.94% in the SCZ and 58.28% in SSCZ) (Fig. 6) widely expressed that the multiuse species C. toka was greatly decreasing (SCZ: 41% < FL < 90% and SSCZ: 52 < FL < 96) (Table 4). Thirteen percent of the participants expressed that the species is stable. In SSCZ, approximately 19% and 11% of the interviewees confirmed that the sacred tree C. toka was either rare or extinct, respectively. However, 4% of the local people (5.88% in the SCZ and 2.86% in SSCZ) highlighted that the species was increasing in abundance (Fig. 6, Table 4). As the most surveyed communities, Bobo, Bozo, Dioula, Bwaba, Dafing, Mossi, and Dioula represent the ethnolinguistic groups that perceived the most recent status of C. toka in the study areas. Ethnobotanical knowledge of the state of C. toka varied greatly across ethnolinguistic groups. However, Dioula (FL: 90%) and Bobo (FL: 62%), belonging to SCZ, perceived the decline of C. toka. However, in the SSCZ, Mossi (FL: 96%) and Dafing (FL: 81%) reported a decrease in the species. Respondents in the SCZ with an age above 55 years identified more of a declining status of the species than others. Regarding sex, men (SCZ) and women (SSCZ) reported more threatened status based on their traditional knowledge when compared to others. The rarity of the species was perceived by the Bwaba culture (FL: 42%), and extinction features of C. toka were mostly perceived by the Mossi (FL: 35%) and the “other” ethnolinguistic groups (FL: 35%) in the SSCZ (Table 4).

Table 4.

Local knowledge of C. toka in two climatic zones of Burkina Faso.

Criteria /Patterns Variants Sudanian climatic zone Sudano-Sahelian climatic zone
Bobo Bozo Dioula Others Bobo Bwaba Dafing Mossi Others
(n=145) (n=17) (n=21) (n=20) (n=28) (n=64) (n=47) (n=26) (n=26)
F FL (%) F FL (%) F FL (%) F FL (%) F FL (%) F FL (%) F FL (%) F FL (%) F FL (%)
Current state of C. toka Extinct 0 0 0 0 0 0 0 0 1 4 13 20 2 4 9 35 9 35
Rare 2 1 1 6 1 5 1 5 2 7 27 42 2 4 8 31 6 23
Decreasing 90 62 7 41 19 90 21 70 15 54 33 52 38 81 25 96 16 62
Stable 37 26 6 35 1 5 4 20 8 29 5 8 5 11 0 0 1 4
Increasing 10 7 1 6 0 0 1 5 3 11 0 0 2 4 0 0 0 0
ΣF 139 - 15 - 21 - 27 - 29 - 78 - 49 - 42 - 32 -
Threat factors Pruning 56 39 8 47 13 62 13 65 4 14 62 97 33 70 6 23 15 58
Bushfire 20 14 0 0 2 10 1 5 1 4 2 3 7 15 0 0 0 0
Ageing 21 15 2 12 2 10 1 5 0 0 13 27 13 28 8 31 7 26
Debarking 35 24 2 12 3 14 15 75 6 21 4 6 12 26 4 15 3 12
Climate change 23 16 3 18 4 19 3 15 2 7 20 31 15 32 5 19 2 8
Deforestation 19 13 1 6 3 14 3 15 2 7 15 23 5 11 9 35 7 27
Farming 7 5 2 12 5 24 3 15 1 4 17 27 4 9 10 38 7 27
Lack of regeneration 9 6 0 0 0 0 1 5 2 7 7 11 4 9 0 0 0 0
Settle of infrastructures 8 6 0 0 1 5 3 15 0 0 12 19 2 4 1 4 1 4
Overgrazing 6 4 1 6 0 0 0 0 0 0 15 23 3 6 1 4 0 0
Others 3 2 1 6 0 0 0 0 3 11 5 8 2 4 0 0 0 0
Failure of C. toka 4 3 1 6 3 14 0 0 0 0 1 2 0 0 0 0 0 0
ΣF 211 - 21 - 36 - 43 - 21 - 173 - 100 - 44 - 42 -
Potential solutions to the threats Tree/crop association 9 6 3 18 1 5 1 5 0 0 2 3 2 0 2 8 0 0
Planting 38 26 4 24 9 43 4 20 5 18 36 56 2 49 19 73 11 42
Conservation of C. toka and its habitat 47 32 3 18 1 5 0 0 5 18 8 13 28 58 16 62 5 19
Sustainable use of C. toka 22 15 3 18 1 5 0 0 3 11 7 11 4 9 2 8 1 4
Promoting education, and awareness about C. toka 13 9 1 6 0 0 1 5 1 4 11 17 36 2 1 4 1 4
ΣF 129 - 14 - 12 - 6 - 14 - 64 - 72 - 40 - 18 -
Figure 6.

Local perception of the current state of the multiuse species C. toka in Burkina Faso.

