Variations in Vegetation and Nutrient Composition in Sal and Eucalyptus Stands: A Case Study of Bhagabatichak Forest Area, West Bengal, India
Corresponding author Email: tksahoo.botany@gmail.com
DOI: http://dx.doi.org/10.12944/CWE.16.3.28
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Sahoo T. K. Variations in Vegetation and Nutrient Composition in Sal and Eucalyptus Stands: A Case Study of Bhagabatichak Forest Area, West Bengal, India. Curr World Environ 2021;16(3). DOI:http://dx.doi.org/10.12944/CWE.16.3.28
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Sahoo T. K. Variations in Vegetation and Nutrient Composition in Sal and Eucalyptus Stands: A Case Study of Bhagabatichak Forest Area, West Bengal, India. Curr World Environ 2021;16(3). Available From:
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Article Publishing History
Received: | 04-08-2021 |
---|---|
Accepted: | 15-12-2021 |
Reviewed by: | Nyong Princely |
Second Review by: | Alex K. George |
Final Approval by: | Dr. C. P. Kumar |
Introduction
Forest represents the largest and most natural plant community. Though, today some woody plant species like Eucalyptus sp., Acacia sp., Dalbergia sp. are planted by human being for their economical need. This type of stands has traditionally been seen as a source of timber1.The return from different non-timber forest products (NTFPs) has been undervalued. But in recent decades, interest has grown in uses of NTFPs as alternatives or supplements of forest products, which are important for economic purpose of the local forest dwellers 2 3 4 5 6. Now-a-days in few forests areas, during afforestation, some fruit yielding species, medicinal plant species are being planted as a policy decision. Plantation of these tree species are done to enhance diversity and heterogeneity in the tree level. Today establishment of new forest has been increased remarkably 7 8 9. Since 1990 in India, as well as in West Bengal a major portion of the natural coppice sal forest is protected by concerned Forest Protection Committee (FPC) through Joint Forest Management (JFM), which was previously in a degraded condition and maintained by the State Forest Department10.There are the great differences of natural forest from a plantation ecosystem regarding the vegetation dynamics, structure and function also11. The quality and quantity of undergrowth depends on the tree canopy and the edaphic and microclimatic conditions existing under the particular type of forest12. The nature of ground flora, its diversity and density vary with the type of forest community13. The proportion of species to genera were 13:1 in world, 7:1 in India and 1.5:1 in Amarkantak, Madhya Pradesh, India14. It indicates that every genus is of great botanical importance in any plant community. The species diversity, density and nature of vegetation vary with the type of forest15.
In this study the vegetation and nutrient composition of a sal dominated stand (natural forest) was compared with that of eucalyptus stand (plantation) in Paschim Midnapore district. The forest of Paschim Midnapore district is truly unique, which shows higher species diversity16, 17. As per Champion and Seth’s classification of Forest Type of India, the study area comes under Major Group – II, i.e. “Dry Tropical Forest”18.
Study Area
The study was done in Bhagabatichak forest area under Midnapore East Forest Division, West Bengal. This area has two type of stands, such as coppice sal stand (CSS) and coppice eucalyptus stand (CES), which are adjacent to each other. Sal stand was jointly managed by FPC and Forest Department, whereas eucalyptus stand was under management of Forest Department. In CES eucalyptus plantation was done by Forest Department. Bhagabatichak village is 8 km away from Midnapore town of Paschim-Midnapore District, where FPC has existed for the last 25 years. The area of the coppice sal (Shorea robusta) stand is 61 hectares and the area of the eucalyptus stand is 33 hectares. Bhagabatichak forest belongs to the latitude 22.46140N and longitude 87.27800E. The annual rainfall of this site is 1580 mm of which 80% is precipitated at the end of June to September. The mean minimum and maximum temperature ranges from 15.6oC to 37.8oC.
Material and Methods
The phyto-sociological observations in both stands were recorded every month during 2019 -20 using quadrat method15. The data were represented in pre-monsoon, monsoon and post-monsoon seasons. Pre-monsoon represents March to June, monsoon July to October and post-monsoon November to February.
