Submit manuscript...
International Journal of
eISSN: 2574-9862

Avian & Wildlife Biology

Research Article Volume 7 Issue 2

Forest Structure, Tree Species Diversity, and Distribution in Ukpon River Forest Reserve, Cross River State, Nigeria

Esor PE,1 Amonum JI,2 Agera SIN2

1Department of Forestry and Wildlife Management, Cross River University of Technology Calabar, NIgeria
2Department of Forest Production and products, College of Forestry and Fisheries, Joseph Sarwuan Tarka University Makurdi, Nigeria

Correspondence: Esor PE. Department of Forestry and Wildlife Management Cross River University of Technology Calarba, Nigeria, Tel +234 (0)8068347777

Received: February 24, 2023 | Published: May 4, 2023

Citation: Esor PE, Ammonum JI, Agera SIN. Forest Structure, Tree Species Diversity, and Distribution in Ukpon River Forest Reserve, Cross River State, Nigeria. Int J Avian & Wildlife Biol. 2023;7(2):46-54. DOI: 10.15406/ijawb.2023.07.00189

Download PDF

Abstract

For effective conservation management, it is crucial to comprehend the diversity, abundance, and distribution of the forest as wildlife habitat. The fundamental composition of the forest is significantly influenced by the ecological features of the sites, species diversity, and rate of tree species regeneration. This finding aimed to assess the diversity, abundance, and distribution of tree species as suitable habitat for wildlife species and for sustainable forest management, climate change mitigation, and environmental resilience. The study was conducted in dry season (between 5th September, 2021 and April, 2022). Purposive sampling techniques and systematic line transects were used for data collection and plot delineation. There were laid 8 transects, each 1000 meters long and 500 meters apart. Descriptive statistics such as mean, frequencies, and percentages were used to analyze the data. Correlation analyses and diversity indices were carried out using the R programming software. In the study area, 68 tree species from 34 families were found. Meliacea (6 trees per ha), Caesalpiniceae, and Moracea (5 trees per ha) were the three most common tree species in the study area. Melicia excelsa showed the highest relative frequency (2.256%) and (2.241%). The species Bialonella toxisperma had the highest relative dominance (4.970%). In Melicia excelsa, IVI recorded the highest value (4.970%). The tallest tree and Dbh (Diameter at Breast Height) measured 80.5 cm and 68.3m). The Margelef index was 36.10, the Shannon Wiener index was 5.058, and species richness was 68. However, the high proportion of smaller-diameter trees in the forest reserve implies that, it is strong and healthy. Since natural areas play a critical role in slowing down climate change, strict oversight of these areas should be strongly encouraged.

Keywords: tree species, diversity, distribution, abundance, okpon river

Introduction

Understanding the forest stands' structure, diversity, abundance, and distribution is essential for conservation management. The ecological characteristics of the sites, species diversity, and the rate of tree species regeneration all play a significant role in the fundamental structure of the forest. Tree species abundance and diversity are essential to the overall biodiversity of forests because trees provide resources such as food, traditional medicine, timber, shade, and habitats for fauna Sushma et al.,1 Due to numerous anthropogenic factors, the extent of species decline in the second half of the 20th century became a universal or global problem.2 The provision and protection of biodiversity services are crucial to describing the pattern of forest structure in order to control or manage the increasing rate of anthropogenic activities within the forest estate.3 The variation in tree species diversity among forest reserves has been attributed to a variety of factors. According to Malhil et al.,4 and Lippok et al.,5 topography has a significant impact on the local endemism of plant species. Franscico et al.,  reported that disturbance has an impact on diversity and regeneration, including changes in tree growth, tree mortality, understory development in relation to forest reserves, and habitat heterogeneity. Forests are one of the main vegetative elements in India (as well as Nigeria), and they serve as a priceless repository for numerous economically significant species as well as the genetic material for many crop plants and their wild relatives.5 Basic understanding of key elements' spatial and temporal ranges as well as the main environmental factors that influence their survival and distribution is necessary for sustainable conservation management.6

Material and methods

The study area

Okpon River Forest Reserve was gazetted by  Cross River State in 1930. The reserve occupied a land mass of 31,300 hectares, covering two local government areas, Obubra and Yakurr, respectively. The Reserve lies between Latitudes 50 . 401 ,50.501 and 60.001,  60 .101 North of the Equator and Longitude  80. 101 ,80. 20and 80.301 ,  80. 401 East of the Greenwich Meridian   Figure 1. The reserve is bounded in the north by Etung and Ikom LGAs, south by Baise LGA, west by Abi LGA, and east by Eboyi State.

Figure 1 Map of Okpon river forest reserve.

Sampling techniques/procedure

Transects and plots were selected using systematic and purposeful sampling techniques. For the purpose of counting the species of plants, eight (8) transects were set up. At regular intervals of 250 m along the transects, four plots of 50 m x 50 m (0.25 ha) size were systematically placed alternately along each transect. A hundred metres separated each transect. All woody plants with a diameter at breast height (dbh) less than 10 cm were the only ones eligible for measurement and identification.

Data collection and analyses

The study was conducted in dry season (between September, 2021 and April, 2022). Data collected was based on Dbh (≥10 cm). The height of each individual tree was measured using a sunto clinometer, while the diameter of the trees was measured using a diameter tape. The diameter at breast height (> 10 cm dbh), importance value index (IVI), relative frequencies, relative dominance, relative density, and height of the entire individual tree were all calculated.

The 2017 version of the Microsoft Word and Excel package was used to impute the collected data. We used descriptive statistics like means, percentages, tables, and charts. Using diversity indices, the RF, RD, RDO, and IVI of tree species were calculated. The threshold for statistical significance was (P 0.005%). In the "R" software, correlation analysis and diversity indices were both carried out.

Basal areas: of all trees in the samples plots were calculated using the formula:

BA= π D 2 4 MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqkY=Mj0xXdbba91rFfpec8Eeeu0xXdbba9frFj0=OqFf ea0dXdd9vqaq=JfrVkFHe9pgea0dXdar=Jb9hs0dXdbPYxe9vr0=vr 0=vqpWqaaeaabiGaciaacaqabeaadaqaaqaaaOqaaiaadkeacaWGbb Gaeyypa0ZaaSaaaeaacqaHapaCcaWGebWaaWbaaSqabeaacaaIYaaa aaGcbaGaaGinaaaaaaa@3DE8@   (1)

B.A= Basal Area (m2), D= Diameter at Breast Height (cm) and ᴨ =(3.142).

