1. Introduction
Community forests are forests collectively managed by local communities to protect biodiversity and support livelihoods. Thy are governed by customary rights, rules, and institutions that pre-date most modern governments, and continue to adapt to changing circumstances. They could have spiritual and cultural connotation (sacred groves and forest) exclusively [
1,
2,
3] or not. They provide non-timber (foods, medicines products, cosmetics, honey, meats…), timber products and others services. Thus, community forests are important for several reasons, as they provide a wide range of social, political, environmental and economic benefits[
4]. They also provide primary source of livelihood, nutrition and employment. They contribute to biodiversity conservation, improve forest restoration and climate resilience [
5,
6,
7,
8].
The protection of biodiversity through sacred and community forests is of growing international concern in Africa and elsewhere [
5,
9,
10,
11,
12,
13]. These are the objectives of the Togolese government. Since 2015, it has produced a guide to community forestry. Several projects supporting community forest initiatives were then launched. Currently, 171 community forests can be found nationwide[
9]. Fewer of these, however, comply with the Guide. Moreover, there is a lack of scientific data to help guide how to manage them. These data include knowledge of biodiversity, landscape structure and dynamics, timber resource status, management practices and the existence and functioning of management committees. Although several studies have investigated about the management of both community forests [
9,
10,
14,
15,
16,
17,
18,
19] and sacred groves and forests [
1,
20,
21], however, there is lack of relevant data on Savannah community forest dynamics. Thus, such knowledge can be helpful in enhancing our understanding of the role of local communities in managing forest resources [
22]. Our study will provide vital information necessary to improve sustainable community forest management practices.
As a result of climate change and the increase in population, the savannah region has had less forest cover. Agroforestry parklands cover most of the land [
23]. Protected areas are sometimes the only forest ecosystems. Unfortunately, these protected areas have undergone significant degradation since the socio-political unrest in the 1990s [
24,
25,
26,
27,
28]. For species that have already disappeared or are threatened with extinction, sacred and community forests thus serve as true sanctuaries.
The present study, carried out on the Kouampante Community Forest (KCF), aims to demonstrate the contribution made by the KCF to restoring forests and conserving biodiversity in Togo. More specifically, it: (i) analysed the dynamics of the forest ecosystem from 2010 to 2020, (ii) assessed the diversity of plant species, and (iii) characterised the demographic structure of woody plants in KCF.
2. Methodology
2.1. Study area
Kouampante Community Forest (KCF) is located in Ogaro Canton, Kpendjal-Ouest Prefecture, Savannahs Region, Togo. The target forest belongs to Togo's ecological zone I [
29]. The native vegetation of the Soudanian savannahs is dominated by thorny species [
30,
31]. Due to the increasing human population, the native ecosystems have been transformed into croplands and agroforestry parklands [
28]. Several agroforestry parklands have been found. The predominant agroforestry trees are raost palms (
Borassus spp), african locust bean (
Parkia biglobosa Jacq), tamarind (
Tamarindus indica L.), African baobab (
Adansonia digitata) [
15,
23,
32,
33,
34]. These agroforestry trees play an important role in improving local nutrition and livelihoods [
35,
36]. In addition to cropland expansion [
23,
28], grazing is highlighted as a second threat to plant communities [
37]. Protected areas of the savannahs region, long known as a technique to conserve biodiversity and ecosystems, are also highly degraded and invaded [
27,
38,
39]. To counter this degradation, community forests and sacred forest/grove practices are seen as an opportunity to conserve biodiversity [
9].
Figure 1.
Location and sampling design within Kouampante Community Forest in Togo.
Figure 1.
Location and sampling design within Kouampante Community Forest in Togo.
2.2. Data Collection
2.2.1. Satelite image acquisition
LocustMap, a mobile application, was first used to delineate the boundaries of the KCF. The KML shapefile was then projected onto Google Earth images supplied by Astrium Service to Google Inc 2010, 2014, 2020 for the digitisation of the land use units. These images were chosen due to their high resolution (up to 1.5 m) and the small area covered by the KCF [
40,
41].
2.2.2. Sampling design
Thirteen sample plots, equidistant by 100 m, were established along three transects separated by 200 m. Four types of inventories were carried out: the phytosociology, the ecology, the forestry and the regeneration. The phytosociology of the woody species, the ecology and the forestry parameters were assessed within plots of 50 m x 20 m in size[
15]. For the phytosociology of herbaceous species, sub-plots of 10 m x 10 m were established in the centre of the main plot[
42]. Within the main plot, 3 subplots of 5 m x 5 m were defined for regeneration inventories, one in the centre and the other two in the opposite corners on both sides of the central plot, arranged diagonally [
42,
43,
44].