The GLM analysis revealed that local knowledge of C. toka’s status varied greatly across ethnolinguistic groups in terms of extinction and stable status, across sexes for all status levels, and across ages for all status levels except decreasing status (p–value < 0.05). Adults and elderly people in the BCZ had dissimilar perceptions of the declining, scarcity, and extinction aspects of C. toka (p–value < 0.05) (see Table 5).

Table 5.

Impact of socio-demographical factors and climatic zones on the current state of C. toka through GLMs analyses.

CZ Variables n Extinct Rare Increasing Decreasing Stable
Ethnolinguistic groups
S Bobo 145 0 ± 0 0.014 ± 0.12 0.23 ± 0.42 0.47 ± 0.5 0.26 ± 0.44
Bozo 17 0 ± 0 0.035 ± 0.22 0.47 ± 2.75 0.92 ± 5.63 0.48 ± 3.08
Dioula 21 0 ± 0 0.048 ± 0.22 0.51 ± 0.51 1 ± 0.51 0.53 ± 0.22
Others 20 0 ± 0 0 ± 0 0.3 ± 0.47 0.45 ± 0.51 0.25 ± 0.44
SS Bobo 28 0.037 ± 0.19 0.074 ± 0.26 0.088 ± 0.27 0.56 ± 0.50 0.30 ± 0.47
Bwaba 64 0.20 ± 0.41 0.42 ± 0.50 0.047 ± 0.21 0.47 ± 0.50 0.078 ± 0.27
Dafing 47 0.043 ± 0.20 0.043 ± 0.20 0.064 ± 0.25 0.79 ± 0.41 0.11 ± 0.31
Mossi 26 0.267 ± 0.46 0.133 ± 0.35 0.067 ± 0.26 0.67 ±0.49 1.333 ± 0.35
Others 26 0.207 ± 0.46 0.103 ± 0.25 0.067 ± 0.26 0.57 ±0.39 1.303 ± 0.32
X2 7.83 2.1 1.15 2.98 6.08
P value 0.00468 0.138 0.295 0.0804 0.02
Sexes
S Female 91 0 ± 0 0.011 ± 0.11 0.269 ± 0.44 0.314 ± 0.47 0.337 ± 0.47
Male 112 0 ± 0 0.027 ± 0.16 0.230 ± 0.42 0.566 ± 0.50 0.168 ± 0.38
SS Female 55 0.15 ± 0.36 0.1 ± 0.30 0.025 ± 0.16 0.7 ± 0.46 0.175 ± 0.38
Male 147 0.123 ± 0.33 0.254 ± 0.44 0.078 ± 0.27 0.561 ± 0.50 0.114 ± 0.32
X2 23.406 39.03 15.41 4.67 10.64
P value 0.00028 < 0.0000 0.00022 0.0309 0.00169
Age
S Old 108 0 ± 0 0.020 ± 0.14 0.215 ± 041 0.479 ± 0.50 0.243 ± 0.43
Adult 95 0 ± 0 0.017 ± 0.13 0.322 ± 0.47 0.406 ± 0.50 0.237 ± 0.43
SS Old 83 0.086 ± 0.28 0.272 ± 0.45 0.074 ± 0.26 0.530 ± 0.50 0.123 ± 0.33
Adult 119 0.178 ± 0.39 0.151 ± 0.36 0.055 ± 0.23 0.671 ± 0.47 0.137 ± 0.35
X2 14.49 34.65 18.26 2.04 4.66
P value 0.00055 < 0.00000 < 0.000 0.153 0.03407

Local perception of the threat factors of C. toka in Burkina Faso

According to the respondents, the sustainability of C. toka is threatened by some unfavourable factors, such as anthropogenic and natural factors. However, 4% of respondents indicated that there are no threats to the sustainability of C. toka. Globally, the threat features to C. toka were perceived as pruning (25%) for food and fodder, climate change (14%), deforestation (10%), ageing (10%), debarking (9%), agricultural expansion (7%), bushfires (6%), and “other” (6%) (Fig. 7). The “other” category referred to the specific habitat of the species, infertility of soil, production of charcoal, diseases, attacks by parasites, fungi, epiphytes, termites, and invasion of Azadirachta indica and Ficus. In the SCZ, the main causes were pruning (21%), deforestation (13%), climate change (13%), debarking (12%), bushfire (9%), ageing (8%) and agriculture (8%) (Fig. 7). Pruning (FL:47%), climate change (FL:18%), debarking (FL:12%), and ageing (FL:12%) were emphasized by the Bozo, and debarking (FL:75%) was emphasized by others in the SCZ (Table 4). In the SSCZ, pruning (28%) and climate change (15%) were reported as the key drivers (Fig. 7). Pruning (FL: 70%), climate change (FL: 32%), ageing (FL: 28%) and debarking (FL: 26%) were reported at a heightened level by the Dafing culture in the SSCZ (Table 4). These disturbances affect the survival of the critically endangered species C. toka.

Figure 7.

Threat factors by climate zone in Burkina Faso. F. of C. toka: failure of C. toka.

