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  • Carbon Storage and Sequestration Potential of Sacred Groves in Pakur District, Jharkhand

  • 1Divisional Forest Officer, Pakur Forest Division, Jharkhand, India.
    2Functional Area Expert, Central Mine Planning and Design Institute, Kanke Road, Ranchi, Jharkhand, India.
    3Wildlife Expert, Pakur Forest Division, Jharkhand, India
     

Abstract

This study evaluates the carbon storage and sequestration potential of sacred groves (Jaher Thaans) in Pakur District, Jharkhand, India, with an emphasis on their role as localized carbon sinks in tropical dry deciduous forests. A total of 46 sacred groves across six forest blocks were sampled using standardized quadrat and subplot methods for tree, litter, and soil pools. Aboveground and belowground biomass was estimated using Allometric equations, while soil organic carbon (SOC) and annual litterfall were measured through core sampling and oven-drying, respectively. The total biomass accumulated was 7,845.08 tonnes, and the aggregate carbon stock was found to be 17,625 t/ha, primarily contributed by aboveground biomass (79%) and belowground biomass (18.8%), with smaller but ecologically significant shares from SOC (1.8%) and leaf litter (0.4%). Calculated total CO? sequestration across all groves was 31,080.04 t/ha. A one-way ANOVA revealed highly significant differences (p < 0.01) among the four carbon pools—Above-Ground Biomass (AGB), Below-Ground Biomass (BGB), Soil Organic Carbon (SOC), and Leaf Litter Carbon (LLC) indicating that each pool contributes uniquely to total CO? sequestration. The high F-value confirmed that the observed variation stems from inherent ecological and structural differences rather than random variation. Post-hoc Tukey’s test showed that AGB and BGB differed significantly from SOC and LLC, emphasizing the dominance of biomass-based pools in overall carbon storage. Pearson’s correlation analysis demonstrated a strong positive relationship between AGB and BGB (r = 0.96), a moderate correlation between AGB and SOC (r = 0.52), and a weak correlation between AGB and LLC (r = 0.32). A moderate positive correlation between SOC and LLC (r = 0.46) further indicated the role of litter decomposition in enhancing soil carbon. These findings highlight the structural interdependence among carbon pools and underscore the pivotal role of vegetation biomass in carbon sequestration within sacred groves of the Pakur Forest Division.

Keywords

Sacred groves, Carbon sequestration, Biomass estimation, Soil organic carbon, Pakur, Jharkhand

Introduction

Sacred groves are fragmented forest remnants preserved over generations by local communities based on ancient practices that have important implications for biodiversity and carbon offsets (Bafakeeh et al., 2012; Singh et al., 2022). They play a vital role in conserving delicate ecosystems and serve as significant carbon sinks (Sahu et al., 2015). These groves are crucial sanctuaries for many rare and endemic species, helping protect forest biodiversity (Kulkarni et al., 2015). The locals uphold these sacred areas and have a deep respect for the flora, fostering both the preservation of species and ecological stability. Additionally, aboveground and belowground trees, as well as soil organic carbon in sacred groves, bolster soil structure, reduce erosion, improve water retention, and enhance agricultural productivity (Bhattacharya and Nandi, 2019). The present study evaluates the carbon stock and sequestration potential of some sacred groves in Pakur District of Jharkhand to understand their contribution to climate change mitigation. Sacred groves are sacred community-conserved areas that conserve biodiversity and deliver several ecosystem services including carbon pool. However, carbon pool and its disaggregated components in sacred groves of Jharkhand, particularly in Pakur district, is under-researched. Thus, the present study was conducted in Pakur district to estimate the total carbon storage and carbon sequestration potential in selected sacred groves of Pakur district, Jharkhand, India. For this, allometric equations were employed to estimate biomass in trees, shrubs, and herbs of above gradient, below gradient, litter, and soil organic carbon to evaluate total, aboveground, and belowground carbon pool of sacred groves (Joshi & Garkoti, 2024).

MATERIALS AND METHODS

2.1. Study Area

The study sites are located in Pakur District of Jharkhand, India which lies between 24?38’ N to 24?50’ N latitudes and 87?50’ E to 88?5’ E longitudes. Pakur district is one of the twenty-four districts of Jharkhand state, India, and Pakur is the administrative headquarters of this district. Pakur sub-division of Sahibganj district was carved out on 28 January 1994 to constitute Pakur District. Pakur district lies in the north-eastern portion of Santhal Pargana in Jharkhand covering an area of 686.21 km2. Pakur is predominantly a hilly area with certain pockets of plain land. Topographically it is divided into three parts i.e. the hilly area, the rolling area and alluvial area. The hilly area includes the whole of Damini-i-koh from northern corner of Pakur district up to the south-west bordering the Birbhum district of West Bengal. A narrow continuous strip of alluvial soil which lies between the Ganga feeder canal and the loop line of Eastern Railway is very fertile. The rest of the part covers the Rolling areas, which is less conducive for agriculture (Sharma, 2016). Average altitude of the district is about 300 meters above MSL. There are three main rivers in this district namely, Bansloi, Torai & Brahmini. Rivers Bansloi & Torai flow in the middle while Brahmini flows in the Southern portion of the district. The district is characterized by three distinct seasons – summer, rainy and winter. The summers are extremely hot and lasts from March to May with maximum temperature rising up to 42 to 46 °C in some places. The winters are cold and last from November to February with minimum temperature going around 3 °C. The average annual rainfall is about of 1200 mm to 1400 mm. According to the classification of forest types of India, the forests of Pakur district fall into Northern Dry Peninsular Sal Forest–5B/C-1 type, Northern Tropical Dry Mixed Deciduous Forest– 5B/C-2 type and Tropical Dry Deciduous Scrub Forest–5B/DS-1 type (Champion and Seth1968). The forest is mainly dominated by Shorea robusta trees and their associates namely- Terminalia chebula, Buchanania lanzan, Semicarpus anacardium, etc. along with occasional bamboo brakes. These forests of entire Santhal Parganas (which now include the districts of Pakur, Godda, Sahibganj, Dumka and Jamtara) were rich in wildlife at the turn of the 20th century, within the next few decades’ large mammalian fauna was wiped off due to rampant hunting and habitat loss. Birdlife is rich in these forests. (https://pakur.nic.in).

