3.1 Floristic Composition in Gama Luma
The study aimed to quantify terrestrial biomass accumulation and carbon stock in the ecotone region of Gama Luma, Punakha District. A total of 351 trees from 16 families and 22 species were analyzed, with Myrsinaceae and Pinaceae being the most common families. Trees with a DBH of less than 10 cm were excluded. Myrsine capitellata was the dominant species according to the Important Value Index (IVI) of 67.689, followed by Pinus roxburghii at 37.151, while Zanthoxylum armatum was the least dominant at 1.275 (refer Table 1). Fagaceae had the most species (four), followed by Pentaphylacaceae, Pinaceae, and Rosaceae, which had two species each, and the remaining families had one species each.
Table 1: Floristic composition of the study area in Gama Luma
Tree species
|
ABA (cm2/ha)
|
Relative dominance
|
Relative density
|
Relative frequency
|
IVI
|
Ranks
|
Bc
|
10.101
|
3.938
|
3.419
|
4.386
|
11.743
|
9
|
Bj
|
19.635
|
0.638
|
0.285
|
0.877
|
1.800
|
17
|
Cs
|
3.170
|
0.206
|
0.570
|
0.877
|
1.653
|
19
|
Ct
|
14.801
|
11.541
|
6.838
|
7.018
|
25.396
|
6
|
Ds
|
3.528
|
0.115
|
0.285
|
0.877
|
1.277
|
21
|
Di
|
3.646
|
0.237
|
0.570
|
0.877
|
1.684
|
18
|
Ea
|
6.961
|
1.357
|
1.709
|
3.509
|
6.575
|
11
|
Ec
|
14.037
|
1.368
|
0.855
|
1.754
|
3.977
|
12
|
Ep
|
3.047
|
0.198
|
0.570
|
1.754
|
2.522
|
16
|
Mc
|
4.201
|
16.242
|
33.903
|
17.544
|
67.689
|
1
|
Pr
|
12.671
|
17.290
|
11.966
|
7.895
|
37.151
|
2
|
Pw
|
9.021
|
0.293
|
0.285
|
0.877
|
1.455
|
20
|
Pc
|
34.226
|
2.224
|
0.570
|
0.877
|
3.671
|
13
|
Qg
|
12.060
|
5.485
|
3.989
|
6.140
|
15.614
|
7
|
Qgr
|
14.243
|
12.956
|
7.977
|
12.281
|
33.214
|
3
|
Ql
|
15.642
|
12.197
|
6.838
|
7.895
|
26.929
|
5
|
Ra
|
5.390
|
7.004
|
11.396
|
8.772
|
27.172
|
4
|
Sw
|
8.235
|
3.745
|
3.989
|
5.263
|
12.997
|
8
|
Sp
|
4.859
|
0.316
|
0.570
|
1.754
|
2.640
|
15
|
Sc
|
19.635
|
1.276
|
0.570
|
1.754
|
3.600
|
14
|
Za
|
3.462
|
0.112
|
0.285
|
0.877
|
1.275
|
22
|
Zi
|
4.315
|
1.262
|
2.564
|
6.140
|
9.966
|
10
|
Total
|
226.886
|
100.000
|
100.000
|
100.000
|
300.000
|
|
Abbreviations: ABA- Average Basal Area, IVI- Important Value Index, Bc- Benthamidia capitata, Bj- Bischovia javanica, Cs- Carpinus spp, Ds- Dalbergia sericea, Di- Docynia indica, Ea- Eurya acumionata, Ec- Eurya cerasifolia, Ep- Exbucklandia populnea, Mc- Myrsine capitellata, Pr- Pinus roxburghii, Pw- Pinus wallichiana, Pc- Pyracantha crenulate, Qg- Quercus glauca, Qgr- Quercus graffithii, Ql- Quercus lanata, Ra- Rhododendron arboretum, Sw- Schima wallichii, Sp- Symplocos paniculate, Sc- Syzigium cumini, Za- Zanthoxylum armatum, Zi- Ziziphus incurve
3.2 Species-wise total biomass and carbon stock comparison
The study in the ecotone region of Gama Luma recorded a total of twenty-two tree species with a combined biomass of 7.890 Mg/ha, converting to a carbon stock of 3.945 Mg C/ha (ref. Table 2). Castanopsis tribuloides was the dominant species with a biomass of 1.690 Mg/ha and a carbon content of 0.845 Mg C/ha, while Zanthoxylum armatum had the lowest biomass and carbon sequestration potential at 0.004 Mg/ha and 0.002 Mg C/ha, respectively (ref. Table 2). This analysis highlights the significant contribution of Castanopsis tribuloides to carbon storage, providing valuable insights into the relationship between forest stand structure, species composition, and carbon sequestration potential. The study aligns with similar research in Nepal's Chitwan-Annapurna Landscape, emphasizing the importance of understanding species-specific carbon sequestration capacities to address climate change effectively (Subedi et al., 2016).