The results globally suggested that pruning, climate change, deforestation, ageing, debarking, farming expansion and bushfires are the major factors that threaten the survival of C. toka in the study areas. Pruning, climate change, and deforestation ranked first, second and third, respectively, signifying that they are the most proximate threatening factors (Fig. 7). In the SCZ, ageing was perceived by Bobo culture; climate change by Bozo culture; debarking, pruning, farming and failure of C. toka by Dioula culture; and deforestation and settlement of infrastructures were mentioned by other ethnolinguistic groups as the main predictors of the decline of the species. However, in the SSCZ, deforestation, farming and pruning were the main causes of the extinction of C. toka identified by the Mossi. The Dafing culture believed that C. toka is threatened due to climate change and human activities (bushfires). According to the Bwaba culture, overgrazing and debarking are the key reasons for the threat in the study area (Table 6). In the BCZ, older people emphasized that the species has declined due to climate change, farming, ageing, deforestation, settlement of infrastructure, bushfires, failure of C. toka, pruning and other causes (Table 6). The overall threat factors of C. toka varied only across ethnolinguistic groups for ageing, pruning, climate change, farming, settlement of infrastructure, and lack of regeneration (p–value < 0.05). In addition, the threat drivers were statistically similar (p–value > 0.05) between both sexes and generations for identifying deforestation, settlement of infrastructures, lack of regeneration, failure of C. toka and bushfire as causes (Table 6).

Table 6.

Mean values (± Std) and results of GLM factors considered threats to C. toka in Burkina Faso.

CZ Variables n Climate change Farming Deforestation Settle of infrastructures Ageing Bushfire Overgrazing Lack of regeneration Failure of C. toka Debarking Pruning Others
Ethnolinguistic groups
S Bobo 145 0.131 ± 0.34 0. 048 ± 0.22 0.131 ± 0.34 0.055 ± 0.23 0.172 ± 0.38 0.137 ± 0.35 0.041 ± 0.20 0.062 ± 0.24 0.028 ± 0.16 0.180 ± 0.74 0.329 ± 0.47 0.062 ± 0.24
Bozo 17 0.222 ± 0.43 0.111 ± 0.32 0.056 ± 0.24 0 ± 0 0.111 ± 0.32 0 ± 0 0.056 ± 0.24 0 ± 0 0.056 ± 0.24 0.222 ± 0.43 0.222 ± 0.43 0 ± 0
Dioula 21 0.190 ± 0.40 0.238 ± 0.44 0.143 ± 0.36 0.048 ± 0.22 0.095 ± 0.30 0.095 ± 0.3 0 ± 0 0 ± 0 0.143 ± 0.36 0.381 ± 1.53 0.381 ± 1.53 0 ± 0
Others 20 0.142 ± 0.36 0.190 ± 0.40 0.190 ± 0.40 0.190 ± 0.40 0.048 ±0.22 0.095 ± 0.30 0 ± 0 0.095 ± 0.30 0 ± 0 0.333 ± 0.97 0.367 ± 0.98 0.048 ± 0.22
SS Bobo 28 0.071 ± 0.26 0.036 ± 0.19 0.071 ± 0.26 0 ± 0 0 ± 0 0.036 ± 0.19 0 ± 0 0.071 ± 0.26 0 ± 0 0.038 ± 0.19 0.077 ± 0.29 0 ± 0
Bwaba 64 0.219 ± 0.42 0.265 ± 0.45 0.234 ± 0.43 0.188 ± 0.39 0.359 ± 0.48 0.031 ± 0.18 0.234 ± 0.43 0.109 ± 0.31 0.016 ± 0.13 0.188 ± 1.11 0.234 ± 0.43 0 ± 0
Dafing 47 0.319 ± 0.47 0.085 ± 0.28 0.106 ± 0.31 0.043 ± 0.20 0.276 ± 0.45 0.148 ± 0.36 0.063 ± 0.25 0.085 ± 0.28 0 ± 0 0.26 ± 1.29 0.106 ± 0.31 0.043 ± 0.20
Mossi 26 0.133 ± 0.35 0.267 ± 0.46 0.267 ± 0.45 0.067 ± 0.25 0.467 ± 0.52 0 ± 0 0 ± 0 0 ± 0 0 ± 0 0.2 ± 0.56 0.267 ± 0.45 0 ± 0
Others 26 0.133 ± 0.35 0.267 ± 0.46 0.237 ± 0.41 0.056 ± 0.21 0.237 ± 0.24 0 ± 0 0 ± 0 0 ± 0 0 ± 0 0.2 ± 0.56 0.241 ± 0.36 0 ± 0
X2 6.41 17.7 2.39 3.7 7.03 2.14 0.44 0.896 0.37 1.15 7.65 1.06
P value 0.00986 <0.000 0.117 0.0479 0.00699 0.152 0.499 0.01 0.548 0.301 0.00412 0.304
Sexes
S Female 91 0.144 ± 0.35 0.022 ± 0.15 0.067 ± 0.25 0.022 ± 0.15 0.167 ± 0.37 0.044 ± 0.21 0.022 ± 0.15 0.033 ± 0.18 0.044 ± 0.20 0.178 ±0.44 0.158 ± 0.37 0.040 ± 0.17
Male 112 0.147 ± 0.36 0.139 ± 0.35 0.183 ± 0.39 0.095 ± 0.30 0.130 ± 0.34 0.174 ± 0.38 0.043 ± 0.20 0.070 ± 0.26 0.035 ± 0.18 0.252 ± 1.07 0.167 ± 0.39 0 ± 0
SS Female 55 0.175 ± 0.38 0.125 ± 0.33 0.1 ± 0.30 0.025 ± 0.16 0.35 ± 0.48 0.025 ± 0.16 0.025 ± 0.16 0.075 ± 0.27 0 ± 0 0.075 ± 0.35 0.185 ± 0.37 0 ± 0
Male 147 0.228 ± 0.42 0.184 ± 0.39 0.193 ± 0.40 0.123 ± 0.33 0.254 ± 0.44 0.079 ± 0.27 0.149 ± 0.36 0.088 ± 0.28 0.009 ± 0.09 0.219 ± 1.17 0.221 ± 0.40 0.009 ± 0.09
X2 1.64 5.27 2.12 2.53 2.9 0.05 6.67 1.13 2.12 7.52 0.38 1.26
P value 0.195 0.0184 0.139 0.103 0.0844 0.832 0.00707 0.279 0.169 0.0159 0.3056 0.1504
Age
S Old 108 0.164 ± 0.37 0.103 ± 0.30 0.144 ± 0.35 0.068 ± 0.25 0.171 ± 0.37 0.089 ± 0.29 0.006 ± 0.08 0.048 ± 0.21 0.034 ± 0.18 0.171 ± 0.68 0.164 ± 0.37 0.034 ± 0.18
Adult 95 0.101 ± 0.30 0.051 ± 0.22 0.102 ± 0.30 0.051 ± 0.22 0.085 ± 0.28 0.19 ± 0.39 0.102 ± 0.30 0.068 ± 0.25 0.05 ± 0.22 0.340 ± 1.18 0.101 ± 0.30 0.05 ± 0.22
SS Old 83 0.284 ± 0.45 0.148 ± 0.36 0.136 ± 0.34 0.086 ± 0.28 0.309 ± 0.46 0.062 ± 0.24 0.136 ± 0.35 0.111 ± 0.32 0 ± 0 0.222 ± 1.25 0.284 ± 0.45 0.061 ± 0.20
Adult 119 0.137 ± 0.34 0.192 ± 0.40 0.205 ± 0.41 0.110 ± 0.31 0.247 ± 0.43 0.068 ± 0.25 0.096 ± 0.30 0.055 ± 0.23 0.014 ± 0.117 0.137 ± 0.69 0.137 ± 0.34 0.014 ± 0.117
X2 3.89 0.77 0 0.14 4.2 1.71 1.4 0.95 1.71 0.17 4.51 2.65
P value 0.0445 0.373 0.938 0.699 0.0372 0.2 0.227 0.321 0.215 0.681 0.0299 0.027