Layout of Sample Plots
“Species area curve” method was used to determine the minimum size and minimum number of the quadrats19. To study the plant communities quadrats of (10 m X 10 m) for tree species, (5m X 5m) for shrubs and (1m X 1m) for herbs were selected randomly. Ten quadrats of each (tree, shrub and herb) were studied in both the stands. Quadrat wise plant species were encountered, listed and then identified with the help of floristic study of regional vegetation by Prain20.The identifications were cross checked with the help of Bennet21. Different phytosociological parameters were measured as follows-
Importance Value Index (IVI) – IVI = RD+RA+RF22
Where, RD= Relative Density, RA= Relative Abundance and RF= Relative Frequency.
Diversity Index (H/) =
where, ni = IVI of individual species and N= IVI of all the species.
The concentration of Dominance (Cd)
It was measured by Simpson’s Index24, Cd = (ni /N) 2, where, ni = IVI of individual species and N= IVI of all the species
Species Richness Index (d) - d = S -1 / log N25, where, S= Total number of species, N= IVI of all the species.
Beta Diversity ( βd ) - βd = Sc/ S 26, where, Sc = total number of species in all the sites and S = average species per site.
Similarity (IS) or Quotient of Similarity (QS) –
This was calculated by the formula of Sorensen27, which was described by Muller-Dombois and Ellenberg28. IS or QS = 2c / a + b, Where, a = Total number of plant species in one stand, b = Total number of plant species in another stand, c = Total number of plant species in both the stand.
Biomass
The above ground biomass were collected by destructive method. Destructive sampling of different species was done thrice (pre-monsoon, monsoon and post-monsoon). Species wise dry biomass estimated after drying the sample in Hot air oven at 800c for 24 hours.
Nutrient Composition
For assessing composition of flora, the plants from all the quadrats were harvested, identified and sorted out into dominant, co-dominant and other associated species by their occurrence/frequency in the forest. The vegetation was weighed, chopped, dried at 60oC, re-weighed, grind to fine power and analyzed for nitrogen, phosphorus, and potash29.
Soil pH
The pH meter is used to measure the soil pH, with the help of glass electrodes in 1: 1.25 of soil: water.
Result and Discussion
In a place the plant community nature is depend upon the plant species which grow and develop in this environment30. The variation of community composition between the two adjacent coppice stands and the effect of dominant tree species on other species were studied. The study reveals that more plant species were present in coppice sal stand (CSS) than coppice eucalyptus stand (CES). The numbers of tree and shrubs species were more or less the same in all three seasons in both the study sites (Table-1), but in case of herbs many species regenerate during monsoon period, which are not available in other seasons (Table-1). Maximum numbers of plant species were available in monsoon period, 71 in CSS, among them15 tree species, 22 shrubs and climbers, 34 herbs and grasses. Whereas during monsoon period the total number of plant species in CES were only 43, among them 11 tree species, 13 shrubs and climbers, 19 herbs and grasses (Table-1). Similar observations were recorded in natural coppice sal forest and akashmoni (Acacia auriculiformis A. Cunn. Ex. Benth. Ln. Hook.) plantation stand of Paschim-Minapore district of West Bengal31. Several authors were noted that the variations of vegetation are depends upon several factors like species composition and structure32, management strategies33, soil moisture and nutrient dynamics34, 35, succession history36 and fragmentation37. Occurrence of maximum number of plant species (71) in CSS shows its status as climatic climax, besides this, the stand is protected by FPC, so the disturbances were least. In CES the total number of species (43) was too much less than CSS during monsoon period, where the different disturbances like thinning, pruning, cutting, collection of fuel wood, grazing are too much high, so the number of species is too much less.