Table 2: Species-wise biomass (Mg/ha) accumulation and carbon (Mg C/ha) sequestration potential
|
Above ground
|
Below ground
|
Dead Organic Matter
|
Total
|
Species
|
Biomass
(Mg/ha)
|
Carbon
(MgC/ha)
|
Biomass
(Mg/ha)
|
Carbon
(MgC/ha)
|
Biomass
(Mg/ha)
|
Carbon
(MgC/ha)
|
Biomass
(Mg/ha)
|
Carbon
(MgC/ha)
|
Bc
|
0.363
|
0.182
|
0.094
|
0.047
|
0.050
|
0.025
|
0.508
|
0.254
|
Bj
|
0.053
|
0.026
|
0.014
|
0.007
|
0.007
|
0.004
|
0.074
|
0.037
|
Cs
|
0.007
|
0.004
|
0.002
|
0.001
|
0.001
|
0.001
|
0.010
|
0.005
|
Ct
|
1.208
|
0.604
|
0.314
|
0.157
|
0.167
|
0.084
|
1.690
|
0.845
|
Ds
|
0.007
|
0.004
|
0.002
|
0.001
|
0.001
|
0.001
|
0.010
|
0.005
|
Di
|
0.008
|
0.004
|
0.002
|
0.001
|
0.001
|
0.001
|
0.011
|
0.006
|
Ea
|
0.079
|
0.040
|
0.021
|
0.010
|
0.011
|
0.005
|
0.111
|
0.055
|
Ec
|
0.100
|
0.050
|
0.026
|
0.013
|
0.014
|
0.007
|
0.140
|
0.070
|
Ep
|
0.010
|
0.005
|
0.003
|
0.001
|
0.001
|
0.001
|
0.014
|
0.007
|
Mc
|
0.935
|
0.467
|
0.243
|
0.122
|
0.130
|
0.065
|
1.307
|
0.654
|
Pr
|
0.458
|
0.229
|
0.119
|
0.060
|
0.064
|
0.032
|
0.641
|
0.320
|
Pw
|
0.168
|
0.084
|
0.044
|
0.022
|
0.023
|
0.012
|
0.236
|
0.118
|
Pc
|
0.266
|
0.133
|
0.069
|
0.035
|
0.037
|
0.018
|
0.372
|
0.186
|
Qg
|
0.287
|
0.143
|
0.075
|
0.037
|
0.040
|
0.020
|
0.401
|
0.201
|
Qgr
|
0.614
|
0.307
|
0.160
|
0.080
|
0.085
|
0.043
|
0.859
|
0.429
|
Ql
|
0.533
|
0.266
|
0.138
|
0.069
|
0.074
|
0.037
|
0.745
|
0.372
|
Ra
|
0.158
|
0.079
|
0.041
|
0.020
|
0.022
|
0.011
|
0.220
|
0.110
|
Sw
|
0.182
|
0.091
|
0.047
|
0.024
|
0.025
|
0.013
|
0.254
|
0.127
|
Sp
|
0.015
|
0.007
|
0.004
|
0.002
|
0.002
|
0.001
|
0.021
|
0.010
|
Sc
|
0.110
|
0.055
|
0.029
|
0.014
|
0.015
|
0.008
|
0.154
|
0.077
|
Za
|
0.003
|
0.002
|
0.001
|
0.000
|
0.000
|
0.000
|
0.004
|
0.002
|
Zi
|
0.077
|
0.039
|
0.020
|
0.010
|
0.011
|
0.005
|
0.108
|
0.054
|
Mean
|
0.256
|
0.128
|
0.067
|
0.033
|
0.036
|
0.018
|
0.359
|
0.179
|
SD (Standard Deviation)
|
±0.321
|
±0.161
|
±0.084
|
±0.042
|
±0.045
|
±0.022
|
±0.449
|
±0.225
|
3.2.1 Total Biomass (TB) accumulation (Bole Biomass [BB], Above Ground Biomass [AGB], Below Ground Biomass [BGB] and Dead Organic Matter [DOM]) of Gama Luma.
The study area exhibited a total biomass accumulation of 11.438 Mg/ha, with species-specific contributions ranging from 0.782 to 3.548 Mg/ha. Biomass acts as the main organic carbon reservoir in forest ecosystems, influenced by topography, climate, wood density, and volume equations. Ali et al. (2023) further explored the factors affecting biomass accumulation, highlighting plant characteristics such as morphology, genetics, physiology, and environmental factors like air temperature, humidity, light intensity, shading, and soil conditions. The study also underscored the importance of management practices in forestry, silviculture, and ecosystem protection in enhancing biomass production.