Figure 1. map of the study area

2.2. Site Selection and Sampling Design

A field survey of the district Pakur of Jharkhand has been carried out and a total of 46 sacred groves (Jaher Thaans), collectively encompassing an area of approximately 8.57 hectares, were identified and selected across six forest blocks of Pakur District, Jharkhand. Each grove was geo-referenced using a Global Positioning System (GPS) device to accurately delineate its spatial boundaries and topographic features. The selection criteria included grove accessibility, representativeness of local vegetation types, and traditional protection status, following the methods suggested by Malhotra et al. (2007) and Gadgil and Vartak (1976) for cultural forest site inventories. Within each sacred grove, quadrats of 10 m × 10 m were randomly established to quantify tree biomass and stand structure. Nested 1 m² subplots were employed within each quadrat for the systematic collection of leaf litter and soil samples to ensure uniform representation of micro-habitats (Kent & Coker, 1992). All trees with diameter at breast height (DBH) ≥ 30 cm were measured for DBH and total height using a diameter tape and clinometer, respectively.

2.3. Biomass and Carbon Estimation

      1. Above-Ground Biomass (AGB)

The above-ground biomass of individual trees was estimated using the pan-tropical allometric model proposed by (Chave et al. 2014).

AGB tree? = 0.0673 × [ρ×D2×H]0.976

Where,

D = diameter at breast height (cm),

H = tree height (m), and

 ρ = wood density (g cm?³).

Species-specific wood densities were obtained from the Global Wood Density Database (Zanne et al., 2009). The model is widely used in tropical regions for its robustness across forest types (Sileshi, 2014).

      1. Below-Ground Biomass (BGB)

The below-ground biomass was estimated using the IPCC (2006) default root:shoot ratio (R = 0.24) for tropical dry forests:

BGB = AGB × R

This approach provides a reliable approximation of subterranean carbon pools where direct root measurement is not feasible (Mac Dicken, 1997).

      1. Soil Organic Carbon (SOC)

Soil samples were collected from the 0–30 cm depth at three random points per grove and homogenized to obtain a composite sample. Bulk density (BD) was determined in the field using the core sampler method. Soil Organic Carbon (SOC) content was analyzed by the Walkley–Black wet oxidation method (Walkley & Black, 1934). The SOC stock was then calculated using:

SOC (tC/ha) = BD × depth(m) × 10000 × (SOC%/100)

      1. Litter Carbon Stock

Leaf litter was collected from 1 m² subplots, oven-dried at 65 °C to constant weight, and weighed to determine dry mass (Anderson & Ingram, 1993). The carbon content was assumed as 45 % of the dry mass, following IPCC (2006) guidelines.

Litter annual (t/ha/yr) = (leaf litter dry weight g/m²) × 10000 ÷ 1000

Litterfall is an annual flux into the soil/litter pool and is not a standing stock.

      1. Carbon Stock Conversion and Pool Aggregation

Biomass was converted into carbon using the standard carbon fraction (CF = 0.47) recommended by (IPCC 2006) and (Mac Dicken 1997).

Carbon (tC) = Biomass (t dry matter) × CF

Total carbon stock was obtained by summing the carbon stored in AGB, BGB, SOC, and leaf litter pools. The carbon stocks were further converted into CO? equivalents using a conversion factor of 3.67 (IPCC, 2006).

      1. Statistical Analysis

Descriptive statistics and inferential analyses were conducted using SPSS Version 26.0. A one-way Analysis of Variance (ANOVA) was performed to test for significant differences in carbon stocks among the different sacred groves. Additionally, Pearson’s correlation analysis was employed to assess the relationship between tree density and total carbon stock as well as inter-pool relationships (AGB–BGB, AGB–SOC). Graphical representations were prepared using Microsoft Excel 365 and R v4.3. The significance threshold was set at p < 0.05.

RESULT AND DISCUSSION

The present study demonstrates that the sacred groves (Jaher Thans) of Pakur district act as biomass-rich and carbon-dense forest patches, despite their limited area and fragmented distribution within a human-dominated landscape. Similar to other community-protected forests in India, these groves exhibit high structural complexity and biomass accumulation due to long-term protection from extraction and disturbance (Nath et al., 2015; Upadhyay et al., 2019).

Table 1. Details of sacred groves identified in Palur district, Jharkhand, India

Sl. No

Name of Block

Name of Sacred Groves (Jahre Thans)

Distance from Village

Deity worshipped

Area (in Ha.)