2.2.3. Inventories
The phytosociological inventory of plants has been carried out on the basis of the Braun-Blanquet (1932) abundance/dominance scale. This scale is defined as follows: rare species, coverage 0-1% (+); coverage 1-5% (1); coverage 5-25% (2); coverage 25-50% (3); coverage 50-75% (4); coverage 75- 100% (5). Vegetation type, grazing, wildfire, erosion were recorded as ecological parameters. Tree diameter, stem height and total height of woody plants with DBH ≥ 5 cm were measured during the forest inventory[
45]. A forestry compass was used to measure tree diameter at 1.30 m above the ground. Stem height and total height were assessed by visual evaluation. All woody species with DBH < 5 cm [
33] were defined as potential regeneration.
2.3. Data Analysis
2.3.1. Land Use Unit Mapping
The different land-use units of KCF were digitised using Google Earth Pro software. To validate the digitised occupation units, ground truth points were projected. The resulting shapefiles were transferred to QGIS 2.30 for mapping [
40]. WGS 84_UTM Zone 31N was used as the projection background. Land use dynamics and transition were determined by comparison of the different maps[
46].
2.3.2. Assessment Of The Floristic Diversity
The vegetation data collection was downloaded in Microsoft Excel spreadsheet format. A list of the plants of the Kouampante forest were then drawn up. The genera and botanical families were used to classify each species listed. Classification used was APG IV[
10], which was accessed from the website:
https://africanplantdatabase.ch/en. Biotypes and chorology were established [
47,
48]. The following biotypes were considered: phanerophytes (Ph), chamephytes (Ch), hemicryptophytes (He), geophytes (Ge), therophytes (Th) and epiphytes (Ep). Phanerophytes include: megaphanerophytes (MP) (trees over 30 m), mesophanerophytes (mP) (trees 10 to 30 m), microphanerophytes (mp, trees 2 to 10 m), nanophanerophytes (np, trees 0.4 to 2m), lianaceous forms (Lnp, Lmp, LmP, LMP) [
25]. A tropical African context was used for the chorology. These are as follows: GC = species known in Guineo-Congolese zone, GCW = species belonging to western forest massif, GCE = species belonging to eastern forest massif, SZ = species known in Sudano-Zambesian zone, GC-SZ = species found in both zones, I = species introduced for agriculture, forestry or horticulture.
2.3.3. Forest Characteriscics Analysis
Four major dendrometric parameters were evaluated: tree density per hectare (D), mean lorry height (HL in m), mean diameter (Dm in cm) and basal area (G in m2/ha) [
16,
33]. Trees with DBH ≥ 5 cm were considered. Mean Lorey Height is calculated by averaging tree heights weighted by basal area [
49]. Trees are classified into diameter and height classes. The minimum diameter is 5 cm and the minimum height is 2 m. To fit the demographic structure of the trees to the theoretical distribution, the 3 Weibull parameters (a = location parameter, b = scale or size parameter and c = shape parameter related to the diameter or height structure) were used[
33].
3. Results
3.1. Land Use Units Dynamic
An analysis of Google Earth images shows that the Kouampante community forest in 2010, 2014 and 2020 consists of tree savannah/shrub savannah and arable/fallow land (
Figure 2). The same occupations were represented in 2014. Tree/shrub savannahs accounted for 33% of the forest. Croplands/Fallows accounted for 67%. In 2010, tree savannah/shrub savannah covered 58.73% of the forest, followed by cropland and fallow (41.27%). In 2020, tree savannahs/shrub savannahs occupy 84.30% of the Kouampante CF. This is followed by croplands/ fallow land (15.70%).
Between 2010 and 2020, the Kouampante community forest was characterised by a decrease in croplands/fallows (-61.97%). This contrasts with an increase in tree/shrub savannah (43.55%) (
Table 1).
By analyzing the land use transition matrix for the Kouampante community forest (
Table 2), it was possible to identify the main conversions between 2010 and 2020. A conversion rate of 4.23% was applied to the conversion of trees/shrub savannahs to croplands/fallows. Stability exists for 11.06% croplands/fallows and 53.04% tree/shrub savannahs (
Figure 3).