Species Relative density (RD %):

RD= ni×100 N MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqkY=Mj0xXdbba91rFfpec8Eeeu0xXdbba9frFj0=OqFf ea0dXdd9vqaq=JfrVkFHe9pgea0dXdar=Jb9hs0dXdbPYxe9vr0=vr 0=vqpWqaaeaabiGaciaacaqabeaadaqaaqaaaOqaaiaadkfacaWGeb Gaeyypa0ZaaSaaaeaacaWGUbGaamyAaiabgEna0kaaigdacaaIWaGa aGimaaqaaiaad6eaaaaaaa@40BE@   (2)

RD = Relative density of the species, ni = Number of individuals per species and N = Total number of all individual tree of all species in the entire population.  

Species Relative Dominance (%) was estimated using the following equation:

R D 0 = B α 1 ×100 B α n MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqkY=Mj0xXdbba91rFfpec8Eeeu0xXdbba9frFj0=OqFf ea0dXdd9vqaq=JfrVkFHe9pgea0dXdar=Jb9hs0dXdbPYxe9vr0=vr 0=vqpWqaaeaabiGaciaacaqabeaadaqaaqaaaOqaaiaadkfacaWGeb WaaSbaaSqaaiaaicdaaeqaaOGaeyypa0ZaaSaaaeaadaaeabqaaiaa dkeacqaHXoqydaWgaaWcbaGaaGymaaqabaGccqGHxdaTcaaIXaGaaG imaiaaicdaaSqabeqaniabggHiLdaakeaadaaeabqaaiaadkeacqaH XoqydaWgaaWcbaGaamOBaaqabaaabeqab0GaeyyeIuoaaaaaaa@49FD@   (3)

Ba1 = Basal area of individual tree belonging to the ith species and Ban = Stand basal area.

Shannon – wiener diversity index was calculated using the following equation:

H= 1=1 P 1 In( P 1 ) MathType@MTEF@5@5@+= feaagKart1ev2aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr 4rNCHbGeaGqkY=Mj0xXdbba91rFfpec8Eeeu0xXdbba9frFj0=OqFf ea0dXdd9vqaq=JfrVkFHe9pgea0dXdar=Jb9hs0dXdbPYxe9vr0=vr 0=vqpWqaaeaabiGaciaacaqabeaadaqaaqaaaOqaaiaadIeacqGH9a qpcqGHsisldaaeqbqaaiaadcfadaWgaaWcbaGaaGymaaqabaaabaGa aGymaiabg2da9iaaigdaaeqaniabggHiLdGccaWGjbGaamOBaiaacI cacaWGqbWaaSbaaSqaaiaaigdaaeqaaOGaaiykaaaa@4508@   (4)

H’ = Shannon diversity index, S = the total number of species in the community, P1= Proportion S (species in the family) made u to the ith spp and In = natural logarithm.  

Important Value Index:

IVI =RF+RD+RD  (5)

RD = Relative density of the species; RDO = relative dominance

Results

Forest Structure of the Ukpon River Forest Reserve

Table 1 shows the diameter of breast height and the total height of species at the Okpon Forest Reserve. The maximum and minimum diameters at the base were recorded as 80.5 cm and 10.1 cm, with a mean of 25.1 cm and SD of 13.2. The mean total height was 28.6 m, with a standard deviation of 14.1 m. A minimum total height of 5.2 and a maximum of 68.3 m, with a mean of 28.6 m, were recorded in the study area. The diameter distribution in Figure 2 revealed that tree species within the diameter at breast height (dbh) distribution ranged from 10 cm to 70 cm. Fifty-five (55) trees belonged to the Dbh class (10 cm to 20 cm) and were the most frequently occurring in the area, representing 47%. This was followed by trees in the diameter class of 20cm – 40cm with twenty five (25) trees/ha representing 17.10%. the least number of  stem (15tree/ ha) and  (10 trees/ha) falls under diameter class of  40cm – 50cm and 50cm to 60cm representing 11.1% and 5.0% respectively  while the least species within the diameter range of  60 cm > 70 cm represented 11.1 % and 5.0% respectively. Based on the result of this finding Figure 3, the total height of tree species in the study area ranged from 10 to 70 m. Forty trees (40/ha) belonged to the tree height class of 20–30 m, representing 35%, followed by the tree height class of 30–50 m, with 25 trees representing 39.4%. Similarly, 20 trees/ha falls between the height classes of 50 – 60m trees represented 12.8% of the entire tree species in the study location.  Ten trees belonged to the height class between 60 and 70  m, representing 7.6%, while 5 trees per ha belonging to the height classes of 10 to 20 m and > 70 m were in the range of 2.6 each.

Figure 2 Diameter at breast height distribution of tree species in Okpon river forest reserve.

Figure 3 Total height distribution of trees at the okpon river forest reserve.

 Parameters

Dbh (cm)

Ht (m)

Minimum

10.1

5.2

Max

80.5

68.3

Mean

25.1

28.6

Standard deviation

13.2

14.1

Sample Size

937

937

Table 1 Summary statistics of growth variables in Okpon river forest reserve

Tree species diversity and distribution in okpon river forest reserve

The results of this study recorded 248 tree species belonging to 55 families. Caesalpinaceae had the highest number of species (24 trees per ha), followed by Moraceae (20 trees per ha), Euphorbiaceae (15 trees per ha), Apocynaceae and Steculiaceae (12 trees per ha), Leguminocea (10 trees per ha), Annonaceae (9 trees per ha), and Rutaceae (8 trees per ha). These families were regarded as the most dominant in the forest reserve. Sapindaceae and Ebeneceae had 7 species each, Rubiaceae had 6 species, Mimosaceae and Ulmaceae 5 tree Sapotaceae and Anacardiaceae 4 species, Gentianaceae and Lauraceae families 3 species. Eleven families recorded two species, while twenty (20) families recorded one species each (Table 2).