Based on our observations in the field, the threat factor in the BCZ could be natural (hole, wind, drought, crown gall, fungi, and epiphyte) as well as anthropogenic. However, old C. toka trees contained very large hollows (Fig. 8) which weakens the species during wind (Fig. 9), or fire action (Fig. 10).

Figure 8.

Risk factor: hollow in most of C. toka natural stands in the BZC. Pictures: Z. Dabré, 2020.

Figure 9.

Risk factor: The effect of wind on C. toka in BCZ. Pictures: Z. Dabré, 2021.

Figure 10.

Risk factor: ageing and fire effect on hollowed out C. toka in SCZ. Pictures: Z. Dabré, 2021.

In addition to the hole, C. toka has a fasciculate root (Fig. 11) which accentuates the effect of wind. Ficus thonningii Blume (Fig. 12), fungi (Fig. 13), and crown gall and holes (Fig. 14) infest C. toka tree species.

Figure 11.

Risk factor: ageing, action of the wind and Azadirachta indica A. Juss. invasion in SCZ. Pictures: Z. Dabré, 2021.

Figure 12.

Risk factor: attack by Ficus thonningii on C. toka species in SCZ. Pictures: Z. Dabré, 2021.

Figure 13.

Risk factor: attack of fungi on C. toka. Pictures: Z. Dabré, 2021.

Figure 14.

Risk factor: holes (yellow round), ageing, crown gall (red round) attacks coupled with debarking in the BCZ. Pictures: Z. Dabré, 2022.

In the study areas, some livelihoods result in the overharvesting of the leaves of this species either for food or fodder uses (Fig. 15), and the bark by traditional healers (Fig. 16). Furthermore, some individuals died, probably due to drought, ageing, or diseases (Fig. 17).

Figure 15.

Risk factor: heavy pruning of C. toka’s leaves in BCZ. Pictures: Z. Dabré, 2021.

Figure 16.

Risk factor: debarking for traditional medicinal purposes in the BCZ. Pictures: Z. Dabré, 2020.