3.2. Floristic Diversity of Kouampante Community Forest (KCF)
A total of 59 species from 50 genera and 24 families were recorded.
Detarium microcarpum Guill. & Perr. is the dominant and frequent species in the whole landscape. Occupying 37.73%, this species was recorded in all plots. Guiera senegalensis J.F.Gmel. is the second most abundant species (11,39 %). Apart from
D. microcarpum, the most frequent species are:
Vitellaria paradoxa C.F.Gaertner subsp.
paradoxa and
Combretum collinum Fresen (
Figure 4).
Fabaceae is the most diverse and abundant of the families. It accounts for 48.68% and is made up of 14 plant species. Combretaceae follows with 6 species (19.41%). Rubiaceae and Poaceae each have 6 species and Malvaceae has 4 species. The other families are less diverse (
Figure 5).
In the KCF, tree phytogeographical plant species are represented. Soudano-Zambezian species (SZ, 54.24%) were the most common. They were followed by the transitional species (GC-SZ: Guinea-Congolese/Soudano-Zambezian 42.37%). Introduced species were the least represented (I: 3.39%).
The most represented biotypes in the KCF are microphanerophytes and nanophanerophytes (
Figure 6). The less diverse and abundant species are the chamephytes and the geophytes.
One endangered species (Vitellaria paradoxa) and one near-threatened species (Terminalia laxifolia Engl.) were included in the KCF floras. IUCN Red List criteria are not applicable to 38.98%. A proportion of 61.02% of the plants are of least concern.
3.3. Descriptrion of woody plant communities
There were 16 species in the woody plant community of KCF.
Detarium microcarpum was the most important species (IVIsp = 128.68%). This key species is followed by
Vitellaria paradoxa (
Table 3). The 16 woody species are divided into genera and 7 families. The Fabaceae family is the most diverse family with 6 species (
Table 3). It is also the most dominant and densest family. As a result, it is so far the most important of the KCF (FIV = 168.54%). Average density was estimated at 99 stems/ha. Mean diameter and basal area were 18.11 cm and 2.53 m²/ha respectively. Mean height was 7.57 m.
3.4. Demographic structure
There is an inverted J-shape (with c<1) in the distribution of trees by diameter and height classes. The most dominant trees are those with small diameter and height. More than half of the trees are between 5 and 10 m in diameter and between 2 and 4 m in height. They account for 59.69% and 58.14%, respectively.
Figure 7.
Kouampante Community Forest woody plant diameter and height structure.
Figure 7.
Kouampante Community Forest woody plant diameter and height structure.
4. Discussion
Between 2010 and 2020, the analysis of Google Earth images of the Kouampante community forest shows a progressive vegetation dynamic. A regression of croplants/fallows to tree/shrub savannahs was observed. This result is comparable to that found in Alibi 1 community forest [
50] and in the Aboudjokopé forest [
40] in the Central Region and the Plateaus Region of Togo respectively. These studies highlighted the contribution of community forest in forest restoration. The progression of tree/shrub savannah in 2020 is due to the protective measures implemented by the community. This could be due to the lasting management of these forest by local communities following reforestation[
15]. Protection against wildfire, plantation of several plants, regulation of human activities and promotion of socioeconomic activities in and around community forests recently by the means of several projects could justify this state [
9,
51]. With the exception of the Abdoulaye wildlife reserve [
43], all protected areas of Togo experience anthropogenic pressure conducing to regression of forest lands [
38,
42,
52,
53]. The same trends were described in West African protected areas [
54,
55].
KCF has an estimated flora diversity of 59. Compared to most other community forests in ecological zones 3, 4 and 5 of Togo [
10,
18,
19,
41,
56], this diversity was low. The smaller size of this forest and the climatic conditions of the area may explain this difference. The low rainfall limited the diversity. KCF plant species diversity was comparable to that of Dankpen district [
15] with a similar climatic conditions.
Globally, the most common families are Fabaceae and Combretaceae. The climatic conditions and vegetation type of the area are confirmed by this finding. Native vegetation was Sudanese savannah with Fabaceae (sometimes thorny
Acacia) and Combretaceae[
30,
31]. This finding was comparable to that of the sacred groves of the Savannahs Region[
20]. In contrast, within the complex of protected areas of Oti-Kéran-Mandouri, located in the same ecological zone, the study of Polo Akpisso
et al. (2015) showed that the Poaceae were the most represented. This showed that KCF had more woody vegetation. However, the structural characteristics of the woody vegetation showed that there were more young trees in the KCF. Meliaceae (represented mainly by
Azadirachta indica, an introduced and invasive species), recently described as dominant in ecological zone 1 [
45,
57] was not present in NCF.