Table 1: Number of Plant Species in CSS and CES.
|
Coppice Sal Stand (CSS) |
Coppice Eucalyptus Stand (CES) |
||||
|
Pre -monsoon |
Monsoon |
Post -monsoon |
Pre-monsoon |
Monsoon |
Post -monsoon |
Tree species |
15 |
15 |
15 |
9 |
11 |
10 |
Shrubs & climbers |
17 |
22 |
22 |
10 |
13 |
11 |
Herbs & grasses |
16 |
34 |
30 |
12 |
19 |
15 |
TOTAL |
48 |
71 |
67 |
31 |
43 |
36 |
IVI of a plant community represents the ecological importance of a species in the community. In CSS highest IVI was occupied by sal in all the seasons (Table- 2), during monsoon this was followed by Croton roxburghii (14.53), then Combretum roxburghii (14.16). Similarly in CES highest IVI was occupied by eucalyptus in all the seasons (Table- 2), during monsoon E. tereticornis was followed by Lantana camara (14.23) and Combretum roxburghii (13.17) which are listed in Table-2. The result also shows that in between the sal and eucalyptus maximum IVI was occupied by eucalyptus in CES than the sal in CSS. It indicates the effectiveness of major species on other species was more by eucalyptus than sal. On the basis of the “Kath and Kukath” concept the FPC protects the forest specially the sal tree. But recent days different NTFPs are used and sold in the market, which support the economy of the forest people. So they protect the forest as a whole, which promote the conservation of forest. Similar findings were observed by some authors2, 6. The village people irregularly collect the different tree species (except sal) as fuel wood. These tree species remain in sapling condition throughout the year. Another dominant species like, Combretum roxburghii, Holarrhena antidysenterica and L. camara remain constant and showed better growth in CSS. Whereas in CES the grazing and cutting of different plant species (except eucalyptus) were done continuously, no restrictions were there. Though in CES Combretum roxburghii, C. viscosum, L. camara, constantly present but not in better condition as in CSS.
Table 2: Importance Value Index (IVI) and Annual Above Ground Biomass of all the Species in CSS and CES.
|
|
Coppice Sal Stand (CSS) |
Coppice Eucalyptus Stand (CES) |
||||||
Sl. No |
Scientific name |
IVI |
Annual Above Ground Biomass (kg/ha/yr) |
IVI |
Annual Above Ground Biomass (kg/ha/yr) |
||||
Pre -monsoon |
Monsoon |
Post -monsoon |
Pre -monsoon |
Monsoon |
Post -monsoon |
||||
|
TREE species |
|
|
|
|
|
|
|
|
01 |
Acacia auriculiformis A. Cunn. Ex.Benth. Ln. Hook. |
x |
x |
x |
x |
6.12 |
5.39 |
5.88 |
50.514 |
02 |
Alstonia scholaris R.Br. |
8.47 |
8.33 |
8.41 |
42.647 |
9.15 |
7.91 |
8.48 |
28.172 |
03 |
Antidesma acidum Retz. |
8.81 |
8.74 |
8.69 |
182.203 |
x |
2.27 |
x |
15.218 |
04 |
Buchanania lanzan Spr. |
11.23 |
10.67 |
9.41 |
105.732 |
x |
x |
x |
x |
05 |
Cassia fistula Linn. |
13.65 |
12.72 |
12.48 |
243.174 |
x |
x |
x |
x |