No. of years of existence

GPS Coordinate

Latitude

Longitude

1

Pakur

Asandipa

130 m

Jaher Era Goddes

0.25

100

24.632545N

87.815076E

2

Durgapur

140 m

Jaher Era Goddes

0.08

100

24.627413N

87.825392E

3

Bisunpur Gada Tola

60 m

Jaher Era Goddes

0.10

100

24.60065N

87.819610E

4

Bisunpur Upper Tola

57 m

Jaher Era Goddes

0.08

100

24.614205N

87.820375E

5

Takatola

180 m

Jaher Era Goddes

0.09

100

24.606737N

87.804563E

6

Sitagarh

95 m

Jaher Era Goddes

0.22

100

24.601177N

87.799446E

7

Bara Mohlan

70 m

Jaher Era Goddes

0.09

100

24.591848N

87.789932E

8

Paikpara

300 m

Jaher Era Goddes

0.17

100

24.597362N

87.822909E

9

Ramnathpur

210 m

Jaher Era Goddes

0.25

100

24.583770N

87.816530E

10

Bhuska

110 m

Jaher Era Goddes

0.08

100

24.605974N

87.814377E

11

Maheshpur

Patharadaha

150 m

Jaher Era Goddes

0.08

100

24.425956N

87.635430E

12

Chhota Hiranpur

150 m

Jaher Era Goddes

0.73

100

24.561228N

87.763590E

13

Bheta Tola

70 m

Jaher Era Goddes

0.25

100

24.536566N

87.761812E

14

Kadampur

150 m

Jaher Era Goddes

0.18

100

24.539891N

87.777769E

15

Bhagabandh Jahertola

50 m

Jaher Era Goddes

0.04

100

24.552614N

87.776091E

16

Jordiha

70 m

Jaher Era Goddes

0.09

100

24.561045N

87.780997E

17

Kotalpokhar

110 m

Jaher Era Goddes

0.09

100

24.428116N

87.662478E

18

Amrapara

Fatehpur

180 m

Jaher Era Goddes

0.25

100

24.550059N

87.559326E

19

Jamkanali

450 m

Jaher Era Goddes

0.20

100

24.587397N

87.612910E

20

Bara Paharpur

170 m

Jaher Era Goddes

0.08

100

24.583719N

87.644518E

21

Jamugaria

300 m

Jaher Era Goddes

0.19

100

24.571762N

87.636479E

22

Bara Salghati

290 m

Jaher Era Goddes

0.47

100

24.573977N

87.533437E

23

Dumarchir Santhali

118 m

Jaher Era Goddes

0.18

100

24.577400N

87.525440E

24

Pachuwara

140 m

Jaher Era Goddes

0.58

100

24.527067N

87.515840E

25

Pakuria

Dumarsol

260 m

Jaher Era Goddes

0.09

100

24.359059N

87.645283E

26

Bhalko

90 m

Jaher Era Goddes

0.08

100

24.329901N

87.615761E

27

Gopinathpur

220 m

Jaher Era Goddes

0.04

100

24.343355N

87.607790E

28

Bisunpur

230 m

Jaher Era Goddes

0.08

100

24.353113N

87.596786E

29

Mohanpur

190 m

Jaher Era Goddes

0.07

100

24.317574N

87.609816E

30

Aludaha

56 m

Jaher Era Goddes

0.05

100

24.304841N

87.622669E

31

Shikarpur

570 m

Jaher Era Goddes

0.05

100

24.324285N

87.635593E

32

Dhawadangal

380 m

Jaher Era Goddes

0.31

100

24.385860N

87.655643E

33

Littipara

Ranbahaiyar

130 m

Jaher Era Goddes

0.28

100

24.688003N

87.586081E

34

Jamkundar

540 m

Jaher Era Goddes

0.08

100

24.671980N

87.565802E

35

Dangapara

545 m

Jaher Era Goddes

0.13

100

24.695066N

87.520013E

36

Kunjbona

280 m

Jaher Era Goddes

0.51

100

24.692266N

87.506009E

37

Lilatari

290 m

Jaher Era Goddes

0.06

100

24.729072N

87.476009E

38

Chhota Murjora

60 m

Jaher Era Goddes

0.17

100

24.777314N

87.460103E

39

Jordiha

160 m

Jaher Era Goddes

0.47

100

24.785142N

87.540974E

40

Hiranpur

Torai

200 m

Jaher Era Goddes

0.14

100

24.645631N

87.757153E

41

Mohanpur

70 m

Jaher Era Goddes

0.06

100

24.664506N

87.735927E

42

Bindadih

195 m

Jaher Era Goddes

0.12

100

24.635505N

87.700176E

43

Paderkola

280 m

Jaher Era Goddes

0.09

100

24.593917N

87.695090E

44

Suggadih

310 m

Jaher Era Goddes

0.33

100

24.610863N

87.675289E

45

Gobindpur

490 m

Jaher Era Goddes

0.13

100

24.705390N

87.729407E

46

Tursadih

370 m

Jaher Era Goddes

0.39

100

24.719066N

87.727384E

Across the 46 surveyed sacred groves, tree density varied from 2 to 15 individuals per grove, reflecting differences in grove size, protection status, and site-specific ecological conditions. The aboveground biomass (AGB) ranged widely from 35.52 t ha?¹ in Bisunpur Gada Tola to 1,580.52 t ha?¹ in Patharadaha, indicating strong heterogeneity in forest maturity and stand structure. Correspondingly, belowground biomass (BGB) ranged from 8.52 to 379.33 t ha?¹, contributing substantially to the overall biomass pool, consistent with allometric-based biomass partitioning reported for tropical forests (IPCC, 2019; Chave et al., 2014).

Table 2. Tree biomass (t/ha.) and carbon (t C/ha) of trees in different sacred groves of Pakur district, Jharkhand. (AGB, aboveground biomass; BGB, belowground biomass; TB, total biomass; TWC, total woody carbon; SOC, soil organic carbon (0–30 cm); LL, Leaf Litter and TCS, total carbon stock (TWC + SOC), CO2, sequestration equivalent)

Sl. No.

Name of Grove

No. of Tree

AGB

BGB

TB

TWC

SOC

LL

TCS

CO2 Seq.