High woody plant abundance was confirmed by high representation of phanerophytic plant species. This was an indication of the reduction of anthropogenic threats in comparison with the protected areas of the zone, which are under high human pressure [
27,
42]. Therefore, managing this vegetation in a sustainable way may result in having open forests.
As a feature of the area, the KCF is dominated by Soudano-Zambezian species. This is comparabl e to several studies in Ecological Zone 1 [
42,
45,
58]. The transitional species were the most abundant in the sacred groves of Savannahs Region and the classified forest of Doungh Pit[
20,
27]. This showed that the KCF was less humid than the latter two.
Inverted J-shape diametric and height distribution observed in KCF. This suggests a high presence of young individuals in the KCF. It also underlines the recent forest protection measures. This is a consequence of the absence of large diameter trees[
27]. It also suggests the presence of several future stems to ensure that the forest continues to recover [
59]. This condition has been described in several community forests in Togo [
14,
16,
41,
56]
5. Conclusion
Improving ecosystem functionality of community-managed forests is crucial for preserving biodiversity. The present investigation described qualitative vegetation characteristics in Kouampante Community Forest. The spatio-temporal dynamics indicate forest recovery within the Kouampante Community Forest. The originality of the climatic conditions of Ecological Zone 1 was demonstrated by the diversity of the KCF. The most dominant plants are woody species with small diameters and heights. This highlighted the recent measures taken to protect the previously anthropogenic threatened area. It represents an opportunity for restoring the forest. The forest must be enriched with useful and nationally threatened species. Special attention should be paid to fire management, as the ecosystems in the area are vulnerable to forest fires. The study details the ecological characteristics of Kouampante Community Forest in Togo. The findings can serve as a basis for the sustainable use and conservation of community-managed forests in the region.
Funding
“This research was funded by the German Federal Ministry of Education and Research (BMBF), through the West Africa Science Service Center on Climate change and Adapted Land Use (WASCAL) program”.
Data Availability Statement
WASCAL data is open access and will be made available when a formal request is received by the institution through the Data Administration Unit.
Acknowledgments
The authors are grateful to the German Federal Ministry of Education and Research (BMBF) for funding this study under the West African Science Service Centre on Climate Change and Adapted Land Use (WASCAL) program. We are grateful to all the stakeholders who invested their time and shared their experiences, and to the anonymous reviewers for their careful reading and comments on this manuscript.
Conflicts of Interest
“The authors declare no conflicts of interest.”
Appendix A. List of plant species within Kouampante Community Forest (NCF)
Annexe 1.
List of plant species within Kouampante Community Forest (KCF) in Togo.
Annexe 1.
List of plant species within Kouampante Community Forest (KCF) in Togo.
Species |
Families |
TP |
TB |
Acacia amythethophylla Steud. ex A. Rich. |
Fabaceae |
SZ |
mP |
Acacia dudgeonii Craib ex Holland |
