International Journal of Forestry Research
Volume 2016 (2016), Article ID 7593681, 12 pages
http://dx.doi.org/10.1155/2016/7593681

Research Article

Tree Species Diversity, Richness, and Similarity in Intact and Degraded Forest in the Tropical Rainforest of the Congo Basin: Case of the Forest of Likouala in the Republic of Congo

Suspense Averti Ifo,¹ Jean-Marie Moutsambote,² Félix Koubouana,² Joseph Yoka,³ Saint Fédriche Ndzai,² Leslie Nucia Orcellie Bouetou-Kadilamio,³ Helischa Mampouya,² Charlotte Jourdain,⁴ Yannick Bocko,³ Alima Brigitte Mantota,² Mackline Mbemba,² Dulsaint Mouanga-Sokath,² Roland Odende,² Lenguiya Romarick Mondzali,² Yeto Emmanuel Mampouya Wenina,² Brice Chérubins Ouissika,² and Loumeto Jean Joel³

¹ENS, Département de Sciences et Vie de la terre, Université Marien Ngouabi, BP 69, Brazzaville, Congo
²ENSAF, Laboratoire d’Ecologie Appliquée Université Marien Ngouabi, BP 69, Brazzaville, Congo
³Faculté des Sciences, Département de Biologie et Physiologie Végétales, Université Marien Ngouabi, Brazzaville, Congo
⁴Via Costantino Beltrami 2, 00154 Roma, Italy

Received 11 December 2015; Revised 24 April 2016; Accepted 30 May 2016

Academic Editor: Timothy Martin

Copyright © 2016 Suspense Averti Ifo et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Trees species diversity, richness, and similarity were studied in fifteen plots of the tropical rainforests in the northeast of the Republic of Congo, based on trees inventories conducted on fifteen 0.25 ha plots installed along different types of forests developed on terra firma, seasonally flooded, and on flooded terra. In all of the plots installed, all trees with diameter at breast height, DBH ≥ 5 cm, were measured. The Shannon diversity index, species richness, equitability, and species dominance were computed to see the variation in tree community among plots but also between primary forest and secondary forest. A total of 1611 trees representing 114 species and 35 families were recorded from a total area of 3.75 ha. Euphorbiaceae was the dominant family in the forest with 12 species, followed by Fabaceae-Mimosoideae (10 species) and Phyllanthaceae (6 species) and Guttiferae (6 species). The biodiversity did not vary greatly from plot to plot on the whole of the study area (3.75 ha). The low value of Shannon index was obtained in plot 11 () whereas the highest value was obtained in plot 12 (). The values of this index vary from 0.23 to 0.95 in plots P11 and P15, respectively. Results obtained revealed high biodiversity of trees of the forest of Impfondo-Dongou. The information on tree species structure and function can provide baseline information for conservation of the biodiversity of the tropical forest in this area.

1. Introduction

Tropical forests are the subject of several studies to better understand the role they could play in sustainable development, climate change, and floristic biodiversity [1, 2]. Tropical forests provide many goods and ecosystem services, such as prevention of soil erosion and preservation of habitats for plants and animals [3]. Globally, 52% of the total forests are in tropical regions and they are known to be the most important areas in terms of biodiversity [2, 4]. This diversity is an indicator that allows appreciating links between the richness and the abundance of individuals’ trees; it reflects the degree of heterogeneity or stability of vegetation [5]. In the Republic of Congo (RoC), according to the definition of the forest, forests cover 69% of the territory [6]. Sustainable management of these forests requires a good knowledge of all the natural forest resource; this knowledge could be reliable only through studies of the forest environment. Vegetation’s studies led to either conducting a physiognomic research of the architectural type or identifying a number of representative reporting vegetation parameters, allowing defining simply, in order to compare it to other vegetation (Lescure, 1985). For the present study, the second approach was used, that of the floristic and structural parameters.

Many tropical forests are under great anthropogenic pressure and require management interventions to maintain the overall biodiversity, productivity, and sustainability [7]. Understanding tree composition and structure of forest is a vital instrument in assessing the sustainability of the forest, species conservation, and management of forest ecosystems [8]. Long-term biodiversity conservation depends basically on the knowledge of the structure, species richness, and the ecological characteristics of vegetation.

Some studies on the knowledge of the plant resource were conducted in Republic of Congo ([9–14] for the massif of Mayombe, [15]), but these studies remained generally piecemeal and predominantly localized inner protected areas and logging forest concessions. These studies were related to the ethnobotanical aspects and general knowledge of the flora of the Republic of Congo. And most of these studies were done essentially in the south of Republic of Congo and just one in the centre-west of our country. This work will provide more information on the tropical forest of Likouala, RoC. The aims of this research paper are to identify and quantify tree forest species of the tropical rainforest of Likouaka and specific objectives are (i) a floristic analysis of the forest of the axis Impfondo-Dongou, Likouala; (ii) analysis of floristic heterogeneity between interforest plots.

The study area is located within the Likouala department, which is of the most important forest regions in Republic of Congo.