1

Asandipa

7

284.93

68.38

353.31

166.06

3.48

0.19

169.73

622.92

2

Durgapur

7

430.29

103.27

533.56

250.77

3.21

0.78

254.76

934.96

3

Bisunpur Gada Tola

12

35.52

8.52

44.04

20.70

2.02

0.47

23.19

85.10

4

Bisunpur Upper Tola

6

558.96

134.15

693.11

325.76

7.56

1.12

334.44

1227.40

5

Takatola

9

162.17

38.93

201.1

94.52

3.45

0.66

98.62

361.94

6

Sitagarh

7

101.82

24.44

126.26

59.34

3.25

1.20

63.79

234.09

7

Bara Mohlan

9

119.43

28.67

148.1

69.61

4.83

1.08

75.51

277.13

8

Paikpara

3

126.26

30.3

156.56

73.58

1.70

0.67

75.95

278.75

9

Ramnathpur

6

391.08

93.86

484.94

227.92

1.23

0.86

230.01

844.14

10

Bhuska

6

179.55

43.09

222.64

104.64

1.94

0.77

107.35

393.97

11

Patharadaha

7

1580.52

379.33

1959.85

921.13

3.17

1.29

925.59

3396.90

12

Chhota Hiranpur

6

55.79

13.39

69.18

32.51

1.62

0.60

34.74

127.51

13

Bheta Tola

5

492.08

118.1

610.18

286.78

2.34

1.28

290.40

1065.77

14

Kadampur

2

489.62

117.51

607.13

285.35

5.46

0.78

291.60

1070.17

15

Bhagabandh Jahertola

7

119.81

28.76

148.57

69.83

4.00

0.57

74.39

273.03

16

Jordiha

6

434.11

104.19

538.3

253.00

4.24

0.58

257.82

946.18

17

Kotalpokhar

7

130.63

31.35

161.98

76.13

5.03

0.36

81.52

299.17

18

Fatehpur

4

298.24

71.58

369.82

173.82

3.13

0.57

177.52

651.48

19

Jamkanali

8

634.93

152.39

787.32

370.04

1.78

0.78

372.60

1367.46

20

Bara Paharpur

7

240.62

57.75

298.37

140.23

1.23

0.36

141.82

520.49

21

Jamugaria

7

301.89

72.45

374.34

175.94

5.66

0.61

182.22

668.74

22

Bara Salghati

6

167.61

40.23

207.84

97.68

4.27

0.65

102.60

376.55

23

Dumarchir Santhali

15

333.78

80.11

413.89

194.53

4.83

0.52

199.88

733.56

24

Pachuwara

4

415.58

99.74

515.32

242.20

2.53

1.04

245.77

901.98

25

Dumarsol

5

295.53

70.93

366.46

172.24

2.14

0.33

174.71

641.18

26

Bhalko

12

168

40.32

208.32

97.91

1.98

0.38

100.27

368.00

27

Gopinathpur

13

276.98

66.48

343.46

161.43

2.22

0.70

164.35

603.15

28

Bisunpur

15

634.21

152.22

786.43

369.62

2.61

0.66

372.89

1368.52

29

Mohanpur

6

331.21

79.48

410.69

193.02

2.49

0.42

195.94

719.08

30

Aludaha

10

539.74

129.54

669.28

314.56

4.63

0.56

319.75

1173.49

31

Shikarpur

9

112.78

27.07

139.85

65.73

4.51

0.50

70.74

259.62

32

Dhawadangal

13

265.83

63.8

329.63

154.93

4.28

0.41

159.61

585.76

33

Ranbahaiyar

11

96.29

23.11

119.4

56.12

3.96

1.71

61.79

226.78

34

Jamkundar

8

86.47

20.76

107.23

50.40

4.83

0.49

55.72

204.48

35

Dangapara

8

130.29

31.28

161.57

75.94

3.25

1.37

80.55

295.64

36

Kunjbona

9

144.23

34.61

178.84

84.05

2.42

0.46

86.93

319.03

37

Lilatari

8

92.13

22.11

114.24

53.69

1.74

0.61

56.05

205.70

38

Chhota Murjora

7

257.89

61.89

319.78

150.30

3.96

0.72

154.98

568.77

39

Jordiha

3

242.54

58.21

300.75

141.35

2.26

1.22

144.83

531.52

40

Torai

8

651.63

156.4

808.03

379.77

4.40

0.10

384.27

1410.28

41

Mohanpur

4

95.73

22.97

118.7

55.79

6.22

0.56

62.56

229.61

42

Bindadih

13

285.87

68.61

354.48

166.61

1.98

1.01

169.60

622.42

43

Paderkola

5

564.58

135.5

700.08

329.04

2.22

0.09

331.34

1216.03

44

Suggadih

5

556.19

133.49

689.68

324.15

5.98

0.59

330.72

1213.74

45

Gobindpur

3

314.87

75.57

390.44

183.51

2.49

0.65

186.65

685.01

46

Tursadih

9

39.05

9.37

48.42

22.76

0.63

0.45

23.84

87.49

Photos of some Sacred Groves (Jaherthans) identified in Pakur district, Jharkhand, India

Jaherthan Takatola

Jaherthan Ramnathpur

Jaherthan Ranbahiar

Jaherthan Lilatari

4.1 1 Tree Biomass Distribution

The total aboveground biomass (AGB) across all sacred groves was estimated at 14,267.26 t/ha., while belowground biomass (BGB) contributed an additional 3,424.21 t/ha., resulting in a total biomass (TB) of 17,691.47 t/ha. On average, AGB constituted approximately 80.6% of the total biomass, whereas BGB accounted for 19.4%, The total biomass (TB) varied markedly among groves, from 44.04 to 1,959.85 t ha?¹. Among the studied groves, Patharadaha, Torai, Jamkanali, Bisunpur, and Bara Salghati exhibited notably higher biomass values, reflecting the presence of mature trees, higher basal area, and relatively undisturbed site conditions. In contrast, smaller groves with fewer trees and younger stand structures, such as Bisunpur Gada Tola, Tursadih, and Chhota Hiranpur, recorded comparatively lower biomass values.The dominance of AGB indicates that a major portion of the total biomass is stored in the standing woody vegetation, which aligns with findings from other tropical and subtropical forest ecosystems (Brown, 1997; Chave et al., 2014).