Fabaceae |
SZ |
mp |
Acacia gourmaensis A.Chev. |
Fabaceae |
SZ |
mp |
Andropogon tectorum Schumach. & Thonn. |
Poaceae |
GC-SZ |
H |
Annona senegalensis Pers. |
Anonanceaae |
GC-SZ |
np |
Bombax costatum Pellegr. & Vuillet |
Malvaceae |
SZ |
mP |
Borassus aethiopum Mart. |
Arecaceae |
GC-SZ |
mP |
Bridelia scleroneura Müll.Arg. |
Phyllanthaceae |
SZ |
np |
Burkea africana Hook. |
Fabaceae |
SZ |
mp |
Cleome monophylla L. |
Cleomaceae |
GC-SZ |
Th |
Cochlospermum planchonii Hook.f. |
Bixaceae |
SZ |
np |
Cochlospermum tinctorium A.Rich. |
Bixaceae |
SZ |
np |
Combretum adenogonium Steud. ex A.Rich. |
Combretaceae |
SZ |
mp |
Combretum collinum Fresen. |
Combretaceae |
SZ |
mp |
Combretum nigricans Lepr. ex var. elliotii (Engl. & Diels) Aubrev. |
Combretaceae |
GC-SZ |
mP |
Crossopteryx febrifuga (G.Don) Benth. |
Rubiaceae |
GC-SZ |
mp |
Dactyloctenium aegyptium (L.) WilId., |
Poaceae |
GC-SZ |
H |
Desmodium gangeticum (L.) nc. var. gangeticum
|
Fabaceae |
GC-SZ |
np |
Detarium microcarpum Guill. & Perr. |
Fabaceae |
SZ |
mp |
Dioscorea rotundata Poir. |
Dioscoreaceae |
GC-SZ |
G |
Eleusine indica (L.) Gaertn. |
Poaceae |
GC-SZ |
H |
Entada abyssinica Steud. ex A.Rich. |
Fabaceae |
GC-SZ |
Lmp |
Euphorbia convolvuloides Hochst. ex Benth. |
Euphorbiaceae |
SZ |
Ch |
Feretia apodanthera Delile ssp. apodanthera
|
Rubiaceae |
SZ |
mp |
Ficus ingens (Miq.) Miq. |
Moraceae |
SZ |
mp |
Gardenia aqualla Stapf & Huteh. |
Rubiaceae |
GC-SZ |
np |
Gardenia erubescens Stapf & Huteh. |
Rubiaceae |
GC-SZ |
np |
Grewia lasiodiscus K. Schum. |
Malvaceae |
SZ |
mp |
Grewia cissoides Hutch. & DalzieI |
Malvaceae |
SZ |
mp |
Guiera senegalensis J.F.Gmel. |
Combretaceae |
SZ |
np |
Gymnosporia senegalensis (Lam.) Loes. |
Celastraceae |
SZ |
np |
Hyptis spicigera Lam. |
Lamiaceae |
SZ |
np |
Hyptis suaveolens (L.) Poit. |
Lamiaceae |
GC-SZ |
np |
Lannea acida A.Rich. s.l. |
Anacardiaceae |
GC-SZ |
mP |
Loudetia hordeiformis (Stapf) C.E.Hubbard |
Poaceae |
GC-SZ |
Th |
Ozoroa insignis Delile |
Anacardiaceae |
SZ |
np |
Parinari curatellifolia Planch. ex Benth. |
Chrysobalanaceae |
SZ |
mp |
Parkia biglobosa (Jacq.) R.Br. ex Benth. |
Fabaceae |
GC-SZ |
mP |
Pennisetum polystachion (L.) Sehult. polystachion
|
Poaceae |
GC-SZ |
Th |
Piliostigma thonningii (Schumach.) Milne-Redh. |
Fabaceae |
GC-SZ |
np |
Prosopis africana (GuilI. & Perr.) Taub. |
Fabaceae |
SZ |
mP |
Pteleopsis suberosa Engl. & Diels |
Combretaceae |
SZ |
mp |
Sarcocephalus latifolius (Sm.) E.A.Bruce |
Rubiaceae |
GC-SZ |
Lmp |
Securidaca longepedunculata Fresen. |
Polygalaceae |
SZ |
mp |
Senna obtusifolia (L.) H.S.Irwin & Barneby |
Fabaceae |
GC-SZ |
np |
Spermacoce radiata (DC.) Hiem |
Rubiaceae |
GC-SZ |
Th |
Sterculia setigera Delile |
Malvaceae |
SZ |
mP |
Stereospermum kunthianum Cham. |
Bignoniaceae |
SZ |
mP |
Strychnos spinosa Lam. |
Loganiaceae |
SZ |
mP |
Tamarindus indica L. |
Fabaceae |
GC-SZ |
mP |
Tectona grandis L.f. |
Verbenaceae |
I |
mP |
Tephrosiaflexuosa G.Don |
Fabaceae |
GC-SZ |
Th |
Terminalia laxifolia Engl. |
Combretaceae |
SZ |
mp |
Thelepogon elegans Roth ex Roem. |
Poaceae |
SZ |
Th |
Vigna subterranea (L.) Verde. |
Fabaceae |
I |
Th |
Vitellaria paradoxa C.F.Gaertner subsp. i |
Sapotaceae |
SZ |
mP |
Vitex simplicifolia Oliv. |
Verbenaceae |
SZ |
np |
Ximenia americana L. |
Olacaceae |
GC-SZ |
mp |
Ziziphus mucronata Willd. |
Rhamnaceae |
SZ |
mp |
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