2. Material and Methods

2.1. Study Area

The study was carried out within the tropical rainforest of the North of Congo Brazzaville in the department of Likouala (Figure 1). The zone of study covers a total surface of 155274 ha. It lies between 1°27′52,85′′ and 2°6′55,76′′ of northern latitude and between 17°52′35,04′′ and 18°04′32,65′′ of longitude.

Figure 1: Localization of the department of Likouala, Congo Brazzaville.

The climate of the study area is of equatorial type. Mean rainfall is of 1760 mm y⁻¹, with a dry season from December to January and a long wet season from March to November (Figure 2). In the Dongou district, the soil cover is of tertiary clay sandy formation and a quaternary alluvial formation to the east. The soils derived from there are impoverished ferrilitic brown-red clay-sand soils on the Western plateau, ferralitic/hydromorphic alluvial soils on alluvial terraces, and waterlogged peat soils in flooded areas. This area has one of the very low densities of human population (0.93 km⁻²) of the Republic of Congo. The forest of Likouala contains a high diversity of trees and plants [16]. In the Dongou district, the forests of the study area are rainforest. The principal vegetation types are partially deciduous dense rainforests of Ulmaceae and Sterculiaceae, swampy flooded forest of Uapaca heudelotii, and forest of Guibourtia demeusei [17]. Tree canopy closure of the forest varies from 93% to 100% while the tree height varies from 30 m to above 45 m (own data).

Figure 2: Ombrothermic diagram of Likouala (data from 1932 to 2015), ANAC Congo.

2.2. Data Collection

The tree sampling for the data collection was performed in 15 plots of 50 m × 50 m each placed in different forest strata of the study area: primary forest, secondary forest, and a mosaic of primary and secondary forest (Figure 3). Table 1 indicates the distribution of plots on the extent of the zone of study. The plot of intact forests and degraded forests inventoried was selected after image processing Landsat (OLI 8) of the study area. Coordinates GPS of the zones chosen on the satellite images were recorded in a GPS and on the ground we used the function Goto to go towards the points selected for the installation of the plot of inventories. The ground data allowed validating the classification of different type of forest in primary forest and secondary or degraded forest but also of the forest agro plot. Four plots fell into the zone from forest degraded, ten plots fell in the primary forest, and 1 plot fell into an agro drill forest.

Table 1: Distribution of number of plots inside each type of forest.

Type of forest
Plots
Number of trees
Density (n/ha)
G (m²/ha)

DF¹⁢

67
268
6.75

73
312
9.11

212
848
34.24

217
868
26.73

PF 2⁢

115
460
23.06

103
412
25.88

64
256
36.37

70
280
30.80

36
144
16.01

115
460
29.20

133
532
36,38

132
528
29.51

162
648
35.54

121
484
21.60

AF³

51
204
36.52

1: degraded forest; 2: primary forest; 3: agroforestry.

Figure 3: Cartography of land use change inside study’s area.

GPS points of all plots were recorded, and inside each plot all living trees with diameter at breast height (DBH) ≥ 5 cm were recorded by species using latest botanical classification. All tree species were assigned to families and relative diversity (number of species in a family) was obtained for tree species diversity classification.

2.3. Measuring Biodiversity

We apply the Shannon diversity index () as a measure of species abundance and richness to quantify diversity of the woody species. This index takes both species abundance and species richness into account:

where equals the number of species and equals the ratio of individuals of species divided by all individuals of all species. The Shannon diversity index ranges typically from 1.5 to 3.5 and rarely reaches 4.5 [18].

The variance of is calculated by

and a -statistic to test the significant differences between two plots or samples as

where is the Shannon diversity index of sample .

Degrees of freedom for this test are equal to

where and are the number of individuals in samples 1 and 2, respectively [19]. We have also considered the Simpson index (), a measure of species dominance, and the Shannon diversity index (), a measure of evenness of spread.

The Simpson index is defined as

where is the number of individuals in the species and equals the total number of individuals. As biodiversity increases, the Simpson index decreases. Therefore to get a clear picture of species dominance, we used .

The Shannon-Wiener index is defined as

is the natural logarithm of the total number of species. A value for evenness approaching zero reflects large differences in abundance of species, whereas an evenness of one means all species are equally abundant:

where is the total number of species, “” is the number of individuals, and “” is the natural logarithm.

2.4. Similarity

The Jaccard index was used to calculate similarities of species between the forest types in different forest fragments. These coefficients are used to measure the association between samples. The similarity of two samples (floristic sample) is based on the presence or absence of certain species in the two samples [20]. To study the similarity of our different floristic samples, we used two binary factors excluding the double zeros, that is, the coefficient of Sorensen () and the coefficient of Jaccard (). The Sorensen coefficient provides a twice higher weight to double presence; we can consider the presence of a more informative than this absence [20]:

with = number of common presences for both floristic samples, = number of presences in the first floristic sample, = number of presences in the second floristic sample, and = number of species absent in both floristic samples.

According to L. Legendre and P. Legendre [20], the Sorensen coefficient is fully compared with the Jaccard coefficient; that is, if the similarity of a pair of objects computed by the Jaccard coefficient is higher than the similarity of another pair of objects, it will also be higher if we use the coefficient of Sorensen for the calculation of similarity.