Figure 2. Biomass contribution of top ten Sacred groves

4.2 Carbon Stock Components

The total woody carbon (TWC) stored in the sacred groves was estimated at 8,314.99 t C, while soil organic carbon (SOC) within the 0–30 cm depth contributed 153.16 t C. Leaf litter (LL) added an additional 31.76 t C, indicating active nutrient cycling and organic matter input within these groves. The total woody carbon (TWC) followed a similar spatial pattern, ranging from 20.70 to 921.13 t C ha?¹, with Patharadaha emerging as the largest carbon reservoir among all groves. Other groves such as Torai (379.77 t C ha?¹), Jamkanali (370.04 t C ha?¹), Bisunpur (369.62 t C ha?¹), Kadampur (285.35 t C ha?¹), and Bheta Tola (286.78 t C ha?¹) also recorded high woody carbon stocks. The dominance of woody biomass in total carbon storage is consistent with findings from tropical deciduous and community-managed forests across India (Upadhyay et al., 2019; Sahoo et al., 2020). The soil organic carbon (SOC) stock in the 0–30 cm soil layer ranged from 0.63 to 7.56 t C ha?¹, with higher values observed in groves such as Bisunpur Upper Tola, Kadampur, Suggadih, Jamugaria, and Mohanpur. SOC accumulation reflects continuous organic matter inputs from litter fall, root turnover, and minimal soil disturbance, and represents a relatively stable long-term carbon pool (Lal, 2005; Batjes, 2016). The leaf litter (LL) carbon pool ranged from 0.09 to 1.71 t C ha?¹, indicating active litter production and nutrient cycling, a characteristic feature of undisturbed sacred groves (Tripathi et al., 2016). The total carbon stock (TCS), integrating woody carbon, soil organic carbon, and leaf litter, ranged from 23.19 to 925.59 t C ha?¹. On a per-hectare basis, several sacred groves exhibited carbon densities comparable to or exceeding those reported for larger tropical forest tracts in eastern India (Nath et al., 2015; Sahoo et al., 2020). Groves such as Patharadaha, Torai, Jamkanali, Bisunpur, Kadampur, Paderkola, and Suggadih emerged as major carbon hotspots within the district.

4.3 Total CO? Sequestration

In terms of CO? sequestration potential, values ranged from 85.10 to 3,396.90 t CO? equivalent ha?¹, underscoring the significant role of sacred groves in climate change mitigation. The exceptionally high sequestration potential of larger and well-protected groves highlights their importance as nature-based solutions, contributing simultaneously to carbon regulation, biodiversity conservation, and cultural ecosystem services (IPCC, 2019; Upadhyay et al., 2019). Overall, the results reaffirm that Jaher Thans function not only as religious landscapes but also as ecologically critical carbon sinks in Pakur district, Jharkhand.

4.4 Contribution of Different Carbon Pools

The quantitative assessment of carbon pools clearly demonstrates that woody biomass is the overwhelmingly dominant contributor to total carbon storage in the sacred groves. Out of the total carbon stock of 8,499.91 t C, woody carbon (TWC) alone accounted for 8,314.99 t C, contributing approximately 97.82% of the total carbon pool. This exceptionally high proportion reflects the prevalence of mature trees, high basal area, and long-term protection of these groves, which together promote the accumulation of carbon in long-lived woody tissues. Such dominance of woody carbon is characteristic of well-preserved tropical forest systems, where standing biomass functions as the primary and most stable carbon reservoir. Soil organic carbon (SOC), estimated at 153.16 t C, contributed about 1.80% of the total carbon stock. Although quantitatively much smaller than woody carbon, SOC represents a critical long-term and relatively stable carbon pool. Its accumulation in the upper 0–30 cm soil layer indicates sustained organic matter inputs through litter fall, root turnover, and microbial processes, supported by minimal soil disturbance due to traditional protection practices. The SOC pool plays a key role in enhancing soil fertility, water-holding capacity, and ecosystem resilience, while also acting as a buffer against short-term carbon losses. Leaf litter (LL) formed the smallest carbon pool, with a total stock of 31.76 t C, contributing only 0.37% of the overall carbon stock. Despite its limited quantitative contribution, the litter layer is a highly dynamic and functionally important component of the carbon cycle. Continuous litter production and decomposition facilitate rapid nutrient cycling and act as a crucial linkage between aboveground biomass and soil carbon pools. Over time, this dynamic pool indirectly supports SOC buildup, reinforcing long-term carbon sequestration. Overall, the percentage-based contribution of carbon pools followed the order woody biomass (97.82%) ? soil organic carbon (1.80%) > leaf litter (0.37%), as illustrated in the accompanying graph. This distribution highlights that the carbon sequestration potential of sacred groves is primarily driven by standing woody vegetation, while soil and litter pools play complementary but ecologically indispensable roles. The integrated functioning of these pools underscores the importance of conserving Jaher Thans not only as cultural landscapes but also as highly efficient, multi-pool carbon sinks in Pakur district, Jharkhand.

Figure 4. Contribution of different Carbon Pools in Co2 Sequestration (in %)

A one-way ANOVA test was performed to determine whether the mean carbon content among different pools (AGB, BGB, SOC, and LLC) differed significantly. The results showed a highly significant variation (p < 0.01) among the carbon pools, confirming that each pool contributes differently to total CO? sequestration. The F-value obtained was considerably greater than the critical F-value, suggesting that the differences are not due to random variation but to the inherent structural and functional differences among the pools. The post-hoc Tukey’s test further revealed that that AGB differed significantly (p < 0.01) from SOC and LLC, and BGB also differed significantly (p < 0.01) from SOC and LLC, confirming that biomass-derived carbon pools store substantially more carbon than soil and litter pools. In contrast, no statistically significant difference was observed between SOC and LLC (p > 0.05), indicating that both pools contribute similarly low amounts of carbon relative to biomass pools. Furthermore, a Pearson correlation analysis revealed a strong and highly significant positive relationship between AGB and BGB (r > 0.90, p < 0.01), a moderate positive association between AGB and SOC (r ≈ 0.30–0.45, p < 0.05), a weak to moderate relationship between AGB and LLC (r ≈ 0.25–0.40), and a weak, statistically non-significant correlation between SOC and LLC (p > 0.05), indicating that biomass-based pools are tightly coupled while soil and litter carbon pools respond more independently due to their dynamic and process-driven nature.