Relative Frequency, Relative Density, Relative Dominance, and Importance Value Index (IVI) of Tree Species at Okpon Forestry Reserve

The result indicates that Brachystegia eurycoma and Melicia excelsa had the highest relative frequency of (2.266) followed by Khaya ivorensis (1.933%), Diospyros mespiliformis, Funtumia elastic, and Lophira alata, which recorded the same relative frequency of (1.826%). The least relative frequency of (0.107 %) were recorded  in 107 tree species Table 2. The results of the relative density of  tree species at the Okpon forestry reserve presented in Table 2 showed that Brahystegia erycoma recorded the highest relative density of (2.241%), closely followed by Khaya ivorensis and Milicia excelsa that recorded the same value (2.028%), Lophira alata (1.814%), and Entandrophragma utile (1.708%), while the least relative density of (0.107%) was recorded in ninety-six (96) tree species.

Milicia excelsa recorded the highest relative dominance (4.970%), followed by Piptadeniastrum africana (4.643%), and Brachystegia erycoma (3.089%). The least relative dominance was obtained in Kigela africana (0.016%). Brachystegia erycoma recorded the highest IVI of 10.66%, followed by Milicia excelsa (9.46%) and Khaya ivorensis (6.865%). The lowest IVI of 0.228% was in Ficus muccuso and Mansonia altissima (Table 2).

S/No

Species

Family

RF(%)

RD(%)

RDo(%)