3. Results

3.1. Floristic Composition and Species Richness

A total of 1611 trees representing 114 species and 35 families were identified from the total area (3.75 ha). Euphorbiaceae was the dominant family in the forest with 12 species, followed by Fabaceae Mimosoideae with 10 species. In terms of the number of trees individuals per family, Euphorbiaceae was the dominant in the whole forest with 239 trees, followed by Urticaceae with 235 trees (Table 2).

Table 2: Floristic lists and their frequencies of the study area.

Family
Scientific name
Number of species
Number of trees

Achariaceae
Caloncoba welwitschii (Oliv.) Gilg.
1
9

Anacardiaceae
Pseudospondias microcarpa (A. Rich.) Engl.
2
14

Trichoscypha acuminata Engl.

Annonaceae
Anonidium mannii (Oliv.) Engl. & Diels
2
19

Monodora angolensis Welw.

Apocynaceae
Alstonia boonei De Wild.
1
1

Aptandraceae
Ongokea gore (Hua) Pierre
1
1

Bignoniaceae
Markhamia tomentosa (Benth.) K.
1
1

Burseraceae
Dacryodes pubescens (Verm.) Lam.
1
3

Cannabaceae
Celtis adolfi-friderici Engl.
1
12

Chrysobalanaceae⁢
Parinari congensis F. Didr.
4⁢
32⁢

Parinari congolana T. Durand et H. Durand

Parinari excelsa Sabine

Maranthes glabra (Oliv.)

Combretaceae
Terminalia superba Engl. et Diels.
1
3

Ebenaceae
Diospyros crassiflora Hiern
2
47

Diospyros ituriensis (Gùrke) R. Let et F. White

Euphorbiaceae⁢
Cleistanthus itsogohensis Pellegr.
12⁢
239⁢

Croton haumanianus J. Léonard

Dichostemma glaucescens Pierre

Grossera macrantha Pax

Macaranga barteri Mull.-Arg.

Macaranga monandra Mull.-Arg.

Macaranga schweinfurthii Pax

Macaranga spinosa Mull.-Arg.

Plagiostyles africana (Mull.-Arg.) Prain

Ricinodendron heudelotii (Baill.) Pierre ex Pax

Sapium ellipticum (Hochst.) Pax

Tetrorchidium didymostemom (Baill.) Pax & K. Hoffm.

Fabaceae-Caesalpinioideae⁢
Copaifera salikounda Heckel
5⁢
116⁢

Daniellia pynaertii De Wild.

Dialum pachyphyllum Harms

Guibourtia demeusei (Harms) Léon.

Swartzia Bobgunnia fistuloides (Harms) G.H Kirkpr.

Fabaceae-Faboideae⁢
Angylocalyx pynaertii De Wild.
4⁢
123⁢

Baphia dewevrei De Wild.

Millettia sanagana Harms

Pterocarpus soyauxii Taub.

Fabaceae-Mimosoideae
Albizia ferruginea (Guill. & Perr.) Benth.
10
58

Albizia laurentii De Wild.

Cathormion rhombifolium (Benth.) Hutch. & Dandy (syn: Albizia rhombifolia Benth.)

Albizia zygia (DC) J. F. Macbr.

Newtonia devredii G. C. C. Gilbert

Parkia filicoidea Welw. ex Oliv.

Parkia bicolor A. Chev.

Pentaclethra macrophylla Benth.

Piptadeniastrum africanum (Hook. F.) Bren.

Tetrapleura tetraptera (Schum. & Thonn.) Taub.

Guttifereae
Allanblackia floribunda Oliv.
6
55

Garcinia punctata Oliv.

Garcinia ovalifolia Oliv.

Mammea africana Sabine

Symphonia globulifera L. f.

Garcinia smeathmannii Oliv.

Irvingiaceae
Irvingia excelsa
3
16

Irvingia grandifolia (Engl.) Engl.

Klainedoxa gabonensis Pierre ex Engl.

Lamiaceae-Viticoideae
Vitex pachyphylla Bak.
1
8

Lauraceae
Persea americana L.
1
1

Lecythidaceae
Petersianthus macrocarpus (P. Beauv.) Liben.
2
63

Brazzeia congensis Baill.

Malvaceae-Sterculioideae
Cola nitida (Vent.) Schott & Endl.
1
2

Malvaceae-Tilioideae
Duboscia macrocarpa Brocq.
1
8

Meliaceae
Carapa procera var. palustre DC
5
46

Carapa procera var. procera DC

Entandrophragma cylindricum (Sprague) Sprague

Trichilia monadelpha (Thonn.) J. J. De Wild.

Trichilia tessmannii Harms

Moraceae
Antiaris toxicaria var. welwitschii Lesch.
5
17

Ficus exasperata Vahl.

Ficus vogeliana (Miq.) Miq.

Milicia excelsa (Welw.) C. C. Berg

Trilepisium madagascariense DC.