Figure 17.

Risk factor: natural death due either to drought, diseases, or ageing of the hollowed out C. toka in the BCZ. Pictures: Z. Dabré, 2022.

According to our field observations, the assessment of the threat by climatic zones showed that the SCZ was more exposed than the SSCZ (even though C. toka is less abundant in the SSCZ) due to anthropogenic activities such as artisanal activities (Fig. 18), and industrial mining (Fig. 19),and bushfire (see Fig. 10 above).

Figure 18.

Risk factor: Artisanal mining under C. toka tree in the SCZ. Pictures: Z. Dabré, 2021.

Figure 19.

Risk factor: industrial mining in the habitat of C. toka in the SCZ. Pictures: Z. Dabré, 2021.

However, the exploitation of granite negatively affects seed germination and sometimes sapling growth. Some local people often cut C. toka (Fig. 20) for charcoal, firewood, or farm settlement purposes.

Figure 20.

Risk factor: cutting of C. toka sapling in the SCZ. Pictures: Z. Dabré, 2020.

Epiphyte (Fig. 21), grazing by goats and cattle (Fig. 22), and biological invasion by Azadirachta indica A. Juss. (see Figs 11, 21, 22 above) of C. toka organs or saplings were noticed in some livelihoods of the study areas. Epiphytes (Fig. 21) infested C. toka trees to the point that they lost their leaves and remained apparently dead.

Figure 21.

Risk factor: ageing, epiphytic attack (red circles), holes, crown gall (yellow circles), and Azadirachta indica A. Juss. invasion in SSCZ. Pictures: Z. Dabré, 2022.

Figure 22.

Risk factor: ageing, rotting, Azadirachta indica A. Juss. invasion and animal grazing in the SSCZ. Pictures: Z. Dabré, 2022.

Traditional potential solutions to the threat

The conservation strategies proposed by the locals included the conservation of C. toka and its habitat, the sustainable use of C. toka, and the promotion of education and awareness about C. toka. However, planting was the most important solution expressed by all ethnolinguistic groups, as confirmed by the high FL (SCZ: 43%, SSCZ: 73%) value in the BCZ (Table 3). Planting (45%), conservation of C. toka and its habitat (27%), sustainable use of C. toka (14%), promoting education and awareness about C. toka (10%), and tree/crop association (5%) were the future potential solutions proposed to solve the threat posed to C. toka in the study areas. Moreover, potential solutions in the SCZ were planting (34%), conservation of C. toka and its habitat (33%) to protect it from human pressures such as cutting, fire, animal grazing and sustainable use of the species (16%) by avoiding overharvesting (pruning, debarking, and overusing the roots). In the SSCZ, planting (58%), conservation (19%), and sustainable use (10%) were the key solutions proposed to address the threats posed to the species (Fig. 23).

Figure 23.

Traditional potential solutions to the threat according to climatic zones in Burkina Faso.

In the Sudanian climatic zone, conservation, sustainable use of the species, and planting were cited by the Bobo, Bozo, and Dioula cultures, respectively, as potential solutions to the threats posed to the species. According to the Sudano-Sahelian climatic zone, the conservation of the species and its habitat was mostly perceived by the Dafing and planting by the Bwaba as key solutions to address the threat. Most of the solutions were proposed by males in the BCZ. In the SCZ, older people proposed more solutions than younger adults. A contradiction was found in the SSCZ (Table 8).

The chi-square test results of the different responses of informants who were involved in answering whether to plant C. toka show that there is a significant relationship among the respondents in the study sites (Table 7).

Table 7.

Chi-square test showing whether to plant or not C. toka in Burkina Faso.

Climatic zones % of respondents Chi-square
Yes No DF X2 P value
Sudanian 77.02 23.91 1 27.94 < 0.0001
Sudano-Sahelian 99.61 0.39 1 98.43 < 0.0001

The GLM analyses of respondents’ perceptions of potential solutions to the threat posed to C. toka revealed that local perception varied significantly according to ethnolinguistic groups, sex, and ages for the solution of planting and ethnolinguistic groups for the solution of conservation of C. toka and its habitat (p–value < 0.05, Table 8). However, no differences in promoting education and awareness about C. toka, associating C. toka with crops, and sustainable use of the species were found among all the sociodemographic parameters (p–value > 0.05, Table 8).

Table 8.

Mean values (± Std) and results of GLMs of potential solutions to the existence of C. toka in Burkina Faso.