06 |
Cleistanthus collinus Benth. |
3.17 |
2.46 |
2.52 |
28.46 |
9.16 |
7.56 |
6.72 |
79.850 |
07 |
Croton roxburghii Balak. |
15.42 |
14.53 |
15.05 |
396.244 |
8.15 |
5.94 |
6.33 |
94.416 |
08 |
Diospyros exculpta Buch-Ham. |
10.94 |
10.87 |
10.58 |
183.752 |
9.69 |
9.80 |
9.93 |
88.623 |
09 |
Eucalyptus tereticornis Sm. |
x |
x |
x |
x |
97.58 |
88.62 |
93.24 |
84246.358 |
10 |
Madhuca longifolia (Koenig) MacBride. |
13.72 |
12.23 |
12.19 |
226.283 |
x |
6.16 |
7.57 |
89.107 |
11 |
Phoenix sylvestris Roxb. |
7.81 |
7.79 |
7.74 |
37.965 |
10.48 |
8.62 |
9.06 |
32.432 |
12 |
Pterocarpus marsupium Roxb. |
5.79 |
5.63 |
5.62 |
32.492 |
x |
x |
x |
x |
13 |
Shorea robusta Gaertn. F. |
47.24 |
42.76 |
44.79 |
82357.946 |
x |
x |
x |
x |
14 |
Sizygium cumini (Linn.)Skeels. |
5.26 |
4.49 |
4.45 |
24.124 |
7.54 |
5.25 |
5.69 |
55.176 |
15 |
Tectona grandis Linn. f. |
12.44 |
11.91 |
11.84 |
145.377 |
x |
x |
x |
x |
16 |
Terminalia bellerica (Gaertn.) Roxb. |
9.27 |
8.73 |
8.79 |
87.852 |
x |
x |
x |
x |
17 |
Zizyphus mauritiana Lamk. |
7.83 |
7.61 |
7.64 |
78.344 |
6.73 |
5.84 |
5.13 |
32.318 |
|
TOTAL ANNUAL BIOMASS |
|
|
|
84172.595 |
|
|
|
84812.184 |
|
TOTAL ANNUAL BIOMASS |
|
|
|
1814.649 |
|
|
|
565.826 |
|
SHRUBS and CLIMBERS |
|
|
|
|
|
|
|
|
01 |
Abrus precatorius Linn. |
2.19 |
1.27 |
1.25 |
2.349 |
x |
x |
x |
x |
02 |
Abutilon indicum(L) Sweet. |
x |
2.45 |
2.87 |
6.805 |
x |
x |
x |
x |
03 |
Allophyllus cobbe (L) Raeusch. |
x |
x |
x |
|
x |
2.91 |
x |
8.361 |
04 |
Butea superba. Roxb. |
4.52 |
3.21 |
3.43 |
14.692 |
6.94 |
6.37 |
6.88 |
12.332 |
05 |
Clerodendrum viscosum Vent. |
6.22 |
4.70 |
4.82 |
78.624 |
12.72 |
11.43 |
12.44 |
356.938 |
06 |
Coccinia indicaNaud. |
x |
2.61 |
2.65 |
12.435 |
x |
x |
x |
x |
07 |
Combretum roxburghii Spreng. |
15.78 |
14.16 |
14.46 |
1832.613 |
13.99 |
13.17 |
13.89 |
427.236 |
08 |
Dioscoria alata L. |
x |
3.16 |
3.63 |
12.864 |
x |
x |
x |
x |
09 |
D. bulbifera L. |
x |
2.84 |
3.10 |
11.962 |
x |
x |
x |
x |
10 |
Flacourtia indica(Burn. f.) Merr. |
2.43 |
2.29 |
1.98 |
14.787 |
9.81 |
8.72 |
9.86 |
28.378 |
11 |
Flamingia chappar Ham. |
2.81 |
1.78 |
1.76 |
3.125 |
x |
x |
x |
x |
12 |
Gardenia gummifera Linn. f. |
2.66 |
2.33 |
2.59 |
4.266 |
x |
x |
x |
x |
13 |
Grewia asiatica L. |
2.32 |
1.42 |
1.67 |
2.350 |
7.46 |
6.94 |
7.70 |
10.329 |
14 |
Hemidesmus indicusR. Br. |
3.58 |
2.14 |
1.78 |
12.763 |
x |
x |
x |
x |
15 |
Holarrhena antidysenterica Wall. |
9.80 |
8.77 |
9.22 |
343.542 |
11.87 |
10.76 |
11.35 |
151.944 |
16 |
Ichnocarpus frutescence R. Br |
3.36 |
2.03 |
2.12 |
3.674 |
x |
x |
x |
x |
17 |
Kirganelia reticulata (Poir.)Baill. |
x |
x |
x |
x |
x |
3.83 |
x |
4.167 |
18 |
Lantana camara L. |
11.48 |
10.24 |
10.81 |
385.765 |
14.94 |
14.23 |
14.46 |
433.036 |
19 |
Mucuna pruriens (L) Dc. |
2.26 |
1.17 |
1.02 |
2.763 |
x |
x |
x |
x |