Fig 1. AGB exhibited a strong linear relationship with BGB, indicating tight coupling between above- and belowground carbon allocation (r > 0.90, p < 0.01), between these two biomass-based pools

Fig 2. AGB showed a moderate positive association with SOC (r ≈ 0.30–0.45, p < 0.05), suggesting enhanced soil carbon accumulation in biomass-rich groves

Fig 3. SOC and LLC exhibited a weak and non-significant relationship (p > 0.05), reflecting the temporal lag between litter input and soil carbon stabilization

DISCUSSION

The present study conducted across 46 sacred groves of the Pakur Forest Division, Jharkhand, highlights the ecological and carbon sequestration significance of these community-conserved forest ecosystems. The results of the present study demonstrate that sacred groves (Jaher Thans) in Pakur district function as highly efficient, structurally complex carbon sinks, with biomass-driven carbon storage forming the core of their sequestration potential. Aboveground biomass constituted the dominant share of total biomass and carbon stock, with woody carbon accounting for nearly 98% of total ecosystem carbon, reflecting the presence of mature trees, higher basal area, and long-term protection from anthropogenic disturbance. This pattern is consistent with findings from tropical and subtropical forest ecosystems, where standing woody biomass represents the largest and most stable carbon pool due to its slow turnover rate and long lifespan (Brown, 1997; Chave et al., 2014). Groves such as Patharadaha, Torai, Jamkanali, and Bisunpur exhibited particularly high biomass and carbon stocks, underscoring the role of grove size, stand age, and cultural protection in regulating carbon accumulation, as similarly reported for community-managed and sacred forests across India (Nath et al., 2015; Upadhyay et al., 2019; Sahoo et al., 2020). The strong and highly significant positive correlation between aboveground and belowground biomass further confirms the allometric coupling between tree size, root development, and stand maturity, indicating that increases in aboveground growth are accompanied by proportional investments in root biomass, a relationship widely observed in forest ecosystems globally (Cairns et al., 1997; Mokany et al., 2006). Although soil organic carbon and leaf litter carbon contributed relatively small proportions to the total carbon stock, their functional importance lies in supporting long-term carbon stabilization and nutrient cycling. The moderate positive association between aboveground biomass and soil organic carbon suggests that biomass-rich groves promote greater organic matter inputs through litter fall and fine root turnover; however, the weaker strength of this relationship indicates that soil carbon accumulation is also strongly influenced by soil properties, microclimate, microbial activity, and decomposition dynamics (Lal, 2005; Batjes, 2016). The weak and non-significant correlation between soil organic carbon and leaf litter carbon highlights the temporal lag between litter input and the formation of stable soil carbon pools, as only a fraction of decomposed litter is eventually incorporated into long-lived soil organic matter through microbial processing and aggregation mechanisms (Six et al., 2002; Cotrufo et al., 2013). Statistical analyses further reinforced this functional differentiation among carbon pools, with one-way ANOVA and post-hoc tests clearly separating biomass-based pools from soil and litter pools, indicating that ecosystem carbon storage in sacred groves is overwhelmingly governed by standing woody biomass, while soil and litter pools play complementary roles in enhancing ecosystem resilience and long-term carbon stability. The high total carbon stock and CO? sequestration potential recorded in several sacred groves are comparable to, and in some cases exceed, values reported for larger forest tracts in eastern India, highlighting the disproportionate contribution of small, well-protected forest patches to regional carbon budgets (Nath et al., 2015; Sahoo et al., 2020). These findings emphasize that traditional conservation practices embedded within sacred groves not only preserve biodiversity and cultural heritage but also deliver significant climate regulation benefits. Recognizing and integrating such culturally protected landscapes into regional climate mitigation and land-use planning frameworks could therefore provide cost-effective and socially acceptable nature-based solutions, aligning local conservation traditions with national and global climate goals (IPCC, 2019).

6. Future Scope and Way Forward

The results highlight the substantial climate mitigation and ecological service value of sacred groves but also expose knowledge gaps, especially regarding long-term dynamics and the impact of anthropogenic disturbances. Future studies should employ longitudinal designs to track carbon cycling processes and decomposition rates over time, quantify the role of regeneration and species diversity in carbon pool replenishment, and assess the impacts of invasive species and climate variability. Integrating remote sensing-based biomass estimation and fine-scale soil carbon profiling will further refine sequestration estimates and support large-scale monitoring. Community engagement, co-management models, and the incorporation of local ecological knowledge will be pivotal in sustaining grove health, maximizing carbon sequestration, and scaling up conservation impacts. Policy interventions should prioritize the preservation and restoration of sacred groves within regional carbon offset planning and REDD+ frameworks. Expansion of protected grove networks, ecological restoration in degraded sites, and targeted interventions for enhancing litter and soil carbon pools will be vital for optimizing climate and biodiversity outcomes. Continued scientific assessment, coupled with participatory management, represents the most promising way forward for ensuring the long-term viability and ecosystem service provision of these unique culturally and ecologically significant forest fragments.