IVI

1

Acioa pallescens

Chysobalana

0.322

0.32

0.177

0.819

2

Aeglopsis chevalieri

Rutaceae

0.43

0.427

0.268

1.125

3

Afrormosia elata

Leguminosae

0.644

0.64

0.312

1.597

4

Afrostyrax lepidophyllus

Styraceae

0.107

0.107

0.039

0.253

5

Afzelia  africana

Caesalpinaceae

0.322

0.32

0.267

0.909

6

Afzelia bella

Caesalpinaceae

0.322

0.32

0.295

0.937

7

Afzelia bipindensis

Leguminosae

0.43

0.427

0.161

1.018

8

Afzelia pachyloba

Caesalpinaceae

0.107

0.107

0.053

0.267

9

Albizia  lebbeck

Leguminosae

0.107

0.107

0.023

0.237

10

Albizia adianthitolia

Mimosaceae

0.107

0.107

0.027

0.242

11

Albizia ferruginea

Leguminosae

0.43

0.427

0.177

1.033

12

Albizia gummifera

Leguminosae

0.215

0.213

0.094

0.523

13

Albizia zygia

Leguminosae

0.43

0.427

0.333

1.19

14

Alchornea cordifolia

Euphorbiaceae

0.215

0.213

0.054

0.482

15

Alchornea laxiflora

Euphorbiaceae

0.43

0.427

0.085

0.942

16

Allanblackia floribunda

Cluciaceae

0.644

0.64

0.509

1.794

17

Allophylus africana

Sapindaceae

0.107

0.107

0.127

0.342

18

Alophyllus africanum

Sapindaceae

0.107

0.107

0.056

0.27

19

Alstonia boonei

Apocynaceae

0.967

0.961

0.969

2.896

20

Alstonia congensis

Apocynaceae

0.859

0.854

0.965

2.678

21

Amphimas pterocarpoides

Leguminosae

0.43

0.427

0.209

1.065

22

Angylocalyx oligophyllus

Leguminosae

0.43

0.427

0.279

1.136

23

Aningeria robusta

Sapotaceae

0.215

0.213

0.03

0.459

24

Anonidum mannii

Annonaceae

0.107

0.107

0.042

0.256

25

Anthocleista djalonesis

Gentianaceae

0.107

0.107

0.134

0.348

26

Anthocleista nobilis

Gentianaceae

0.107

0.107

0.032

0.246

27

Anthocleista vogelii

Gentianaceae

0.107

0.107

0.12

0.334

28

Anthonotha macrophylla

Caesalpinacea

0.107

0.107

0.101

0.315

29

Antiaris africana 

Apocynaceae

0.107

0.107

0.053

0.267

30

Antiaris toxicaria

Moraceae

0.644

0.64

0.216

1.501

31

Antiaris welwitschii

Moraceae

0.215

0.213

0.051

0.48

32

Antidesma laciniatum

Euphorbiaceae

0.215

0.213

0.097

0.525

33

Antrocaryon micraster

Anacardiaceae

0.107

0.107

0.017

0.231

34

Aubregrinia taiensis

Mimosaceae

0.215

0.213

0.037

0.466

35

Avicennia africana

Avienniaceae

0.43

0.427

0.209

1.066

36

Azadirachta indica

Meliaceae

0.322

0.32

0.192

0.835

37

Baillonella toxisperma

Sapotaceae

1.504

1.494

3.672

6.67

38

Balanites wilsoniana

Balanitaceae

0.322

0.32

0.147

0.789

39

Baphia maxima

Papiloniaceae

0.537

0.534

0.2

1.271

40

Baphia nitida

Papiloniaceae

0.537

0.534

0.247

1.318

41

Barteria fistulosa

Passifloraceae

0.215

0.213

0.036

0.464

42

Barteria nigritana

Passifloraceae

0.322

0.32

0.263

0.906

43

Beilschmiedia gaboonensis

Lauraceae

0.322

0.32

0.182

0.825

44

Beilschmiedia mannii

Lauraceae

0.107

0.107

0.042

0.256

45

Berlinia auriculata

Caesalpinaceae

0.215

0.213

0.164

0.592

46

Berlinia bracteosa

Caesalpinaceae

0.107

0.107

0.017

0.231

47

Blighia sapida

Sapindaceae

0.215

0.213

0.163

0.592

48

Blighia unijugata

Sapindaceae

0.215

0.213

0.098

0.526

49

Blighia welwitschii

Sapindaceae

0.107

0.107

0.032

0.246

50

Bombax buonopozense

Bombaceae

1.611

1.601

2.071

5.283

51

Bosqueia angolensis

Moraceae

0.537

0.534

0.339

1.41

52

Bosquiea phoberos

Moraceae

0.322

0.32

0.07

0.713

53

Brachystegia eurycoma

Caesalpinaceae

2.256

2.241

6.17

10.667

54

Brachystegia kennedy

Caesalpinaceae

0.107

0.107

0.115

0.33

55

Brachystegia nigerica

Leguminosae

1.289

1.281

3.089

5.659

56

Brenania brieyi

Rubiaceae

0.215

0.213

0.255

0.683

57

Bridelia atroviridis 

Euphorbiaceae

0.107

0.107

0.087

0.301

58

Bridelia ferruginea

Euphorbiaceae

0.322

0.32

0.188

0.831

59

Caloncoba glauca

Flacourtiaceae

0.537

0.534

0.231

1.301

60

Calpocalyx brevibracteatus

Mimosaceae

0.43

0.427

0.258

1.115

61

Calpocalyx spp

Mimosaceae

0.107

0.107

0.016

0.23

62

Carapa procera

Apocynaceae

0.43

0.427

0.171

1.027

63

Carpolobia alba

Apocynaceae

0.107

0.107

0.043

0.258

64

Carpolobia lutea

Apocynaceae

0.107

0.107

0.049

0.263

65

Casearia barteri

Salicaceae

0.107

0.107

0.053

0.267

66

Cassipourea congoensis

RPhizophoraceae

0.107

0.107

0.024

0.238

67

Ceiba pentandra

Bombaceae

1.826

1.814

2.635

6.275

68

Celtis mildbraedii

Ulmaceae

0.107

0.107

0.105

0.32

69

Celtis zenkeri

Ulmaceae

0.107

0.107

0.022

0.237

70

Chrysophyllum albidum

Sapotaceae

1.396

1.387

1.387

4.171

71

Chrysophyllum spp

Sapotaceae

0.215

0.213

0.15

0.579

72

Chrysophyllum subnudum

Sapotaceae

0.752

0.747

0.707

2.206

73

Chytranthus ellipticus

Sapindaceae

0.322

0.32

0.535

1.177

74

Cinnamomum zeylanicum

Lauraceae

0.43

0.427

0.186

1.043

75

Citrus spp

Rutaceae

0.644

0.64

0.178

1.463

76

Cleistanthus polystachyus

Euphorbiaceae

0.215

0.213

0.157

0.585

77

Cleistopholis patens

Annonaceae

0.215

0.213

0.08

0.508

78

Cola acuminate

Steruliaceae

0.537

0.534

0.169

1.239

79

Cola digitate

Steruliaceae

0.215

0.213

0.15

0.579

80

Cola gigantean

Steruliaceae

0.859

0.854

0.461

2.174

81

Cola heterophylla

Steruliaceae

0.322

0.32

0.296

0.939

82

Cola hispida

Steruliaceae

0.322

0.32

0.282

0.924

83

Cola nigerica

Steruliaceae

0.107

0.107

0.102

0.317

84

Cola nitida

Steruliaceae

0.43

0.427

0.204

1.061

85

Cola reticulata

Steruliaceae

0.107

0.107

0.031

0.245

86

Combretodendron macrocarpum

Lecythidaceae

0.107

0.107

0.087

0.301

87

Cordia millenii

Bignoniaceae

0.107

0.107

0.032

0.246

88

Cynometra mannii

Caesalpinaceae

0.215

0.213

0.145

0.573

89

Cynometra megalophylla

Caesalpinaceae

0.107

0.107

0.04

0.254

90

Dacryodes edulis

Burseraceae

1.611

1.601

2.057

5.27

91

Dacryodes klaineana

Burseraceae

0.322

0.32

0.366

1.008

92

Daniellia ogea

Ceasalpinaceae

0.644

0.64

0.56

1.845

93

Dennettia tripetala

Annonaceae