20 |
Smilax ovalifolia Roxb. |
2.35 |
1.22 |
1.45 |
2.284 |
x |
x |
x |
x |
21 |
Tephrosia purpuria (L) Pers. |
1.82 |
1.78 |
1.73 |
3.174 |
x |
4.82 |
4.54 |
2.164 |
22 |
Tragia hispida Willd. |
x |
x |
x |
x |
4.59 |
3.57 |
4.15 |
|
23 |
Triumfetta rhomboidea Jacq. |
x |
1.66 |
1.68 |
2.846 |
x |
x |
x |
x |
24 |
Vitex negundo Linn. |
2.16 |
1.32 |
1.46 |
3.172 |
6.93 |
6.33 |
6.58 |
15.297 |
25 |
Zizyphus oenoplia Mill. |
2.94 |
2.81 |
3.24 |
41.294 |
4.85 |
4.61 |
4.97 |
34.182 |
TOTAL BIOMASS of SHRUBS & CLIMBERS |
- |
- |
- |
2798.149 |
- |
- |
- |
1484.364 |
|
|
HERBS and GRASSES |
|
|
|
|
|
|
|
|
01 |
Aerva lanata (L) Juss. |
1.41 |
1.32 |
1.15 |
0.535 |
x |
x |
x |
x |
02 |
Ageratum conyzoides Linn. |
2.29 |
1.97 |
2.20 |
0.793 |
x |
x |
x |
x |
03 |
Alysicarpus vaginalis (L) Dc. |
x |
2.17 |
2.18 |
0.678 |
x |
1.49 |
x |
0.870 |
04 |
Andrographis paniculata Nees. |
x |
1.40 |
x |
6.352 |
x |
x |
x |
x |
05 |
Aristida adscensionis L. |
4.26 |
3.82 |
3.96 |
2.793 |
5.37 |
4.45 |
4.28 |
1.327 |
06 |
Atylosia conyzoides Linn. |
x |
1.71 |
x |
0.874 |
x |
x |
x |
x |
07 |
Barleria cristata Linn. |
2.43 |
1.68 |
1.64 |
1.377 |
x |
x |
x |
x |
08 |
Blumea lacera Dc. |
x |
2.14 |
2.34 |
2.884 |
3.67 |
2.78 |
2.94 |
1.379 |
09 |
Borreria articularis (L.f.) F. N. Will. |
x |
1.65 |
1.49 |
0.634 |
x |
x |
x |
x |
10 |
Chrysopogon aciculatus Retz. |
3.85 |
3.37 |
3.28 |
1.324 |
4.91 |
5.97 |
5.58 |
0.878 |
11 |
Cynodon dactylon Pers. |
3.79 |
2.76 |
3.17 |
1.420 |
3.86 |
3.48 |
3.55 |
0.933 |
12 |
Cyperus compresus Linn. |
x |
1.13 |
1.16 |
1.128 |
x |
1.73 |
2.18 |
0.634 |
13 |
C. cyperoides (L) Kuntze. |
x |
0.96 |
1.13 |
0.873 |
x |
x |
x |
x |
14 |
C. rotundus Linn. |
x |
1.47 |
1.56 |
0.947 |
x |
1.28 |
1.42 |
0.537 |
15 |
Desmodium triflorum Dc. |
x |
1.35 |
1.41 |
0.677 |
1.91 |
1.44 |
2.17 |
0.448 |
16 |
Eragrostis tenella Roem&Schtt. |
x |
2.17 |
2.40 |
0.785 |
x |
1.28 |
x |
0.326 |
17 |
Euphorbia hirta Linn. |
2.48 |
1.84 |
1.92 |
0.642 |
x |
x |
x |
x |
18 |
Evolvulus nummularius Linn. |
x |
1.56 |
1.42 |
0.438 |
1.94 |
1.76 |
1.87 |
0.295 |
19 |
Fimbristyles dichotoma (L.) Vahl. |
x |
x |
x |
x |
x |
2.17 |
x |
0.237 |
20 |
F. ovata (Burm.f.) Kern. |
x |
0.87 |
x |
0.244 |
x |
1.18 |
x |
0.138 |
21 |
Hedyotis corymbosa (L) Lamk. |
x |
1.53 |
1.10 |
0.445 |
1.61 |
1.08 |
1.28 |
0.296 |
22 |
Heteropogon contortus (L) Beavu.ex. Roem&Schtt. |
2.73 |
2.16 |
2.14 |
0.783 |
3.49 |
3.73 |
3.86 |
0.323 |
23 |
Lindernia ciliata (Colsm.) Pennell. |
x |
0.76 |
x |
0.186 |
x |
x |
x |
x |
24 |
L. crustacea (L) F. Muell. |
x |
0.87 |
0.95 |
0.214 |
x |
x |
x |
x |
25 |
Mimosa pudica Linn. |
0.72 |
1.34 |
1.28 |
2.832 |
3.14 |
2.35 |
2.44 |
1.488 |
26 |
Mollugo pentaphylla L. |
x |
1.81 |
1.13 |
0.390 |
x |
x |
x |
x |
27 |
Pergularia daemia (Forssk.) Chiov. |
2.80 |
1.45 |
1.48 |
1.427 |
4.37 |
3.68 |