Variables n Planting Conservationof C. toka and its habitat Promoting education, and awareness about C. toka Tree/crop association Sustainable use of C. toka
Ethnolinguistic groups
S Bobo 145 0.262 ± 0.44 0.152 ± 0.36 0.090 ± 0.29 0.062 ± 0.24 0.014 ± 0.11
Bozo 17 0.235 ± 0.44 0.118 ± 0.33 0.059 ± 0.24 0.176 ± 0.39 0.059 ± 0.24
Dioula 21 0.429 ± 0.51 0.048 ± 0.22 0 ± 0 0.048 ± 0.22 0 ± 0
Others 20 0.2 ± 0.41 0 ± 0 0.05 ± 0.22 0.05 ± 0.22 0. 05 ± 0.22
SS Bobo 28 0.179 ±0.39 0.107 ± 0.31 0.036 ± 0.19 0 ± 0 0 ± 0
Bwaba 64 0.563 ± 0.5 0.094 ± 0.29 0.172 ± 0.38 0.031 ± 0.18 0.031 ± 0.18
Dafing 47 0.489 ± 0.51 0.064 ± 0.25 0.021 ± 0.15 0 ± 0 0.021 ± 0.15
Mossi 26 0.7 ± 0.51 0 ± 0 0.087 ± 0.26 0 ± 0 0 ± 0
Others 26 0.6 ± 0.51 0 ± 0 0.067 ± 0.26 0 ± 0 0 ± 0
X2 19.55 15.56 1.41 4.21 0.48
P value < 0.000 < 0.00 0.244 0.051 0.477
Sexes
S Female 91 0.189 ± 0.39 0.111 ± 0.31 0.033 ± 0.18 0.044 ± 0.21 0.033 ± 0.18
Male 112 0.336 ± 0.47 0.133 ± 0.34 0.106 ± 0.30 0.088 ± 0.29 0.009 ± 0.09
SS Female 55 0.5 ± 0.51 0.1 ± 0.30 0.15 ± 0.36 0.025 ± 0.16 0 ± 0
Male 147 0.464 ± 0.50 0.070 ± 0.26 0.070 ± 0.26 0.009 ± 0.09 0.026 ± 0.16
X2 6.09 0.29 0.29 0.27 0.05
P value 0.013 0.596 0.587 0.613 0.831
Age
S Old 108 0.285 ± 0.45 0.118 ± 0.32 0.056 ± 0.23 0.063 ± 0.24 0.021 ± 0.14
Adult 95 0.24 ± 0.43 0.136 ± 0.35 0.119 ± 0.33 0.087 ± 0.28 0.017 ± 0.13
SS Old 83 0.469 ± 0.50 0.49 ± 0.21 0.135 ± 0.34 0.025 ± 0.16 0.012 ± 0.11
Adult 119 0.479 ± 0.50 0.109 ± 0.31 0.041 ± 0.20 0 ± 0 0.027 ± 0.16
X2 5.53 1.31 0.2 2.24 0.01
P value 0.018 0.260 0.650 0.151 0.913

Discussion

Local perception of the current state of the agroforest tree C. toka in Burkina Faso

The spatial dynamics of C. toka declined in the study area. This could be explained by the fact that the species was once rare. For instance, Gonzalez et al. (2012) emphasized that the density of C. toka has declined in the Guinea ecological zone of the African Sahel due to the climate. Moreover, human action could be the reason for the decrease in C. toka in Burkina Faso. Most youths were unaware of the value of this species; therefore, they cut saplings as well as adult trees. In addition, to establish agricultural land, some residents cut down C. toka individuals. Moreover, habitat loss could be the factor responsible for the changes in the species’ population dynamics. However, the transformation of the species’ habitat (gallery forests) by market gardening or exotic plants could explain its decline. For instance, in the Sudanian climatic zone, the habitat of C. toka was converted into vegetable crops (such as tomatoes, cucumbers, strawberries, eggplants, sorrels, carrots, papaya and others) and exotic tree plantations (Mangifera indica L., Tectona grandis L.f., Anacardium occidentale L., Eucalyptus camaldulensis Dehnh., Annona muricata L., Annona squamosa L., Delonix regia (Boj.) Raf., Citrus lemon (L.) Burm.f.). Dansi et al. (2013) demonstrated that the threat posed to C. toka may be due to forest destruction, bushfires, destructive harvesting methods and a lack of knowledge about the species. In the Sudano-Sahelian zone, C. toka was reported to be rare and even extinct. This extinction could be due to a lack of regeneration to replace the ageing population of the species. Research has shown that the threat posed to C. toka in northern Cameroon is due to the lack of regeneration. For instance, the regeneration was 0% in an unprotected area and 0.14% in protected areas (Moksia et al. 2019). According to the Mossi and other cultures from the SSCZ, the species was extinct due to overexploitation, the change in the environment and the failure of C. toka in the area. Hence, C. toka has extremely small population sizes and therefore is in extreme danger of extinction. For instance, it was difficult to obtain two or three individuals in the same area, and most of them were old and isolated in their communities. Additionally, the use of the species for traditional medicine may have contributed to its extinction in some study sites, mostly in the Sudano-Sahelian communal zone. Climate has a greater impact on the species abundance and distribution in the Sudano-Sahelian climatic zone than in the Sudanian climatic zone because C. toka is denser in the Sudanian than in the Sudano-Sahelian region. Deforestation caused by agricultural development, infrastructure installation, and climatic variability has an impact on the spatial dynamics of C. toka. Similar findings were reported by Hahn-hadjali and Thiombiano (2000); Garzuglia (2006); Vodouhe et al. (2007); Thiombiano et al. (2010); Bayala et al. (2011); Savadogo et al. (2017) in Burkina Faso. Moreover, C. toka is either extinct or endangered in Chad (Tchobsala et al. 2022), rare in Yemen (Al-Khulaidi 2018), and rare and threatened in Saudi Arabia (Alfaifi et al. 2021).