0.215

0.213

0.042

0.47

94

Detarium senegalense

Caesalpinaceae

0.107

0.107

0.154

0.368

95

Dialium dinklagei

Caesalpinaceae

0.107

0.107

0.132

0.346

96

Dialium guineense

Caesalpinaceae

1.611

1.708

1.439

4.758

97

Dichaetanthera Africana

Melastomataceae

0.215

0.213

0.064

0.492

98

Dichapetalum spp

Melastomataceae

0.107

0.107

0.026

0.24

99

Didelotia Africana

Ceasalpinaceae

0.215

0.213

0.165

0.593

100

Diospyros abyssinica

Ebenaceae

0.107

0.107

0.121

0.335

101

Diospyros barteri

Ebenaceae

0.215

0.213

0.052

0.481

102

Diospyros dendo

Ebenaceae

0.43

0.427

0.193

1.05

103

Diospyros mannii

Ebenaceae

0.322

0.32

0.387

1.029

104

Diospyros mespiliformis

Ebenaceae

1.826

1.814

1.137

4.777

105

Diospyros nigerica

Ebenaceae

0.215

0.213

0.109

0.538

106

Diospyros preussi

Ebenaceae

0.322

0.32

0.169

0.811

107

Diospyrus spp

Ebenaceae

0.107

0.107

0.206

0.42

108

Distemonanthus benthamianus

Caesalpinaceae

0.107

0.107

0.025

0.239

109

Dracaena arborea

Dracaenaceae

0.43

0.427

0.283

1.139

110

Drypetes chevalieri

Euphorbiaceae

0.107

0.107

0.144

0.358

111

Ekebergia senegalesis

Meliaceae

0.215

0.213

0.072

0.5

112

Enantia chlorantha

Annonaceae

0.107

0.107

0.031

0.245

113

Entandrophragma angolense

Meliaceae

1.611

1.601

2.604

5.816

114

Entandrophragma cylindricum

Meliaceae

1.719

1.708

2.672

6.098

115

Entandrophragma utile

Meliaceae

0.537

0.534

0.774

1.845

116

Eribroma oblonga

Malvaceae

0.215

0.213

0.082

0.51

117

Eriocoelum macrocarpum

Sapindaceae

0.215

0.213

0.212

0.641

118

Erythrina vogelii

Caesalpinaceae

0.322

0.32

0.257

0.899

119

Erythrophelum suaveolens

Caesalpinaceae

0.107

0.107

0.09

0.304

120

Erythroxylum mannii

Erthroxylaceae

0.215

0.213

0.124

0.552

121

Ficus capensis

Moracaae

0.752

0.747

0.157

1.656

122

Ficus congensis

Moraceae

0.537

0.534

0.149

1.22

123

Ficus exasperate

Moraceae

1.182

1.174

0.431

2.786

124

Ficus mucuso

Moraceae

0.107

0.107

0.014

0.228

125

Ficus vogeliana

Moraceae

0.43

0.427

0.091

0.947

126

Funtumia elastica

Apocynaceae

1.826

1.814

0.789

4.43

127

Garcinia kola

Moraceae

1.074

1.067

0.359

2.501

128

Garcinia livingstonei

Moraceae

0.215

0.213

0.047

0.475

129

Garcinia manii

Apocynaceae

0.859

0.854

0.446

2.16

130

Gilbertiodendron dewevrei

Caesalpinaceae

0.215

0.213

0.18

0.608

131

Gmelina arborea

Verbenaceae

1.182

1.174

1.948

4.303

132

Grewia coriacea

Tillaceae

0.215

0.213

0.077

0.505

133

Guarea glomerulata

Meliaceae

0.43

0.427

0.172

1.028

134

Hannoa klaineana

Simaroubaceae

0.752

0.747

0.474

1.973

135

Harungana madagascariensis

Guttiferae

0.322

0.32

0.182

0.824

136

Heinsia crinata

Myristicaceae

0.107

0.107

0.019

0.233

137

Hevea brasiliensis

Euphorbiaceae

0.537

0.534

0.136

1.207

138

Hexalobus crispiflorus

Annonaceae

0.107

0.107

0.027

0.241

139

Hildegardia barteri

Sterculiaceae

0.107

0.107

0.031

0.245

140

Holarrhena floribunda

Apocynaceae

0.215

0.213

0.066

0.495

141

Holoptelea grandis

Ulmaceae

0.107

0.107

0.019

0.234

142

Homalium lelestui

Salicaceae

0.322

0.32

0.073

0.716

143

Hunteria eburnean

Apocynaceae

0.322

0.32

0.105

0.747

144

Hylodendron gabunense

Caesalpiniaceae

0.43

0.427

0.133

0.99

145

Hymenodictyon biafranum

Myristicaceae

0.215

0.213

0.162

0.591

146

Hymenostegia afzelia

Caesalpinaceae

0.107

0.107

0.213

0.427

147

Irvingia gabonensis

Irvingiaceae

1.504

1.494

2.669

5.667

148

Irvingia grandifolia

Meliaceae

0.107

0.107

0.059

0.273

149

Irvingia wombolu

Irvingiaceae

0.859

0.854

1.32

3.033

150

Khaya grandifoliola

Meliaceae

0.967

0.961

1.142

3.069

151

Khaya ivorensis

Meliaceae

1.933

2.028

2.903

6.865

152

Kigelia Africana

Bignoniaceae

0.107

0.107

0.016

0.23

153

Klainedoxa gabonensis

Irvingiaceae

0.322

0.32

0.873

1.515

154

Lannea welwitschii

Anacardiaceae

0.107

0.107

0.032

0.246

155

Lecaniodiscus cupanioides

Sapindaceae

0.107

0.107

0.02

0.234

156

Leonardoxa Africana

Caesalpiniaceae

0.107

0.107

0.059

0.273

157

Lepidobotrys staudtii

Linaceae

0.215

0.213

0.119

0.547

158

Leptonychia pallid

Sterculiaceae

0.215

0.213

0.041

0.469

159

Lophira alata

Ochnaceae

1.826

1.814

1.657

5.297

160

Lovoa  trichilioides

Meliaceae

1.504

1.601

1.902

5.006

161

Macaranga barteri

Euphorbiaceae

0.107

0.213

0.043

0.364

162

Maesobotrya staudtii

Euphorbiaceae

0.107

0.107

0.032

0.246

163

Magnifera indica

Anacardiaceae

0.215

0.213

0.492

0.92

164

Mallotus oppositifolius

Euphorbiaceae

0.107

0.107

0.026

0.24

165

Mammea Africana

Guttiferae

0.322

0.32

0.224

0.867

166

Mangifera indica

Anacardiaceae

0.43

0.427

0.529

1.385

167

Mansonia altissima

Sterculiaceae

0.107

0.107

0.014

0.228

168

Markhamia tomentosa

Bignomaceae

0.107

0.107

0.105

0.32

169

Massularia  acuminate

Rubiaceae

0.107

0.107

0.044

0.258

170

Microberlinia bisulcata

Caesalpiniaceae

0.215

0.213

0.156

0.584

171

Microdesmis puberula

Pandaceae

0.107

0.107

0.064

0.278

172

Milicia excels

Moraceae

2.256

2.241

4.97

9.467

173

Millettia macrophylla

Papiloniaceae

0.215

0.213

0.075

0.503

174

Mitragyna ledermannii

Rubiaceae

0.107

0.107

0.181

0.396

175

Moringa oleifera

Moringarceae

0.43

0.427

0.705

1.562

176

Morus mesozygia

Moraceae

0.322

0.32

0.211

0.854

177

Musanga cecropioides

Urticaceae

1.182

1.281

2.315

4.778

178

Myrianthus preussii

Cecropiaceae

0.107

0.107

0.027

0.241

179

Napoleonaea vogelii

Lecythidaceae

0.43

0.534

0.278

1.242

180

Nauclea diderrichii

Rubiaceae

1.182

1.174

1.486

3.842

181

Newbouldia laevis

Bignomaceae

0.859

0.854

0.454

2.167

182

Newtonia duparquetiana

Mimosaceae

0.107

0.107

0.04

0.254

183

Octoknema affinis

Olacaceae

0.322

0.32

0.163

0.805

184

Omphalocarpum elatum