4.72 |
0.836 |
28 |
Perotis latifolia Ait. |
x |
0.67 |
0.73 |
0.226 |
x |
x |
x |
x |
29 |
Phyllanthus fraternus Webstern. |
x |
0.92 |
1.16 |
0.367 |
x |
x |
x |
x |
30 |
Rungia pectinata (L) Nees. |
2.57 |
1.17 |
1.14 |
0.626 |
x |
1.39 |
1.84 |
0.438 |
31 |
Sida cordata (Burn. f.) Borssum. |
2.88 |
2.08 |
2.04 |
0.973 |
x |
x |
x |
x |
32 |
S. rhomboidea Linn. |
2.15 |
1.75 |
1.79 |
0.884 |
3.41 |
3.83 |
3.17 |
1.212 |
33 |
Solanum nigram Linn. |
2.64 |
1.14 |
1.12 |
0.927 |
x |
x |
x |
x |
34 |
Tridax procumbens Linn. |
1.75 |
1.35 |
1.37 |
0.876 |
3.62 |
3.88 |
3.85 |
0.694 |
35 |
Vernonia cinerae (L) Less. |
1.52 |
0.83 |
1.24 |
0.745 |
x |
x |
x |
x |
TOTAL BIOMASS of HERBS & GRASSES |
- |
- |
- |
37.299 |
- |
- |
- |
13.289 |
|
GRAND TOTAL |
300.00 |
300.00 |
300.00 |
87008.043 |
300.00 |
300.00 |
300.00 |
86309.837 |
Vegetation analysis and distribution patterns of this study are as follows, the diversity index (H/) and concentration of dominance (Cd) were calculated on the basis of density and IVI. The information of species richness, distribution and the rate of change in species composition were available from diversity index. The ecosystem process is controlled by the strong function of the structure and diversity of vegetation. Diversity index is an important attribute of an organized community38. The diversity index (H/) was maximum in CSS during monsoon (1.983) and minimum in CES during pre-monsoon (1.228). It indicates that more species were observed in CSS (Table-2). In case of herbs the open canopy indicates the species richness and composition of an ecosystem39. The study reveals that higher species richness values (d) were observed in CSS during all the seasons, among them, the highest was in monsoon (28.259).The lower species richness value were observed in CES throughout the year, among them lowest in pre-monsoon (12.112).In Chendra teak forest of Dhaurpur range in Sarguja district, Chhattisgarh, India, the Shannon diversity index value and species richness value for shrubs of a natural forest was double than the plantation sites of teak11. The values of concentration of dominance (Cd) i.e. dominance index were maximum in CES and minimum in CSS in all the seasons, which are shown in Table- 3. Eucalyptus is a quick growing, large woody, gigantic tree species and the coppicing power is high, so the ecological success of the associated species was found to be very low in terms of their competing ability and therefore the ground vegetation was also found to be very thin. The adaptability and the coppicing ability of eucalyptus are better in lateritic region, a common soil type of the study region40. But sal is a slow growing species and it has no harmful effect on another plant species. The plant diversity was higher in CSS, this was also supported by several authors41, 42.