Myristicaceae
Coelocaryon preussii Warb.
3
226

Pycnanthus angolensis (Welv.) Exell

Staudtia kamerounensis Warb. var. gabonensis Fouilloy

Ochnaceae
Lophira alata Banks ex Gaertn.
2
14

Rhabdophyllum welwitschii Van Tiegh.

Olacaceae
Heisteria parvifolia Smith
3
52

Strombosia grandifolia Hoof. F.

Strombosia pustulata Oliv.

Pandaceae
Panda oleosa Pierre
1
6

Passifloraceae
Barteria fistulosa Mast.
1
1

Putranjivaceae
Drypetes pellegrini Léandri
2
7

Drypetes leonensis (Pax) Pax et K. Hoffm.

Phyllanthaceae
Cleistanthus mildbraedii Jabl.
6
37

Hymenocardia ripicola J. Léonard

Hymenocardia ulmoides Oliv.

Maesobotrya dusenii (Pax) Hutch.

Uapaca guineensis Mull.-Arg.

Uapaca heudelotii Baill.

Rubiaceae
Aidia micrantha (K. Schum.) F. White
5
44

Colleactina papalis N. Hallé

Massularia acuminata (G. Don) Bullock ex Hoyle

Morelia senegalensis A. Rich.

Morinda pynaertii Benth.

Oxyanthus schumannianus De Wild. et Th. Dur

Psydrax subcordata DC

Psydrax arnoldiana (De Wild.)

Rutaceae
Zanthoxylum heitzii (Aubrév. & Pellegr.) P. G. Waterman
1
1

Sapindaceae
Blighia welwitschii (Hiern) Radlk.
4
55

Eriocoelum microspermum Radlk.

Lecaniodiscus cupanioides Planch. ex Benth.

Pancovia pedicellaris Radlk. & Gilg

Sapotaceae
Chrysophyllum beguei Aubrév.
4
18

Synsepalum brevipes (Baker) TD Penn

Tridesmostemom omphalocarpoides Engl.

Manilkara sp.

Manilkara fouilloyana Aubr. et Pellegr.

Thomandersiaceae
Thomandersia hensii De Wild.
1
21

Urticaceae
Musanga cecropioides R. Br.
2
235

Myrianthus arboreus P. Beauv.

Total
114
1611

In terms of characterization of forest type, this inventory allowed distinguishing several forest types like Lophira alata, Uapaca heudelotii, Guibourtia demeusei, and Celtis adolfi-friderici. Inventories have revealed the existence of three vertical strata, whose upper stratum is dominated by species referred to above.

The biodiversity did not vary greatly from plot to plot on the whole of the study area (3.75 ha). A low Shannon diversity index value was obtained in plot 11 () whereas the highest value was obtained in plot 12 (). A statistical analysis made by launched ANOVA revealed that plot 11 was significantly different to the other plots (). A great difference was also noted in biodiversity between secondary plots and primary plots (Table 3). The evenness index was calculated. The values varied from 0.23 in plot P11 to 0.95 in plot P15.

Table 3: Biodiversity values by biodiversities index and static parameters.

Plots
Type of forest
Total individual
S
Shannon diversity index ()
Fisher’s α
Simpson index
Evenness index =
Variances ()
Ecartype

Degraded forest
67
26
4.33
15.76
0.05
3.06
0.28
0.53

Degraded forest
79
22
3.54
13.99
0.14
2.64
0.18
0.43

Degraded forest
212
38
4.13
23.23
0.08
2.62
0.09
0.3

Primary forest
132
26
3.57
14.92
0.14
2.52
0.11
0.34

Primary forest
111
24
3.97
11.3
0.08
2.88
0.15
0.39

Primary forest
102
29
4.14
17.39
0.07
2.83
0.18
0.42

Primary forest
52
15
3.36
8.39
0.11
2.86
0.23
0.48

Primary forest
61
9
2.46
3.81
0.22
2.58
0.11
0.33

Primary forest
34
12
2.93
8.13
0.16
2.72
0.28
0.53

Primary forest
106
27
3.94
16.32
0.09
2.76
0.16
0.4

Degraded forest
217
10
0.75
5.85
0.05
0.75
0.04
0.2

Primary forest
126
33
4.47
17.76
0.05
2.94
0.16
0.41

Primary forest
153
31
3.89
19.03
0.1
2.61
0.11
0.33

Primary forest
109
31
4.38
16.54
0.06
2.93
0.18
0.43

Agroforestry
47
20
4.12
11.37
0.04
3.17
0.36
0.6

The evenness index was calculated for each plot. The value of equitability varied from 0 to 1. It is equal to 1 when all the species have same abundance and tend towards 0 when the near total of flora is concentrated on only one species. The values of this index varied from 0.23 to 0.95 in plots P11 and P15, respectively (Figure 4). The value of plot 11 confirms well conducted survey in the plot which is dominated by one species, Musanga cecropioides. The value obtained in plot P11 is the one with a value inferior to 0.5 out of the entire results. Two plots have value of superior to 0.9 (plots P1 and P15). Twelve plots have a value of varying between 0.7 and 0.89.

Figure 4: Shannon diversity index and evenness index trends in all the study areas.