Sapotaceae

0.107

0.107

0.023

0.237

185

Oubanguia alata

Scytopetalacea

0.107

0.107

0.042

0.256

186

Oxystigma mannii

Caesalpiniaceae

0.215

0.213

0.167

0.595

187

Parinari chrysophylla

Rubiaceae

0.107

0.107

0.025

0.239

188

Parkia bicolor

Mimosaceae

0.537

0.534

0.487

1.557

189

Paropsia guneensis

Passifloraceae

0.107

0.107

0.021

0.235

190

Pausinystalia talbotiic

Rutaceae

0.107

0.107

0.054

0.268

191

Pentaclethra macrophylla

Mimosaceae

1.504

1.494

1.842

4.839

192

Persea Americana

Lauraceae

0.537

0.534

0.811

1.882

193

Piptadeniastrum africanum

Mimosaceae

1.396

1.387

4.643

7.427

194

Poga oleosa

Rhizophoraceae

0.107

0.107

0.128

0.342

195

Psidium guajava

Myrtaceae

0.215

0.213

0.034

0.462

196

Pterocarpus mildbraedii

Papiloniaceae

0.107

0.107

0.043

0.257

197

Pterocarpus osun

Mimosaceae

0.43

0.427

0.27

1.127

198

Puasinystalia talbotii

Rutaceae

0.107

0.107

0.054

0.268

199

Pycnanthus angolensis

Myristicaceae

0.644

0.64

0.868

2.153

200

Pycnanthus microcephalus

Myristicaceae

0.107

0.107

0.033

0.247

201

Randia longiflora

Rubiaceae

0.43

0.427

0.186

1.043

202

Raphia hookeri

Arecaceae

0.215

0.213

0.109

0.537

203

Rauvolfia vomitoria

Apocynaceae

0.107

0.107

0.087

0.301

204

Rhaptopetalum beguei

Scytopetalaceae

0.107

0.107

0.019

0.234

205

Ricinodendron heudelotii

Euphorbiaceae

0.967

0.961

0.437

2.364

206

Rinorea dentate

Violaceae

0.107

0.107

0.054

0.268

207

Roystonea regia

Palmae

0.107

0.107

0.017

0.231

208

Santiria trimera

Burseraceae

0.107

0.107

0.043

0.258

209

Sapium ellipticum

Euphorbiaceae

0.107

0.107

0.086

0.3

210

Scyphocephalum mannii

Myristicaceae

0.107

0.107

0.105

0.319

211

Spondias mombin

Annacardiaceae

0.752

0.747

0.567

2.066

212

Stemonocoleus micranthus

Papiloniaceae

0.107

0.107

0.017

0.231

213

Strombosia grandifolia

Olacaceae

0.107

0.107

0.021

0.235

214

Strombosia scheffleri

Olacaceae

0.107

0.107

0.129

0.343

215

Tabernaemontana crassa

Apocynaceae

0.107

0.107

0.017

0.231

216

Tabernaemontana pachysiphon

Apocynaceae

0.107

0.107

0.087

0.301

217

Tectona grandis

Verbenaceae

0.322

0.32

0.631

1.274

218

Terminalia ivorensis

Combretaceae

0.859

0.854

0.906

2.619

219

Terminalia superb

Combretaceae

0.537

0.534

0.705

1.776

220

Tetrapleura tetraptera

Mimosaceae

0.752

0.747

0.66

2.159

221

Thecacoris leptobotrya

Euphorbiaceae

0.107

0.107

0.119

0.333

222

Theobroma cacao

Malvaceae

0.322

0.32

0.064

0.706

223

Treculia Africana

Moraceae

1.289

1.281

2.462

5.031

224

Treculia obovoidea

Moraceae

0.215

0.213

0.165

0.594

225

Trema guineensis

Ulmaceae

0.107

0.107

0.02

0.234

226

Trema orientalis

Ulmaceae

0.215

0.213

0.149

0.577

227

Trichilia welwitschii

Meliaceae

0.322

0.32

0.067

0.71

228

Trichillia gilgiana

Meliaceae

0.107

0.107

0.018

0.232

229

Trilepisium madagascariense

Moraceae

0.107

0.107

0.149

0.363

230

Triplochiton scleroxylon

Sterculiaceae

0.322

0.32

0.137

0.779

231

Uapaca acuminata

Euphorbiaceae

0.107

0.107

0.032

0.246

232

Uapaca heudelotii

Euphorbiaceae

0.107

0.107

0.214

0.428

233

Uapaca togoensis

Euphorbiaceae

0.43

0.427

0.311

1.167

234

Uvariastrum elliotianum

Annonaceae

0.107

0.107

0.111

0.326

235

Uvariopsis bakeriana

Annonaceae

0.107

0.107

0.03

0.244

236

Vernonia conferta

Asteraceae

0.43

0.427

0.179

1.036

237

Vitex doniana

Verbenacea

0.537

0.534

0.14

1.211

238

Voacanga africana

Apocynaceae

0.215

0.213

0.067

0.496

239

Xylopia acutiflora

Annonaceae

0.107

0.107

0.017

0.231

240

Xylopia aethiopica

Annonaceae

0.107

0.107

0.137

0.352

241

Xylopia africana

Annonaceae

0.107

0.107

0.032

0.246

242

Xylopia staudtii

Annonaceae

0.107

0.107

0.039

0.253

243

Xylopia talbotii

Annonaceae

0.322

0.32

0.353

0.995

244

Zanthoxylum gilletii

Rutaceae

0.107

0.107

0.015

0.229

245

Zanthoxylum macrophylla

Rutaceae

0.215

0.213

0.314

0.743

246

Zanthoxylum rubescens

Rutaceae

0.107

0.107

0.03

0.244

247

Zanthoxylum zanthoxyloides

Rutaceae

0.107

0.107

0.017

0.231

248

Zenkerella citrine

Leguninosae

0.107

0.107

0.035

0.249

Table 2 Species composition, abundance, and IVI at Okpon river forest reserve CRS, Nigeria
RF, relative frequency; RD, relative density; RDo, rselative dominance; IVI, importance value index

Species diversity in the sampled transect of okpon river forest reserve

The results in Table 3, across tree species diversity in the sampled transects indicate that Transect (T5) had the highest number of individual tree species (145) and had Shannon wiener index of 4.563 with species richness of 106 closely followed by Transect seven (T7) with one hundred and twenty one (121) number of individual species, Shannon wiener index  and species richness of 4.203 and 75 respectively. Transects one and three (T1 and T3) recorded the same number of individual tree species (118); the Shannon-Wiener indices were 4.405 and 4.079, with species richnesses of 88 and 67, respectively. The least number of species, 93, with a Shannon number of 3.925 and a species richness of 57, was recorded in Transects 8 (Table 3). The summary of diversity indices across the sampled transects at the Okpon River Forest Reserve presented in Table 4 shows that the Shannon Weiner index minimum and maximum values were 3.925 and 4.563 with a mean value of 4.287, while species richness had a minimum and maximum of 57 and 106 with an average value of 81.75. Both the Shannon Weiner index and species richness had standard deviations of 0.212 and 15.508, respectively. Table 5 indicates species diversity indices in the study area; Shannon weiner index recorded (5.058), Simpson’s index (0.991), Pielou eveness index (0.917) and Margelef index recorded (36.097). The results of species richness recorded 248 trees in the study sites. Table 5