Table 3: Different Phytosociological Parameters of CSS and CES.
|
Coppice Sal Stand (CSS) |
Coppice Eucalyptus Stand (CES) |
||||
Pre- |
Monsoon |
Post- |
Pre- |
Monsoon |
Post- |
|
Total no. of species |
48 |
71 |
67 |
31 |
43 |
36 |
Diversity Index(H/) |
1.488 |
1.983 |
1.723 |
1.228 |
1.327 |
1.274 |
Dominance Index (Cd) |
0.048 |
0.042 |
0.044 |
0.125 |
0.106 |
0.113 |
Species Richness Index (d) |
18.974 |
28.259 |
26.645 |
12.112 |
16.956 |
14.129 |
β Diversity |
1.215 |
1.245 |
1.300 |
0.784 |
0.754 |
0.699 |
Similarity Index (During monsoon) |
64.91% |
β diversity reflects the rate of species change in the plant communities. It was more in CSS and less in CES, shown in Table-3. It shows highest stability in CSS in comparison to CES. Some authors has quoted that diversity generates community stability, dominance generates community productivity and increasing the number of species in a forest stand rather enhancing efficiency though more exploitation of site resources decreases efficiency perhaps through competition43,44. Greater diversity provides a number of pathways in the ecosystem’s functioning which gives stability to the ecosystem.
The similarity index (IS) is 64.51%, because CSS and CES are situated side by side at the same locality. Though these two stands are situated side by side, but the vegetation was different, due to the effect of dominant species on other species, such as in CSS sal shares the competition with other species but in CES, eucalyptus suppresses the other species45. Due to the different effectiveness of dominant species on other plant species the similarity of these two stands was not higher.
Comparative study of annual above ground biomass (agb) of the two stands shows that the total annual agb was slightly higher in CSS (87008.043 kg ha-1yr-1) than CES (86309.837 kg ha-1yr-1). The difference of agb was (87008.043 – 86309.837) 698.206 kg ha-1 yr-1. But in tree species the individual agb was more in eucalyptus (84246.358 kg ha-1yr-1) than sal (82357.946 kg ha-1yr-1). This is due to the fact that eucalyptus is a fast growing species than sal. In CSS the total agb (except sal) was 4650.07 kg ha-1yr-1. Similar finding was recorded by Sahoo46. Sahoo enumerated the total agb (except sal) in Chandra natural coppice sal forest of Midnapur East Forest Division in West Bengal was 5932.01 kg ha-1yr-1which was quite less in respect of the total annual agb. In CSS the total agb was 87008.043 kg ha-1yr-1, among this, tree species (except sal) contributed only 2.08% (1814.649 kg ha-1yr-1), shrubs and climbers 3.21% (2798.122kg ha-1yr-1), herbs and grasses 0.04% (37.299 kg ha-1yr-1). The rest amount 94.67% (82357.946 kg ha-1yr-1) was contributed by sal only, because sal is the most dominant tree species in this stand, besides this sal is protected by FPC. In CES the total agb was 86309.837 kg ha-1yr-1, among this, tree species (except eucalyptus) has only 0.65% (565.826 kg ha-1yr-1), shrubs and climbers 1.72% (1484.364 kg ha-1yr-1), herbs and grasses 0.02% (13.289 kg ha-1yr-1) and only eucalyptus contribute 97.61% (84246.358 kg ha-1yr-1). Eucalyptus was the dominant tree species in CES. The result shows that the individual agb was more in eucalyptus than sal. With respect to total annual agb, species diversity and stability, the CSS was performed better, more significant and more stable than CES. In CES eucalyptus suppress the growth of other species and allelo-chemicals secreted by eucalyptus which prevents the germination and growth of other species. Similar findings were observed by several authors47, 45.
Nutrient Composition of Major Species
The major species having higher IVI and common to both the stands were selected for performing nutrient composition analysis, which are listed in Table-4. Their respective contribution towards production of biomass and nutrient uptake revealed that in both the stands higher nutrients (available NPK) were observed in Combretum roxburghii. In CSS available NPK were 1.272%, 0.527% and 1.867%. In CES the available NPK values were 0.864%, 0.513% and 1.724% in the same species. Next to Combretum roxburghii more nutrients were observed in L. camara (Table-4). In L. camara more nutrients (available NPK) were observed in CSS than the CES. A similar trend was observed for other species (Table-4). Nutrient uptake efficiency was more in the species of CSS, though sal had optimum expression on these sites. Available NPK were less in the species of CES, these are due to the fact that this stand is open to biotic interference by the local people and considerable amount of understory vegetation is being removed by villagers leading to sparse understory11.