3.2. Biodiversities Indexes and Other Parameters

Other analyses of the biodiversity made by applying the other indices such as the index of Fisher revealed interesting information. Whereas with the Shannon diversity index, it is in plot 11 that we noted the weakest biodiversity, the application of the index Fisher (Table 3) showed that the low value of the biodiversity was obtained in plot 08 which is a primary forest plot whereas the strongest value of is observed in P3 plot, which is a mosaic of secondary and primary forest. Plot 11 (monodominant plot of Musanga cecropioides) does not have the low value of the biodiversity like Shannon diversity index revealed.

The species richness of 114 species was observed in 3.75 ha of the Likouala Forest Department. Musanga cecropioides was the most dominant with 222 trees censured followed by Staudtia kamerounensis var. gabonensis with 117 trees.

3.3. Similarity: Sorensen () and Jaccard () Index

Species similarities between the forest types were studied between primary forest and secondary forest (FS-FP), primary forest and agroforestry land (AF-FP), and agroforestry land and secondary forest (plot 15). We have noted that the lowest Jaccard index value was obtained between AF-FP (Figure 5) (17.18%). The highest value was noted between FS-FP.

Figure 5: Similarity index between two types of forest. AF = agroforestry, FP = primary forest, and FS = secondary forest.

The indices of diversity enabled us to conclude that the studied zones are rich in cash. Are various studied forests similar from the floristic composition point of view?

The values of coefficient of similarity vary from 17.18% to 28.48% for the index of Jaccard and 29.33% to 44.33% for the index of Sorensen.

4. Discussion

The analysis of the tree flora of the study area showed that the families of Euphorbiaceae (10.53%) are the most represented, followed by the Fabaceae-Mimosoideae (8.77%), Rubiaceae (7.89%), and the Guttiferae (6.14%). Indeed, the presence of the Euphorbiaceae and Rubiaceae generally represented by species of wood is a character common to all tropical rainforests as noted by Reynal-Roques [29]. However the abundance of the Fabaceae-Mimosoideae and Guttiferae is proof of the old age or maturity of the inventoried forest [11]. From the point of view of physiognomy of forest areas studied, the results show that these are the Euphorbiaceae (14.84%) which are abundant in terms of number of trees from beneath wood and stratum average, followed by the Urticaceae (14.59%), the Myristicaceae (14.03%) of the Fabaceae-Faboideae (7.64%), and Fabaceae-Mimosoideae (7.20%). The abundance of the Urticaceae is explained by the presence of quasi-monospecific stands to Musanga cecropioides in degraded forests. However the abundance of the Myristicaceae and Fabaceae is a specific character of the forests studied axis Impfondo-Dongou. Indeed, the results obtained in our study are totally different from those obtained by Kimpouni [22] in Congolese coastal forests, Koubouana et al. [30] in the forest of Western Centre at Mbomo and Kelle. Indeed the work of Kimpouni [22] performed in the littoral showed an abundance of the Fabaceae-Caesalpinioideae, followed by the Rubiaceae and Euphorbiaceae. Those of Koubouana et al. (in press) in the centre-west of the Congo showed an abundance of the Fabaceae-Caesalpinioideae (18.05%), followed by the Meliaceae (7.52%), Fabaceae-Mimosoideae (6.02%), Euphorbiaceae (5.26%), Annonaceae (4.51%), and the Myristicaceae (3.76%). In the study conducted at the Mayombe in the South of Congo by Koubouana et al. [21], the results obtained show an abundance of family Burseraceae (19.17%) followed by the Fabaceae-Caesalpinioideae (16.09%), Myristicaceae (13.18%), Annonaceae (9.49%), Euphorbiaceae (8.32%), and Fabaceae-Mimosoideae (7.32%). This variation of the floristic composition of the different forests studied is explained by the diversity of geological substrate and the diversity of climate (Table 4). Table 5 showed the characteristics of ecological factors in the forests studied.

Table 4: The characteristics of ecological factors in some forests of Republic of Congo.

Name of forest
Rainfall (mm)
Authors
Length of dry season

Forest of Impfondo-Dongou
1800–2000
Our study
2

Forest of Mayombe
1600
Koubouana et al. [21]

4

Forest of centre-west of Congo
2132.6
Our own data
2

Forests of the littoral
1500
Kimpouni [22]
4

Table 5: The characteristics of ecological factors in some forests of Republic of Congo.