Transects

Number of

Shannon-Weiner

Species

 

Individuals

Index(HI)

Richness

Transects 1

118

4.079

67

Transects 2

111

4.261

79

Transects 3

118

4.405

88

Transects 4

117

4.432

92

Transects 5

145

4.563

106

Transects 6

114

4.431

90

Transects 7

121

4.203

75

Transects 8

93

3.925

57

Table 3 Species diversity in the sampled transects at Okpon river forest reserve

 Statistic parameters

Shannon-Weiner index

Species richness

Mean

4.287

81.75

Standard deviation

0.212

15.508

Minimum

3.925

57

Max

4.563

106

Number of transects

8

8

Table 4 Summary statistic of diversity indices across the sampled Transects at Okpon river forest reserve

Diversity indices

Index value

Shannon-Weiner index

5.058

Simpson's index

0.991

Pielou evenness index

0.917

Margalef index

36.097

Richness

248

Table 5 Overall species diversity in the study area

Discussion

Forest Structure of Ukpon River Forest Reserve

Diameter and height distributions reflect the horizontal structure and vertical pattern of the forest; these are indications that the forest has the potential for continuous growth. However, the presence of large trees has been reported to be a sign of mature tropical rainforest Zang et al. According to Adekunle et al.,7 222 tree stands were found to be in the lower Dbh class of 10–20 cm, followed by 21–30 cm, which had 78 tree stands, and 72 tree stands in the higher Dbh class of 81 cm. Hence, he reported that the diameter distribution indicated healthy recruitment potentials. The lower-class diameter tree stands could develop into mature trees and replace the old ones in the future if proper conservation efforts are sustained. Thus, this structure is typical of a natural forest.8,9 The minimum and maximum Dbh of trees in the study area were 10.1 m and 80.5 m, respectively. The forest reserve was characterized by an abundance of trees with small Dbh, which is not unusual for tropical rainforests. Similar results have been reported by previous workers in other tropical rainforests in Nigeria.10 The reason for relatively fewer number of individual trees with large Dbh values greater than >0.70 (Dbh>70) could be attributed to forest degradation activities which may have removed large individuals as well as the facts that some large-sized trees would have been removed through logging operation for some uses in the past.11

Tree species diversity and distribution in okpon river forest reserve

The results of this study recorded 68 tree species belonging to 34 families. Caesalpinceae, Moracea and Meliacea   were the most abundance families. The area is rich in terms of tree species composition. However, the number is lower when compared with the 99 tree species belonging to 36 families recorded in the Takamanda Rainforest of Southwest Cameroon.12 Similarly, it is lower than 118 tree species reported by Adeyemi et al.,13 for the Oban Division of the Cross River National Park in Nigeria. A higher number of tree species increases the number of ecological niches for fauna and understory flora. Thus, the presence of numerous tree species on a stand conserves not only more trees but other organisms as well. Comparing the results of this study to a similar study by Oluwatosin et al., in Onigambari forest reserve, Ondo State, Nigeria, they obtained a higher number of families (54) of tree species, while Miazu.14 reported four families in Kuyambana forest reserve, Zamfara State, Nigeria, even lower than the presence study of 34 families recorded in Okpon river forest reserve. He reported the dominance of the Caesalpinaceae, Mimosaceae, and Combretaceae families. This finding corroborated the works of Adekunle (2013), who reported that the tropical rainforest ecosystems of southwest Nigeria are dominated by some specific families such as the Sterculiaceae, Meliaceae, and Moraceae. In this present study, Okpon River Forest Reserve was dominated by the Caesalpiniaceae, Meliaceae, and Moraceae families.

Fabaceae, Melicea, and Caesalpiniacea have been reported as dominant plant families in Nigerian tropical forests.10 The effect of anthropogenic activities on the growth and distribution of tree species may have played a role in the status of these species in the ecosystem, threatening the occurrence and development of certain species while favouring others. The Caesalpinaceae, Meliaceae, Moraeceae, and Euphorbiaceae were the most prevalent families in the study area. This could be due to their fast regeneration ability associated with symbiotic properties, which may have enabled the species to easily establish within different habitat types. Deka et al. (2012) reported that legumes were the most prominent species recorded in Takamanda forest. This may not be far from the fact that the two forest reserves share some ecosystem characteristics and geographic boundaries.

The value of the Shannon Wiener index for tree species in this present study was (5.05). The value recorded in this study is higher than what was reported in other forest reserves; for instance, Parthasarathy (2001) reported H1 3.89, while Adekunle and Olagoke (2010) reported H1 4.02 for rainforest in India and Nigeria, respectively. This result is also in line with the findings of Bhat and kaveriappa (2013) who  obtained among the fresh water swamp forest of kulathupazha, Anchal, Shendumeg, Karthakani, Pilarlarkan and Charmady Karnataka, Shannon wiener of (2.53), (3.69), (2.46), (4.04), (3.25) and (4.90) were recorded respectively. The reason for the high Shannon wiener in this present study could probably be due to the existing management practices, enacted law enforcements programs and anthropogenic activities.