3.3 Carbon sequestration potential of Gama Luma study site
The study site in Gama Luma showed an overall carbon sequestration potential of 5.719 Mg C/ha, with individual biomass contributing between 0.391 and 2.821 Mg C/ha (ref. Table 3). Among different species, carbon sequestration varied from 0.003 to 1.225 Mg C/ha. The biomass accumulation and carbon stock quantity is less for the study site since data were collected across 30 sampled plots containing trees with DBH greater than 10 cm. The young age of the forest resulted in a smaller pool for analysis. Despite this limitation, the study provides valuable insights into species with the potential for biomass accumulation and carbon sequestration, aiding in developing effective forest management strategies.
Similarly, in Maleka Parish, Uganda, a research initiative explored the potential for carbon sequestration within smallholder farmlands of 60 farms (including herbs, shrubs, and trees). Results indicated an average of 7.8 Mg C/ha sequestered (Menteri, 2014). This small-scale investigation helped farmers participate in carbon markets, benefiting the environment and their livelihoods.
Table 3: Total biomass (Mg/ha) and carbon (Mg C/ha) sequestration potential
Species
|
BB
|
AGB
|
BGB
|
DOM
|
Total biomass
|
Total carbon
|
Bc
|
0.228
|
0.363
|
0.094
|
0.050
|
0.736
|
0.368
|
Bj
|
0.033
|
0.053
|
0.014
|
0.007
|
0.107
|
0.053
|
Cs
|
0.005
|
0.007
|
0.002
|
0.001
|
0.015
|
0.007
|
Ct
|
0.760
|
1.208
|
0.314
|
0.167
|
2.450
|
1.225
|
Ds
|
0.005
|
0.007
|
0.002
|
0.001
|
0.015
|
0.008
|
Di
|
0.005
|
0.008
|
0.002
|
0.001
|
0.016
|
0.008
|
Ea
|
0.050
|
0.079
|
0.021
|
0.011
|
0.161
|
0.080
|
Ec
|
0.063
|
0.100
|
0.026
|
0.014
|
0.204
|
0.102
|
Ep
|
0.006
|
0.010
|
0.003
|
0.001
|
0.020
|
0.010
|
Mc
|
0.588
|
0.935
|
0.243
|
0.130
|
1.895
|
0.948
|
Pr
|
0.288
|
0.458
|
0.119
|
0.064
|
0.929
|
0.464
|
Pw
|
0.106
|
0.168
|
0.044
|
0.023
|
0.342
|
0.171
|
Pc
|
0.167
|
0.266
|
0.069
|
0.037
|
0.539
|
0.269
|
Qg
|
0.180
|
0.287
|
0.075
|
0.040
|
0.581
|
0.291
|
Qgr
|
0.386
|
0.614
|
0.160
|
0.085
|
1.245
|
0.623
|
Ql
|
0.335
|
0.533
|
0.138
|
0.074
|
1.080
|
0.540
|
Ra
|
0.099
|
0.158
|
0.041
|
0.022
|
0.319
|
0.160
|
Sw
|
0.114
|
0.182
|
0.047
|
0.025
|
0.368
|
0.184
|
Sp
|
0.009
|
0.015
|
0.004
|
0.002
|
0.030
|
0.015
|
Sc
|
0.069
|
0.110
|
0.029
|
0.015
|
0.224
|
0.112
|
Za
|
0.002
|
0.003
|
0.001
|
0.000
|
0.006
|
0.003
|
Zi
|
0.049
|
0.077
|
0.020
|
0.011
|
0.157
|
0.078
|
Total biomass
|
3.548
|
5.641
|
1.467
|
0.782
|
11.438
|
-
|
Total carbon
|
1.774
|
2.821
|
0.733
|
0.391
|
5.719
|
-
|
Abbreviations: BB- Bole Biomass, AGB- Above Ground Biomass, BGB- Below Ground Biomass, DOM- Dead Organic Matter
3.4 Number of trees distributed in DBH class
The study conducted in Gama Luma, Bhutan, examined the distribution of tree diameters at breast height (DBH), revealing a diverse range from 10 to 116.3 cm. Notably, the majority of trees fell within the 10-20 cm DBH class, totaling 168 trees, followed by 72 trees in the 21-30 cm DBH class. In contrast, very few trees were found in the larger DBH classes of 101-110 cm and 111-120 cm, each with only one tree, indicating a forest stand skewed towards smaller diameters typical of a young forest (Figure 4).
3.5 Diameter class (DBH) distribution and biomass accumulation
The study conducted in Gama Luma, Bhutan, analyzed the relationship between diameter at breast height (DBH) classes and biomass accumulation, revealing significant variations across different tree size categories. The DBH class ranging from 10 to 20 cm emerged as dominant in Above Ground Biomass (AGB), recording 1.326 Mg/ha, followed by the 41-50 cm class with 0.994 Mg/ha. Accordingly, the 10-20 cm DBH class also exhibited the highest accumulations in Bole Biomass (BB), Below Ground Biomass (BGB), and Dead Organic Matter (DOM), highlighting its importance in overall biomass storage within the forest ecosystem (ref. Figure 5). In contrast, the largest DBH class (111-120 cm) showed significantly lower biomass accumulations across all categories, indicating the scarcity of older and larger trees in the study area, which predominantly consists of young forest stands.