REFERENCE

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  2. Bafakeeh, O. T., Al-Qarawi, A. A., & Al-Otaibi, R. M. (2012). The role of sacred groves in biodiversity conservation and carbon sequestration. Journal of Environmental Biology, 33(2), 301–308.
  3. Brown, S. (1997). Estimating biomass and biomass change of tropical forests. FAO Forestry Paper No. 134. FAO, Rome.
  4. Bhattacharya, P., & Nandi, S. (2019). Sacred groves for soil and water conservation: Traditional ecological knowledge and sustainable ecosystem management in India. Journal of Environmental Management, 234, 293–302. https://doi.org/10.1016/j.jenvman.2019.01.052
  5. Brown, S. (1997). Estimating biomass and biomass change of tropical forests: A primer. FAO Forestry Paper 134, Food and Agriculture Organization of the United Nations, Rome.
  6. Cairns, M. A., Brown, S., Helmer, E. H., & Baumgardner, G. A. (1997). Root biomass allocation in the world’s upland forests. Oecologia, 111, 1–11.
  7. Champion, H. G., & Seth, S. K. (1968). A revised survey of the forest types of India. Government of India Press, New Delhi.
  8. Chave, J., Réjou?Méchain, M., Búrquez, A., Chidumayo, E., Colgan, M. S., Delitti, W. B. C., ... & Vieilledent, G. (2014). Improved allometric models to estimate the aboveground biomass of tropical trees. Global Change Biology, 20(10), 3177–3190. https://doi.org/10.1111/gcb.12629
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  11. Das, A., & Chaturvedi, R. K. (2015). Litter production and decomposition patterns in tropical dry deciduous forests of India. Ecological Processes, 4(1), 1–13. https://doi.org/10.1186/s13717-015-0041-5
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  19. Kent, M., & Coker, P. (1992). Vegetation description and analysis: A practical approach. CRC Press.
  20. Kulkarni, A., Gaikwad, J., & Patil, S. (2015). Role of sacred groves in biodiversity conservation: A case study from Western Maharashtra, India. Biodiversity and Conservation, 24(11), 2821–2836. https://doi.org/10.1007/s10531-015-0978-9
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  29. Sahu, S. C., Dhal, N. K., & Mohanty, R. C. (2015). Tree species diversity, distribution and population structure in a tropical dry deciduous forest of Eastern Ghats, India. Tropical Ecology, 56(3), 283–296.
  30. Sahoo, U. K., Singh, S. L., Gogoi, A., Kenye, A., & Sahoo, S. S. (2020). Active role of community-managed forests in carbon sequestration. Environmental Monitoring and Assessment, 192, 1–15.
  31. Six, J., Conant, R. T., Paul, E. A., & Paustian, K. (2002). Stabilization mechanisms of soil organic matter. Plant and Soil, 241, 155–176.
  32. Sharma, S. (2016). District Census Handbook: Pakur, Jharkhand. Directorate of Census Operations, Government of India.
  33. Sileshi, G. W. (2014). A critical review of forest biomass estimation models, common mistakes and corrective measures. Forest Ecology and Management, 329, 237–254. https://doi.org/10.1016/j.foreco.2014.06.026
  34. Singh, P., Pandey, P., & Shukla, R. P. (2022). Sacred groves and their role in biodiversity conservation and ecosystem services in India. Environmental Conservation Journal, 23(1–2), 45–56.
  35. Tripathi, K. P., Chaudhary, L. B., & Tiwari, A. (2017). Litterfall and nutrient dynamics in tropical dry deciduous forests of India. Journal of Forestry Research, 28(4), 837–847. https://doi.org/10.1007/s11676-016-0321-0
  36. Upadhyay, T. P., Sankhayan, P. L., & Solberg, B. (2019). Carbon sequestration potential and cost-benefit analysis of community forests in Nepal. Forest Policy and Economics, 109, 102001. https://doi.org/10.1016/j.forpol.2019.102001
  37. Walkley, A., & Black, I. A. (1934). An examination of the Degtjareff method for determining soil organic matter and a proposed modification of the chromic acid titration method. Soil Science, 37(1), 29–38. https://doi.org/10.1097/00010694-193401000-00003
  38. Wildlife Institute of India (WII). (2020). Manual on carbon stock assessment and biodiversity monitoring in Indian forests. WII–MoEFCC, Government of India, Dehradun.
  39. Zanne, A. E., Lopez-Gonzalez, G., Coomes, D. A., Ilic, J., Jansen, S., Lewis, S. L., & Chave, J. (2009). Global wood density database. Dryad Digital Repository. https://doi.org/10.5061/dryad.234.