Table 4: Analytical Composition of Major Plants of CSS and CES.
|
|
Analytical Composition of Above Ground Biomass |
|||||
|
|
Coppice Sal Stand (CSS) |
Coppice Eucalyptus Stand (CES) |
||||
Sl. No. |
Scientific Name |
Av. N |
Av. P |
Av. K |
Av. N |
Av. P |
Av. K |
|
Tree / Sapling |
|
|
|
|
|
|
01 |
Madhuca longifolia |
0.761 |
0.394 |
1.324 |
0.685 |
0.317 |
1.278 |
02 |
Croton roxburghii |
0.747 |
0.438 |
1.762 |
0.597 |
0.358 |
1.159 |
|
Shrubs and climbers |
|
|
|
|
|
|
03 |
Clerodendrumviscosum |
0.874 |
0.418 |
1.473 |
0.783 |
0.412 |
1.382 |
04 |
Combretum roxburghii |
1.272 |
0.527 |
1.867 |
0.864 |
0.513 |
1.724 |
05 |
Holarrhenaantidysenterica |
0.856 |
0.422 |
1.383 |
0.628 |
0.329 |
1.247 |
06 |
Lantana camara |
0.879 |
0.515 |
1.642 |
0.835 |
0.487 |
1.686 |
|
Herbs and grasses |
|
|
|
|
|
|
07 |
Alysicarpusvaginalis |
0.873 |
0.313 |
1.217 |
0.768 |
0.280 |
0.936 |
08 |
Aristida adscensionis |
0.792 |
0.349 |
0.946 |
0.728 |
0.311 |
0.876 |
09 |
Chrysopogonaciculatus |
0.637 |
0.288 |
0.917 |
0.624 |
0.228 |
0.836 |
Table 5: Soil pH of CSS and CES.
|
|
1 |
2 |
3 |
4 |
5 |
Mean |
Coppice Sal Stand (CSS) |
Top Soil (0-15)cm |
5.12 |
5.73 |
5.48 |
5.67 |
5.65 |
5.53 |
Sub Soil (15-30)cm |
5.54 |
5.92 |
5.82 |
5.81 |
5.88 |
5.79 |
|
Coppice Eucalyptus Stand (CES) |
Top Soil (0-15)cm |
5.06 |
4.87 |
4.68 |
5.12 |
4.70 |
4.88 |
Sub Soil (15-30)cm |
5.18 |
4.90 |
4.83 |
5.38 |
4.84 |
5.02 |
Mean pH value of soil in CSS was 5.53 in top soil (0 – 15cm.) and 5.79 in subsoil (15 – 30 cm.). The corresponding mean pH value of soil in CES was 4.88 in top soil and 5.02 in subsoil. In the lateritic region of West Bengal the soil pH under coppice sal forest ranges from 5.0 to 6.6, which are acidic to nearly neutral in reaction48. Under neutral pH conditions, rapid transformation, low fixation and efficient extraction of available phosphorus in sal forest soil is more than eucalyptus forest soils49.
Conclusion
The results indicate that the availability and growth of the floral diversity in CSS is more than that of CES. There may be various factors to explain but most important one is the management of the stands. Most of the ecological factors like soil, water regime etc. being same, the dominant tree species of the stands are observed to be the drivers of community structure. Thus, it may be concluded that the sal stand is more stable as compared to the eucalyptus stand. These observations get credence from the fact that sal stand are more stable having better floral composition than the floral composition of eucalyptus stand, which can provide better welfare to human beings and more significant to human life.
Acknowledgment
I am grateful to Dr. S. K. Banerjee, DSc. Senior Scientist (Retd.), TFRI, Jabalpur, MP and Dr. T.K. Mishra, Principal (Retd.), Vidyasagar College, Kolkata, West Bengal, for their guidance and encouragement in this research work. Thanks to all the villagers of Bhagabatichak, those who helped in different ways during the fieldwork.
Funding Source
There is no funding or financial support for this research work.
Conflict of Interest
There is no conflict of interest in the manuscript.
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