Type of vegetation
Minimum tree DBH
Study area (ha)
Countries
Rainfall mean (mm/year)
Shannon-Wiener index (bit)
Number of families
Number of genera
Number of trees
Number of species
Authors

DBH ≤ 10 cm
1.5

1200–1500

47
120

153
Kimpouni et al. [23]

Forest
DBH ≥ 20 cm
35
Southwest of the Republic of Congo
1600
3.75
41

5076

 Koubouana et al. [21]

Shrub savannah

400
Plateaux Teke, Republic of Congo
1600–2100
2.16
15
16
3075
25
Mampouya Wenina [24]

Fabaceae-Caesalpinioideae
DBH ≥ 20 cm
88.5
Northwest of Republic of Congo
1900
5.3
31
107
11012
133
Koubouana et al. (in press)

Forest
DBH ≥ 10 cm

Plateau des Cataractes, Republic of Congo
1400–1600 mm

42
116

153
Kimpouni [22]

Forest (monodominant Aucoumea klaineana)
DBH ≥ 10 cm

Youbi
1200

1186
71
Kimpouni et al. [25]

Mosaics of natural forest and grassland
(DBH) ≥ 10 cm
0.72
Uganda,
Youbi, Republic of Congo (southwest)
1397–1500 mm
4.02
26

93
Nangendo et al. [26]

DBH ≥ 15 cm
1

1300
3.55, 3.47, 3.48, and 3.32
40
73
1789
92
Premavani et al. [27]

Forest
DBH ≥ 10 cm
1.96

2500–3000
3.795

808
72
Aigbe and Omokhua [28]

It is important to note that Brazzaville is in the south of the Republic of Congo and Mbomo-Kelle’s locality is in the northwest of Republic of Congo. In comparison with these two localities, our study area is in the extreme northeast. Each of the study areas has a local climatic condition (Table 4).

Table 3 shows the values for the assessment of the biodiversity of trees surveyed in 15 parcels that were the subject of this study on floristic biodiversity on ≥10 cm DBH trees. In this study we wanted to focus our attention on the biodiversity indices to assess the level of biodiversity across the study area, but also the microvariations that would exist between the plots of the study area. Moreover, in the scope of this study, we tested the role that vegetation indexes might play in the evaluation of forest degradation between primary and secondary forests.

Considering the Shannon diversity index, our study showed that plot 15 has a lower Shannon index of 1, while two plots have clues to Shannon between 2 and 3. The rest of the plots with higher values have 3. High species richness is a hallmark of many tropical forests (Gentry et al. 2010).

Our study revealed the existence of variability of biodiversity in the study area. According to Orth and Colette [31] the Shannon diversity index has strong values for species with recoveries of same importance and it takes low values, when some species have strong recoveries.

Low biological diversity noted in plot 11 () could be explained by the fact that it is dominated by a single species Musanga cecropioides. This species contributes nearly 90% of the total number of trees in the plot. In two plots with the highest values, the plots contain more than 30 species of trees with at least two species of codominant trees, but with lower contributions. In parcel 12 (), Angylocalyx pynaertii De Wild and Plagiostyles africana species each have a 13% contribution. In these same plots the other two species following in terms of specific contribution are Grossera macrantha and Strombosia grandifolia with, respectively, 7% and 6% of a total of 126 species inventoried in this plot. As shown in Table 1, the application of the other indices of biodiversity gives a different result. The Pioulou biodiversity index () indicates that plot 15 () has the highest biodiversity followed by plot 1 () and plot 12 (). Several causes could explain variations in the degree of biodiversity between the plots of the study area: soil type, rainfall trends, anthropogenic action, land use change, and so forth.

The Shannon diversity index values obtained in this study are lower than those obtained in other studies both in the Republic of Congo and in other tropical forests in the Congo basin compared to other tropical countries. For instance, in the forest of centre-west of Republic of Congo in Mbomo-Kelle (Republic of Congo), Shannon diversity index varies from 5.91 to 5.95 in bloc 4 and bloc 9, respectively (Koubouana et al. in press). In the southwest of the Republic of Congo, studies were conducted by Kimpouni et al. [23] and Koubouana et al. [21] and revealed different values. Kimpouni et al. [23] in a degraded forest in Brazzaville obtained for woody species a Shannon diversity index of 1.9 bits. But in the tropical forest of southwest of the Republic of Congo, Koubouana et al. (in press) noted an old secondary forest that the Shannon diversity index was about 3.08.

Regarding heterogeneity, many authors think that the structural heterogeneity of the forests and their high species richness are often interpreted in terms of forest dynamics and relationship with the resulting phenomena of succession [5, 32]. In this work, we have mainly focused on the study of the biodiversity of trees to make a comparison between the degraded forest areas and nondegraded forest areas.

Several factors could explain the variations of biodiversity in our study: the topography of the area [33, 34] or edaphic factors [35, 36] to explain the issue of floral heterogeneity of tropical forests. In our study area, three forest types were identified: flooded forests, solid ground forest, and partially flooded forest. In the context of this work we have studied the differences that exist between forest types through the Jaccard and of Sorensen similarity indexes. Moreover, () and Jaccard () index give a very good idea of the presence or absence of species in the different transects of the inventory. The range of this coefficient is between 0 and 1. Interpretation of the CSJ values is as follows: 1: both survey sites have only common species; 0: both survey sites have only singular species; 1/2: the two survey sites have as many common species as the sum of singular species at each survey site; [0, 1/2]: the similarity in terms of species diversity between both survey sites is rather low; [1/2.0]: the similarity in terms of species diversity between both survey sites is rather high.

In our case, it ranges from 17.18 to 23.48%, taking into account the three combinations (AF-FP, AF-FS, and FS-FP). This means the similarity in terms of species diversity between both survey sites is rather low. The results showed that there is a high tree biodiversity in our study area.