Important value index for tree species

The tree with the highest importance value in the reserve was Brachystegia eurycoma (10.6%) followed by Milicia excelsa (9.4%). This is consistent with the works of Soumana et al., who reported that, most tree species could grow best in loamy sandy soils. The tree with the lowest importance index in the study area was Pterocarpus osun (1.1%). This could likely be due to the multi-purpose usefulness (commercial and medicinal uses) of the tree, which is very important to the local economy. According to Curtis and Mcintosh (1951), a high importance value index IVI of a species indicates its dominance and ecological success, its good power of regeneration, and a greater ecological amplitude; these plants also need conservation management, while species that were grouped as having a low importance value therefore need high conservation effort Abdullahi, Abba. The highest regeneration potentials were recorded in Treculia africana (0.025%), which is quite lower in value than the 0.189% Culcacia saxatilis species obtained in the Onigambari forest reserve in Oyo State, Nigeria, by Salami et al. (2016). The differences in value could be attributed to the management practises adopted in the forest reserve. The regeneration potential in the study area was generally very poor. This has a serious implication on the regeneration and conservation of the various species encountered on the renewal of the forest in general. Wale et al. (2012) also noted that lack of adequate regeneration is an issue recognised by foresters and ecologists. Malik and Bhat (2016) also observed limited regeneration and subsequently declining populations of some dominant native species. Jaya Kumar and Nair (2013) observed in their study that only 101 species regenerate well, with one of the dominant species having no seedlings, which is an indication of poor regeneration.15–21

Conclusion and recommendation

Based on the results of this finding, a total of 68 tree species from 34 families were encountered in the study area. The results indicate that, Meliaceae had the highest number (6) of tree species, Caesalpiniceae had 5 species. There was low tree species density and high species diversity in the study area. The dominant height in the reserve was 40 m, with a Dbh class of 10–20 cm, which tends to dominate. To ensure suitable habitat for sustainable wildlife management and to prevent the extinction of some tree species in the area, there is a need to restrict logging activities and other illegal activities that have a negative effect on stand density and species distribution and abundance. Also, tight control of natural areas should be highly promoted because it is impossible to overstate how much they contribute to preventing climate change in the Ukpon area of Nigeria's Cross River State.

Acknowledgments

None.

Conflicts of interest

Authors declare that there are no conflicts of interest.

References

  1. Sushma S, Subair A, Chandra M, et al. Tree species richness, diversity and regeneration status in different oak (Quercus spp) dominated forest of garhwal himalaya India. Journal of Asia Pacific Biodiversity. 2016;9:293–300.
  2. Malik ZA, Hussan A, Igbal,K. Species Richness and diversity along the distribution gradient in Kadonath Wildlife Sanctuary and its adjourning areas in Garhwal Himalaya, India. International journal of Current Research; 2014.
  3. Neelo JD, Teketay K, Kashe, et al. Stand structure, diversity and regeneration status of woody species in open and ex close dry wood land sites around molapo farming areas of the Okavango delta, Norlheasterm Botswana. Open Journal of Forest. 2015;5 (4):313–228.
  4. Malhi Y, Lewis SL, Mayaux P, et al. African rainforests; past; present and future. Philosophical transactions of the rayal society Biological Science; 2013.
  5. Pushpangadam P. Economic evaluation of biodiversity in context of CBD and IPR regimes. In: regional training programed on biodiversity systematics evaluation and monetary with emphasis on medicinal plants. National Botanical Research Institute: Lucknow India; 2001.
  6. Gillison AN. Biodiversity assessment in the north bank landscape, North East India: a preliminary survey; 2004.
  7. Adekunle VAJ. Olagoke AO, Akindele SO. Tree species diversity and structure of a nigeria strict nature reserve. Tropical Ecology. 2013;54(3):275–289.
  8. Ogana FN, Gorgoso, Varela JJ. Comparison of estimation methods for fitting meibull distribution to the natural stand of oluwa forest reserve, Ondo State, Nigeria. Journal of Research in Forestry. Wildlife and Environment. 2015;7(2):81–90.
  9. Dau JH, Vange T, Amonum JI. Growth space requirements models for Daniellia Oliverii (Rolfe) hutch and Daviz tree in Makurdi, Nigeria. International Journal of Forestry and Horticulture (IJFH). 2016;2(3):31–39.
  10. Adekunle VAJ, Olagoke AO. Diversity and bio volume of tree species in natural forest ecosystem in the bitumen – producing area of Ondo state, Nigeria. Baseline study Biodiversity and Conservation. 2008;17:2735–2755.
  11. Hadi S, Zieglar T, Waltert M, et al. Tree diversity and forest structure in northern Siberut, Mentawai island, Indonesia. Tropical Ecology. 2009;50(2):315–327.
  12. Egbe EA, Chuyong GB, Fonge BA, et al. Forest disturbance at korup national park. Cameroon. International Journal of Biodiversity Conservation. 2012;4(11):377–384.
  13. Adeyemi AA, Jimoh SO, Adesoye PO. Assessment of tree diversities in oban division of the cross river nation park (CRNP), Nigeria. Journal of Agriculture, Forestry and the Social Sciences. 2013;11(1):216–230.
  14. Miazu A. Woody plants genetics resources of kuyambana forest reerve, Mara zamfara state. Dissertation on department of biological sciences, Usman danfodiyo university, Sokoto; 2010.
  15. Abdulahi MB. Phytosociological studies and community rural appraisal towards biodiversity conservation in yankari: Game reserve, Bauchi state, Nigeria. Abubakar Tafawa Belawa University, Bauchi, Nigeria; 2010.
  16. Adekunle VAJ, Olagoke AO, Ogundare LF. Rate of timber production in a tropical rainforest ecosystem of southwest nigeria and its implications on sustainable forest management. Journal of Forestry Research. 2010;21:225–230.
  17. Aigbe HI, Akindele SO, Onyekwelu JC. Tree species diversity and density pattern in afi river forest reserve, Nigeria. International Journal of scientific and Technology Research. 2014;3(10):178.
  18. Dekka J, Tripath PO, Khan LM. High dominance of shorea robusta gaertn in alluvial plain kammp sal forest of Assam, North Eastern. India International Journal of Ecosystem. 2002;2(4):67–73.
  19. Haby VA, Marvin L, Baker, et al. Vegetables growers handbook. 4th edition. Compiled by Joseph GM, Frank JD (Emeritus). Texas A & M University. Horticultural and Forestry Science Building College Station, Texas; 2009.
  20. Lippork D, Beck SG, Renson D, et al. Topography and edge effects are more important than elevation as derives of vegetation patterns in a neotropical montane forest. Journal of Vegetation Science. 25;724–733.
  21. Parthasarathy N. Changes in forest composition and structure in three sites of tropical evergneen forest around sengaltheri, western ghats. Current Science. 2015;80(3):389–393.
Creative Commons Attribution License

©2023 Esor, et al. This is an open access article distributed under the terms of the, which permits unrestricted use, distribution, and build upon your work non-commercially.