Hence, different ethnolinguistic groups, sexes and generations have diverse views on the status of C. toka due to cultural differences. Traditional knowledge of the dynamics of C. toka is influenced by ethnolinguistic groups over time. The scarcity and decline of C. toka have been perceived by most sociocultural groups. For instance, the declining factor of C. toka was perceived more strongly by the Bobo, Bozo, Dioula Dafing, and Mossi cultures. This is because those cultures are autochthonous and know the status of the species over time. Traditional healers (Bobo, Bwaba, Dioula, Mossi), hunters (Bwaba) and fishermen/women (Bozo) who interact with the habitat of C. toka have a better knowledge of the species’ status. Knowledge of the declining characteristics of C. toka within a hamlet is similar from one generation to another. This could be explained by the fact that both younger adults and the elderly were aware of the species’ status and thus noticed the decline and/or extinction of C. toka.

Threat to the sustainability of the sacred tree C. toka in Burkina Faso

Even though C. toka is a tree associated with mysticism, it faces diverse threats to its continued existence from various anthropogenic activities and natural factors. Extinction and decline of C. toka are due to a range of factors, including overharvesting (pruning, debarking, and rooting), climate change, deforestation, ageing of the population, and farming expansion. According to rural residents, overexploitation is the most serious threat because, in conjunction with the scarcity of C. toka, organs were harvested in an anarchic way. These findings were similar to those of Moksia et al. (2019). Respondents were confident that roots, leaves, and bark are a critical part of C. toka; therefore, its overharvesting may affect its reproduction.

Overharvesting of bark and leaves has been reported to have reduced fruit production in Burkina Faso (Nacoulma et al. 2017). Furthermore, heavy pruning could affect tree development and photosynthesis (Suchocka et al. 2021). Three percent (3%) of the rural community thought C. toka was endangered due to a lack of regeneration. Regeneration could be influenced by either seed availability or seed quality. C. toka has been overpruned to the point where it no longer produces fruits in some areas. The lack of seeds may be the primary cause of the lack of regeneration. Gaoue et al. (2011) demonstrated that the overharvesting of fruits and seeds exposes natural stands vulnerable to population ageing due to the threat to natural regeneration. Overgrazing may also contribute to a lack of regeneration. Four percent (4%) of locals believed that the scarcity of species was caused by overgrazing of seedlings and saplings. Harvesting roots, bark, and even leaves may expose C. toka to diseases such as fungal pathogens, galls, epiphytes, termite attacks, and others. These pathogens could drive the species to extinction by interfering with C. toka reproduction, increasing competition for nutrients, and most likely causing mortality. However, Boussim et al. (2004) indicated that C. toka is parasitized by a pest called Tapinanthus globiferus (A.Rich.) Tiegh. However, Otry and Laflamme (2009) confirmed that various fungi are pathogens of specific tree species and cause tree mortality in vulnerable trees. Approximately 12% of the respondents stressed that climate change is one of the reasons for the extinction of the taboo species. They noticed that during the past 30 years, there have been drastic changes in the frequency and volume of precipitation patterns, rising temperature and wind. Sop and Oldeland (2011) stated that drought is one of the primary causes of vegetation change in the Sub-Sahel of Burkina Faso. However, strong winds in the savannah and rocky zones cause the ageing population of the species to easily be uprooted because the species lacks a taproot, while drought causes the species to dry out. Furthermore, because the ideal temperature for C. toka is between 26 and 30 °C, an increase in temperature could inhibit regeneration (Watrin et al. 2007). According to respondents, floods have an impact on C. toka habitat by destroying habitat and uprooting any C. toka found on the banks because some of them had their roots hanging in the rivers in some way. In addition, ageing (13%) leads to the death of C. toka. Thus, drought and pathogens can hasten this death. Franklin et al. (1987) demonstrated that tree death is a natural ecological process involving one or more pathogens and other microbes. However, the proportion of farming expansion (7%) and urbanization (4%) was less of a contribution to the extinction of the sacred tree C. toka. These factors are still a major challenge today because the human population is growing, and forests are being destroyed to make way for infrastructure and farmlands. According to locals, previously, the C. toka tree was not widespread (1%) in different villages of Burkina Faso, and it was not accessible even for local food, fodder, firewood, and medical purposes. Most of the fishermen, hunters and traditional healers had to travel to other villages to look for the organs of C. toka. According to the respondents, fire (6%) may impact the seeds, seedlings, saplings and even the age population of the species. However, bushfires could reduce the abundance of seedlings by killing seedlings and decreasing the seed bank of C. toka in the soil. Furthermore, bushfires may influence the trunk and hollows of adult individuals, which could potentially lead to the death of the species. Fire triggers plant mortality throughout the crown, stem and root (Miller and Findley 2014). The severity and impacts, at the regional and global scales, of the burned area resulting from wildfires, have increased in recent decades (Doerr and Santin 2016). Wildfires have an impact on soil properties (Agbeshie et al. 2022), making plant species vulnerable to a decline (Miller et al. 2019). Local knowledge of the threat factors of C. toka was dissimilar among the ethnolinguistic groups, generations, and sexes due to the diversity of cultures.