The values of similarity index are lower than 50%, which enables us to conclude that there is obviously a difference in point of floristic composition between the primary forests and the secondary forests, thus confirming the floristic data that we presented above.

4.1. Evaluation of Forest Degradation through the Biodiversity Indexes

Degradation is considered to be a temporal process. There is however a consensual definition that is accepted by the various stakeholders, which is as follows: forest degradation is the reduction of the capacity of the forest to provide goods and services. In the context of REDD+, forest degradation can be defined as the partial loss of biomass due to logging or other causes of removal of wood from biomass [37]. A degraded forest is a secondary forest that has lost, as a result of human activities, the structure, function, composition, or productivity of species normally associated with a natural forest. Thus, a degraded forest offers a supply of goods and services and has only limited biodiversity. Biological diversity in a degraded forest includes many nontree components which can dominate the understory vegetation cover (CBD (2005; 2001).

To assess the level of forest degradation, a maximum biodiversity index has been applied and presents different values between the secondary and primary forest. These forests are characterized by a very high biodiversity, especially in the case of secondary forests of Macaranga spinosa or Macaranga barteri. In the case of plots P1 and P2 the objective of this study is to identify settings that allow assessing forest degradation.

5. Conclusion

The study of the biodiversity of the Likouala forests and the Impfondo-Dongou axis revealed a high floral biodiversity of trees considering a diameter of 5 cm at DBH 1.30 m. Tree biodiversity is very important in primary forests. In secondary forests, the biodiversity varies in line with the secondary forest type: secondary forest of Macaranga spinosa or secondary forest of Musanga cecropioides. Moreover, biodiversity varies according to the nature of the substrate: forest on dry land, forest in partially flooded areas, and flooded forest.

Competing Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

The authors are thankful to GEOFORAFRI for funding the project. The authors thank Benoit Mertens for kind support during the project.

References

S. L. Lewis, G. Lopez-Gonzalez, B. Sonké et al., “Increasing carbon storage in intact African tropical forests,” Nature, vol. 457, no. 7232, pp. 1003–1006, 2009.

M. N. K. Djuikouo, J.-L. Doucet, C. K. Nguembou, S. L. Lewis, and B. Sonké, “Diversity and aboveground biomass in three tropical forest types in the Dja Biosphere Reserve, Cameroon,” African Journal of Ecology, vol. 48, no. 4, pp. 1053–1063, 2010.

M. Anbarashan and N. Parthasarathy, “Tree diversity of tropical dry evergreen forests dominated by single or mixed species on the Coromandel coast of India,” Tropical Ecology, vol. 54, no. 2, pp. 179–190, 2013.

L. R. Holdridge, “Life Zone Ecology, Tropical Science Center, San Jose, Costa Rica,” 1967

V. Trichon, “Hétérogénéité spatiale d'une forêt tropicale humide de Sumatra: effet de la topographie sur la structure floristique,” Annales des Sciences Forestières, INRA/EDP Sciences, vol. 54, no. 5, pp. 431–446, 1997.

CNIAF, “Carte de Changement de Couverture Forestière en République du Congo pour la Période 2010–2012,” 2015

A. Kumar, B. G. Marcot, and A. Saxena, “Tree species diversity and distribution patterns in tropical forests of Garo Hills,” Current Science, vol. 91, no. 10, pp. 1370–1381, 2006.

D. S. Kacholi, “Analysis of structure and diversity of the Kilengwe Forest in the Morogoro Region, Tanzania,” International Journal of Biodiversity, vol. 2014, Article ID 516840, 8 pages, 2014.

J.-M. Moutsambote, Dynamique de reconstitution de la forêt Yombe (Dimonika, R.P. du Congo) [Ph.D. thesis], These de 3e cycle, University of Bordeaux, Bordeaux, France, 1985.

G. Cusset, La Flore et la Végétation du Mayombe Congolais. État des Connaissances, Université Pierre et Marie Curie, Paris, France, 1987.

G. Cusset, “La flore et la végétation du Mayombe congolais, état des connaissances,” in Revue des Connaissances sur le Mayombe, J. Sénéchal et al., Ed., pp. 103–136, Unesco, Paris, France, 1989.

E. J. Adjanohoun, A. M. R. Ahyi, L. AkeAsi et al., Contribution aux Études Ethnobotaniques et Floristiques en République Populaire du Congo: Médecine Traditionnelle et Pharmacopée, ACCT, Paris, France, 1988.

V. Kimpouni and F. Koubouana, “Étude ethnobotanique sur les plantes médicinales et alimentaires dans et autour de la réserve de Conkouati,” Rapport Final, PROGECAP/GEF-Congo, UICN, 1997.

F. Dowsett-Lemaire, “The vegetation of the Kouilou basin in Congo,” in Flore et Faune du Bassin du Kouilou (Congo) et Leur Exploitation, R. J. Dowsett and F. Dowsett-Lemaire, Eds., vol. 4, pp. 17–51, Tauraco Research Report, 1991.