These findings underscore the impact of forest age structure on biomass accumulation and carbon storage potential. The prevalence of smaller DBH classes with higher biomass accumulations reflects the young nature of the forest in Gama Luma. This analysis directly addresses the study’s objective of quantifying terrestrial biomass accumulation and carbon stock in the ecotone region, offering insights into how different DBH classes influence carbon dynamics and emphasizing the importance of forest management strategies that promote diverse age structures for enhancing carbon sequestration efforts.
Table 4: Biomass (mg/ha) and carbon (mg C/ha) in DBH class
DBH class
(cm)
|
BB
|
AGB
|
BGB
|
DOM
|
Total biomass
(Mg/ha)
|
Total carbon
Mg C/ha)
|
10- 20
|
0.834
|
1.326
|
0.345
|
0.184
|
1.855
|
0.927
|
21-30
|
0.431
|
0.685
|
0.178
|
0.095
|
0.958
|
0.479
|
31-40
|
0.526
|
0.837
|
0.218
|
0.116
|
1.170
|
0.585
|
41-50
|
0.625
|
0.994
|
0.258
|
0.138
|
1.390
|
0.695
|
51-60
|
0.586
|
0.932
|
0.242
|
0.129
|
1.304
|
0.652
|
61-70
|
0.127
|
0.202
|
0.053
|
0.028
|
0.283
|
0.141
|
71-80
|
0.119
|
0.190
|
0.049
|
0.026
|
0.265
|
0.133
|
81-90
|
0.036
|
0.058
|
0.015
|
0.008
|
0.081
|
0.040
|
91-100
|
0.251
|
0.400
|
0.104
|
0.055
|
0.559
|
0.279
|
101-110
|
0.008
|
0.012
|
0.003
|
0.002
|
0.017
|
0.008
|
111-120
|
0.004
|
0.006
|
0.001
|
0.001
|
0.008
|
0.004
|
Total
|
0.295
|
0.469
|
0.122
|
0.065
|
0.657
|
0.328
|
3.6 Diameter class and carbon sequestration
The study in Gama Luma, Bhutan, investigated the carbon sequestration potential across various diameters at breast height (DBH) classes, highlighting that smaller to medium-sized trees, particularly those in the 10-20 cm and 41-50 cm DBH classes, exhibited the highest capability for carbon storage. Specifically, the 10-20 cm DBH class showed the highest carbon sequestration potential at 0.927 Mg C/ha, followed closely by the 41-50 cm class at 0.695 Mg C/ha. Larger trees in the DBH classes exceeding 71 cm up to 111-120 cm demonstrated lower carbon stocks due to fewer individual trees in these size categories. This pattern underscores the importance of tree size in determining carbon storage capacity within the forest ecosystem of Gama Luma.
Comparative studies from Himachal Pradesh and Myanmar provide additional context on how DBH size influences carbon sequestration potential in forest ecosystems. The research from Himachal Pradesh indicated that the 21-30 cm DBH class exhibited the greatest capability for carbon storage across diverse forest locations, emphasizing the role of mature forest stands in storing larger amounts of carbon compared to younger stands. In contrast, findings from Myanmar's mangrove plantations suggested that trees in the 11-20 cm DBH range showed higher carbon storage potential than those in other DBH size classes, highlighting the variability in carbon sequestration potential influenced by both species’ composition and tree size. These insights contribute to a broader understanding of the relationship between forest structure, species characteristics, and carbon dynamics, which are essential for effective forest management and climate change mitigation strategies.
3.7 Relationship analysis between DBH and Carbon stock (Mg C/ha)
Spearman correlation test generated a statistically significant relationship between the DBH distribution and carbon (C) sequestration potential with r = 0.774** at p < 0.05 (2-tailed). It suggests that the tendency for carbon sequestration increases as the diameter at breast height of trees increases.
Understanding the correlation between diameter at breast height (DBH) distribution and carbon storage is crucial for implementing successful forest management techniques and strategies to combat climate change (Dorji et al., 2021; Ahmed et al., 2023). Different DBH classes signify different phases of tree development and biomass accumulation, influencing forests' overall capacity to sequester carbon.
Examining the relationship between diameter class and carbon sequestration potential directly addresses the research question of how diameter at breast height (DBH) class influences biomass accumulation and carbon sequestration potential. The statistically significant correlation between DBH distribution and carbon sequestration underscores the importance of considering tree size in forest management strategies to enhance carbon storage.