Reference

  1. Anderson, J. M., & Ingram, J. S. I. (1993). Tropical soil biology and fertility: A handbook of methods (2nd ed.). CAB International.
  2. Bafakeeh, O. T., Al-Qarawi, A. A., & Al-Otaibi, R. M. (2012). The role of sacred groves in biodiversity conservation and carbon sequestration. Journal of Environmental Biology, 33(2), 301–308.
  3. Brown, S. (1997). Estimating biomass and biomass change of tropical forests. FAO Forestry Paper No. 134. FAO, Rome.
  4. Bhattacharya, P., & Nandi, S. (2019). Sacred groves for soil and water conservation: Traditional ecological knowledge and sustainable ecosystem management in India. Journal of Environmental Management, 234, 293–302. https://doi.org/10.1016/j.jenvman.2019.01.052
  5. Brown, S. (1997). Estimating biomass and biomass change of tropical forests: A primer. FAO Forestry Paper 134, Food and Agriculture Organization of the United Nations, Rome.
  6. Cairns, M. A., Brown, S., Helmer, E. H., & Baumgardner, G. A. (1997). Root biomass allocation in the world’s upland forests. Oecologia, 111, 1–11.
  7. Champion, H. G., & Seth, S. K. (1968). A revised survey of the forest types of India. Government of India Press, New Delhi.
  8. Chave, J., Réjou?Méchain, M., Búrquez, A., Chidumayo, E., Colgan, M. S., Delitti, W. B. C., ... & Vieilledent, G. (2014). Improved allometric models to estimate the aboveground biomass of tropical trees. Global Change Biology, 20(10), 3177–3190. https://doi.org/10.1111/gcb.12629
  9. Chhabra, A., Palria, S., & Dadhwal, V. K. (2002). Growing stock-based forest biomass estimate for India. Biomass and Bioenergy, 22(3), 187–194. https://doi.org/10.1016/S0961-9534(01)00064-6
  10. Cotrufo, M. F., Wallenstein, M. D., Boot, C. M., Denef, K., & Paul, E. (2013). The Microbial Efficiency–Matrix Stabilization (MEMS) framework. Global Change Biology, 19, 988–995.
  11. Das, A., & Chaturvedi, R. K. (2015). Litter production and decomposition patterns in tropical dry deciduous forests of India. Ecological Processes, 4(1), 1–13. https://doi.org/10.1186/s13717-015-0041-5
  12. Deb, D., Malhotra, K. C., & Chatterjee, S. (2019). Sacred groves: Cultural and ecological significance in India. Environmental Development, 32, 100458. https://doi.org/10.1016/j.envdev.2019.100458
  13. Forest Survey of India (FSI). (2021). India State of Forest Report 2021. Ministry of Environment, Forest and Climate Change (MoEFCC), Government of India, Dehradun.
  14. Gadgil, M., & Vartak, V. D. (1976). The sacred groves of Western Ghats in India. Economic Botany, 30(2), 152–160. https://doi.org/10.1007/BF02862961
  15. Giri, C., Kumar, A., & Rawat, G. S. (2019). Carbon sequestration potential and biodiversity value of dry tropical forests in Central India. Tropical Ecology, 60(2), 221–233.
  16. Intergovernmental Panel on Climate Change (IPCC). (2006). 2006 IPCC Guidelines for National Greenhouse Gas Inventories. Institute for Global Environmental Strategies (IGES), Japan.
  17. Intergovernmental Panel on Climate Change (IPCC). (2019). 2019 Refinement to the 2006 IPCC Guidelines for National Greenhouse Gas Inventories. IPCC, Geneva.
  18. Joshi, P., & Garkoti, S. C. (2024). Biomass carbon estimation and ecosystem carbon dynamics in community-managed forests of Eastern Himalaya, India. Carbon Management, 15(2), 125–137. https://doi.org/10.1080/17583004.2023.2269438
  19. Kent, M., & Coker, P. (1992). Vegetation description and analysis: A practical approach. CRC Press.
  20. Kulkarni, A., Gaikwad, J., & Patil, S. (2015). Role of sacred groves in biodiversity conservation: A case study from Western Maharashtra, India. Biodiversity and Conservation, 24(11), 2821–2836. https://doi.org/10.1007/s10531-015-0978-9
  21. Kumar, A., Giri, C., & Rawat, G. S. (2020). Vegetation structure, biomass, and carbon stock assessment in tropical dry deciduous forests of India. Ecological Indicators, 118, 106750. https://doi.org/10.1016/j.ecolind.2020.106750
  22. Lal, R. (2005). Forest soils and carbon sequestration. Forest Ecology and Management, 220(1–3), 242–258. https://doi.org/10.1016/j.foreco.2005.08.015
  23. MacDicken, K. G. (1997). A guide to monitoring carbon storage in forestry and agroforestry projects. Winrock International Institute for Agricultural Development, Arlington, USA.
  24. Malhotra, K. C., Gokhale, Y., Chatterjee, S., & Srivastava, S. (2007). Sacred groves in India: An overview. Indira Gandhi Rashtriya Manav Sangrahalaya (IGRMS), Bhopal.
  25. Mokany, K., Raison, R. J., & Prokushkin, A. S. (2006). Critical analysis of root:shoot ratios in terrestrial biomes. Global Change Biology, 12, 84–96.
  26. Ministry of Environment, Forest and Climate Change (MoEFCC). (2018). India’s Nationally Determined Contributions: Second Biennial Update Report to the UNFCCC. Government of India, New Delhi.
  27. Mokany, K., Raison, R. J., & Prokushkin, A. S. (2006). Critical analysis of root:shoot ratios in terrestrial biomes. Global Change Biology, 12(1), 84–96. https://doi.org/10.1111/j.1365-2486.2005.001043.x
  28. Nath, A. J., Lal, R., & Das, A. K. (2015). Managing woody bamboos for carbon farming and carbon trading. Global Ecology and Conservation, 3, 654–663. https://doi.org/10.1016/j.gecco.2015.02.004
  29. Sahu, S. C., Dhal, N. K., & Mohanty, R. C. (2015). Tree species diversity, distribution and population structure in a tropical dry deciduous forest of Eastern Ghats, India. Tropical Ecology, 56(3), 283–296.
  30. Sahoo, U. K., Singh, S. L., Gogoi, A., Kenye, A., & Sahoo, S. S. (2020). Active role of community-managed forests in carbon sequestration. Environmental Monitoring and Assessment, 192, 1–15.
  31. Six, J., Conant, R. T., Paul, E. A., & Paustian, K. (2002). Stabilization mechanisms of soil organic matter. Plant and Soil, 241, 155–176.
  32. Sharma, S. (2016). District Census Handbook: Pakur, Jharkhand. Directorate of Census Operations, Government of India.
  33. Sileshi, G. W. (2014). A critical review of forest biomass estimation models, common mistakes and corrective measures. Forest Ecology and Management, 329, 237–254. https://doi.org/10.1016/j.foreco.2014.06.026
  34. Singh, P., Pandey, P., & Shukla, R. P. (2022). Sacred groves and their role in biodiversity conservation and ecosystem services in India. Environmental Conservation Journal, 23(1–2), 45–56.
  35. Tripathi, K. P., Chaudhary, L. B., & Tiwari, A. (2017). Litterfall and nutrient dynamics in tropical dry deciduous forests of India. Journal of Forestry Research, 28(4), 837–847. https://doi.org/10.1007/s11676-016-0321-0
  36. Upadhyay, T. P., Sankhayan, P. L., & Solberg, B. (2019). Carbon sequestration potential and cost-benefit analysis of community forests in Nepal. Forest Policy and Economics, 109, 102001. https://doi.org/10.1016/j.forpol.2019.102001
  37. Walkley, A., & Black, I. A. (1934). An examination of the Degtjareff method for determining soil organic matter and a proposed modification of the chromic acid titration method. Soil Science, 37(1), 29–38. https://doi.org/10.1097/00010694-193401000-00003
  38. Wildlife Institute of India (WII). (2020). Manual on carbon stock assessment and biodiversity monitoring in Indian forests. WII–MoEFCC, Government of India, Dehradun.
  39. Zanne, A. E., Lopez-Gonzalez, G., Coomes, D. A., Ilic, J., Jansen, S., Lewis, S. L., & Chave, J. (2009). Global wood density database. Dryad Digital Repository. https://doi.org/10.5061/dryad.234.

Photo
Sourav Chandra
Corresponding author

Divisional Forest Officer, Pakur Forest Division, Jharkhand, India.

Photo
Sanjay Xaxa
Co-author

Functional Area Expert, Central Mine Planning and Design Institute, Kanke Road, Ranchi, Jharkhand, India.

Photo
Ali Jabran
Co-author

Wildlife Expert, Pakur Forest Division, Jharkhand, India

Sourav Chandra*, Sanjay Xaxa, Ali Jabran, Carbon Storage and Sequestration Potential of Sacred Groves in Pakur District, Jharkhand, Int. J. Sci. R. Tech., 2026, 3 (3), 68-81. https://doi.org/10.5281/zenodo.18897902

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