F. Koubouana and J. M. Moutsambote, Etude Préliminaire de la Végétation de l'UFA Letili et Bambama, Rapport D’étude, Brazzaville, Congo, 2006.

J.-M. Moutsamboté, Etude écologique, phytogéographique et phytosociologique du Congo septentrional (Plateaux, Cuvettes, Likouala et Sangha) [Thèse de Doctorat d'Etat], Faculté des Sciences, Université Marien Ngouabi, Brazzaville, République du Congo, 2012.

IUCN, “La conservation des ecosystèmes forestiers du Congo. Basé sur le travail de Philippe Hecketsweiller. IUCN, Gland, Suisse et Cambridge, Royume uni. 187., illustré,” 1989

W. L. Gaines, J. R. Harrod, and J. F. Lehmkuhl, “Monitoring biodiversity: quantification and interpretation,” General Technical Report PNW-GTR-443, USDA Forest Service, Pacific North-West Research Station, 1999.

A. E. Magurran, Ecological Diversity and Its Measurement, CroomHelm, London, UK, 1988.

L. Legendre and P. Legendre, Écologie Numérique, Tome 1: Traitement Multiple des Données Écologiques, Masson, Paris, France, 2nd edition, 1984.

F. Koubouana, S. A. Ifo, J.-M. Moutsambote et al., “Structure and flora tree biodiversity in congo basin: case of a secondary tropical forest in southwest of congo-brazzaville,” Research in Plant Sciences, vol. 3, no. 3, pp. 49–60, 2015.

V. Kimpouni, “Contribution to the inventory and analysis of the ligneous flora of the plates of the Cataracts (Congo-Brazzaville),” Acta Botanica Gallica, vol. 156, no. 2, pp. 233–244, 2009.

V. Kimpouni, Å. Apani, and M. Motom, “Analyse phytoécologique de la flore ligneuse de la Haute Sangha (République du Congo),” Adansonia, Série 3, vol. 35, no. 1, pp. 107–134, 2013.

Y. E. Mampouya Wenina, Biodiversité et variabilité de la densité du bois des arbustes de savane dans les environs du village Mâh (Plateaux TEKE, République du Congo) [M.S. thesis], Université Marien Ngouabi, 2015.

V. Kimpouni, J. Loumeto, and J. Mizingou, “Woody flora and dynamic of Aucoumea klaineana forest in the Congolese littoral,” International Journal of Biological and Chemical Sciences, vol. 8, no. 4, pp. 1393–1410, 2014.

G. Nangendo, A. Stein, M. Gelens, A. de Gier, and R. Albricht, “Quantifying differences in biodiversity between a tropical forest area and a grassland area subject to traditional burning,” Forest Ecology and Management, vol. 164, no. 1–3, pp. 109–120, 2002.

D. Premavani, M. T. Naidu, and M. Venkaiah, “Tree species diversity and population structure in the Tropical Forests of North Central Eastern Ghats, India,” Notulae Scientia Biologicae, vol. 6, no. 4, pp. 448–453, 2014.

H. I. Aigbe and G. E. Omokhua, “Tree species composition and diversity in Oban Forest reserve, Nigeria,” Journal of Agricultural Studies, vol. 3, no. 1, pp. 10–24, 2015.

Reynal-Roques, La Botanique Redecouverte, Reynal-Roques, Berlin, Germany, 1994.

F. Koubouana, S. A. Ifo, J.-M. Moutsambote, and R. Mondzali-Lenguiya, “Floristic diversity of forests of the Northwest Republic of the Congo,” Open Journal of Forestry, In press

D. Orth and M. G. Colette, “Espèces dominantes et biodiversité: relation avec les conditions édaphiques et les pratiques agricoles pour les prairies des marais du cotentin,” Ecologie, vol. 27, no. 3, pp. 171–189, 1996.

A. Aubréville, “La forêt coloniale: les forêts de l'afrique occidentale française,” Annales—Académie des Sciences Coloniales, vol. 9, pp. 1–245, 1938.

F. Kahn, Architecture comparée de forêts tropicales humides et dynamique de la rhizosphère [Ph.D. thesis], USTL, Montpellier, France, 1983.

K. Basnet, “Effect of topography on the pattern of trees in tabonuco (Dacryodes excelsa) dominated rain forest of Puerto Rico,” Biotropica, vol. 24, no. 1, pp. 31–42, 1992.

J.-P. Lescure and R. Boulet, “Relationships between soil and vegetation in a tropical rain forest in French Guiana,” Biotropica, vol. 17, no. 2, pp. 155–164, 1985.

J. S. Gartlan, D. M. Newbery, D. W. Thomas, and P. G. Waterman, “The influence of topography and soil phosphorus on the vegetation of Korup Forest Reserve, Cameroun,” Vegetatio, vol. 65, no. 3, pp. 131–148, 1986.

M. Kanninen, D. Murdiyarso, F. Seymour, A. Angelsen, S. Wunder, and L. German, Do Trees Grow on Money? The Implications of Deforestation Research for Policies to Promote REDD, Forest Perspectives no. 4, CIFOR, Bogor, Indonesia, 2007.