Potential traditional solution to the threat

Three of the five concepts of the Global Strategy for Plant Conservation are the conservation of the species and its habitat, sustainable use, and promotion of education and awareness (CBD 2002). Planting remains the main solution to combat the threat in the BCZ. Although the sacred species C. toka was rare and extinct in some areas, no individuals were found planted near houses, such as in northern Cameroon, where C. toka was planted for agro-silvopastoral purposes (Neba 2009). Additionally, C. toka was planted in farmland in Ethiopia (Rolkier and Abebe 2015). Most rural residents agreed to plant C. toka on their farmlands and in public places (markets, administrations, and schools) because they believed it was the best way to save the species. Some rural residents have decided not to plant it in their compounds because they know that C. toka is a massive plant. Furthermore, the mystical nature of C. toka may have discouraged locals from domesticating it. The second possible solution was the in-situ conservation of C. toka and its habitat (13%) to protect it from all human activities, including animal grazing, bushfires, and cutting of saplings and adult trees. Farmers must respect the 100-metre limit on riverbanks for the conservation of natural habitat. Respondents believed that farming within 100 meters of the riverbanks could cause siltation of water bodies and affect species regeneration. Agricultural activities such as tillage and ploughing cause the siltation of streambeds, resulting in the loss of the original water source (Kumar et al. 2021) and shortening its useful life (Poleto and Beier 2012). However, the conservation of habitats may be the best solution to the threat because seeds could be obtained from the remains of individuals and could be used to produce seedlings in nurseries. Seedlings have the potential to aid in reforestation and soil restoration. For instance, C. toka could be used as a keystone plant to restore deeply destroyed ecosystems. Furthermore, reintroducing C. toka into a restoration framework can aid in the prevention of extinction. The main solution to extinction is in situ and ex-situ conservation of a species (Oldfield 2003). Furthermore, invasive species should be removed from the habitat to reduce competition. According to Barney et al. (2013), invasive alien species alter nutrient pools and fire regimes. However, rural people stated that C. toka is scarcer and more threatened than Vitellaria paradoxa C.F.Gaertn., Lannea microcarpa Engl. & K. Krause, Parkia biglobosa (Jacq.) R. Br. ex G. Don, Bombax costatum Pellegr. & Vuillet, Adansonia digitata L., and yet it is not protected. To reduce the rate of decline of C. toka, local people suggested associating crops with C. toka. We recommend in situ, ex-situ, and circa-situ conservation of C. toka. Circa-situ conservation is a successful conservation strategy in traditional agroforestry systems and backyard gardens (Sanchez et al. 2010; Lokonon et al. 2021). As such, we recommend that local communities increase their capacity to cultivate the species and replant it in traditional agricultural landscapes and home gardens, as well as promote youth education about good practices and harvesting techniques for plant parts used in food, fodder, medicine, or other specific uses.

Conclusion

This study has shown that the local people of the Sudanian and Sudano-Sahelian areas are aware of the ecological status of C. toka, as well as the potential driving factors influencing species dynamics. Celtis toka was described to be in a state of decline and extinction (in the Sudano-Sahelian zone) due to anthropogenic activities combined with climate change, lack of regeneration and species failure. Moreover, efforts should perhaps be concentrated on the domestication of C. toka to enhance regeneration and increase production. Conservation efforts should perhaps focus on C. toka and its habitat. However, most of the local future potential solutions included planting; conservation of the species, its seeds, regeneration, and its habitat; avoidance of the overuse of C. toka; fire protection; association of C. toka in farmland; and promoting education and awareness of youth about C. toka. The incorporation of local people’s perceptions into policymaking is of critical importance in C. toka management and for its sustainable conservation strategies. The findings of this study will aid the conservation of the critically endangered species C. toka at the national level by informing future environmental and biodiversity conservation efforts. Moreover, C. toka could be used to rehabilitate and restore degraded ecosystems to promote the recovery of the species.

Acknowledgements

We gratefully acknowledge the German Federal Ministry of Education and Research (BMBF) and West African Science Centre for Climate Change and Adapted Land Use (WASCAL) for providing the scholarship and financial support. This article is the result of a truly collective effort. First, we express our sincere gratitude to all field guides and translators for providing guidance and linguistic editing in the field. We acknowledge all the interviewees who agreed to share their expertise. We would also like to thank Mrs Alpha Karbgo and Ugbor Ogechi Nnabuchi. Finally, we would like to recognize the anonymous reviewers for their insightful comments on this manuscript.

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